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Organisation >> Universitätsklinikum Schleswig-Holstein (UK-SH), Campus Kiel >>

Klinik für Kinderonkologie und -rheumatologie

	2010 Effects of desmopressin on the sleep of children suffering from enuresis. Enuresis in hyperthyroidism: a temporary lack of central control mechanism leads to nocturnal enuresis.
	2007 A treatment protocol for infants younger than 1 year with acute lymphoblastic leukaemia (Interfant-99): an observational study and a multicentre randomised trial. Almost normal cognitive function in patients during therapy for childhood acute lymphoblastic leukemia without cranial irradiation according to ALL-BFM 95 and COALL 06-97 protocols: results of an Austrian-German multicenter longitudinal study and implications for follow-up. Classification of Distinct Baseline Insulin Infusion Patterns in Children and Adolescents With Type 1 Diabetes on Continuous Subcutaneous Insulin Infusion Therapy Clinical characteristics and treatment outcome of infants with non-Hodgkin lymphoma. Correction of compliance and resistance altered by endotracheal tube leaks and non-linear pressure/volume-relationships Effect of 1-desamino-8-D-arginine vasopressin on prepulse inhibition of startle supports a central etiology of primary monosymptomatic enuresis. Exclusion of Serum- and Glucocorticoid-Induced Kinase 1 (SGK1) as a Candidate Gene for Genetically Heterogeneous Renal Pseudohypoaldosteronism Type I in Eight Families. Gender role behavior in children with XY karyotype and disorders of sex development High interleukin-15 expression characterizes childhood acute lymphoblastic leukemia with involvement of the CNS Immunobiological diversity in infant acute lymphoblastic leukemia is related to the occurrence and type of MLL gene rearrangement. Incidence and outcome of TCF3-PBX1-positive acute lymphoblastic leukemia in Austrian children. Integrating molecular information into treatment of childhood acute lymphoblastic leukemia--a perspective from the BFM Study Group. Low-dose arsenic trioxide sensitizes glucocorticoid-resistant acute lymphoblastic leukemia cells to dexamethasone via an Akt-dependent pathway. Outcome of treatment in children with hypodiploid acute lymphoblastic leukemia. Pulses of vincristine and dexamethasone in addition to intensive chemotherapy for children with intermediate-risk acute lymphoblastic leukaemia: a multicentre randomised trial Relief of nocturnal enuresis by desmopressin is kidney and vasopressin type 2 receptor independent. Second allogeneic hematopoietic stem cell transplantation (HSCT) results in outcome similar to that of first HSCT for patients with juvenile myelomonocytic leukemia Secondary malignant neoplasms after intensive treatment of relapsed acute lymphoblastic leukaemia in childhood. The NQO1 C609T polymorphism is associated with risk of secondary malignant neoplasms after treatment for childhood acute lymphoblastic leukemia: a matched-pair analysis from the ALL-BFM study group.
	2006 A 10-year-old girl with bifocal synovial sarcoma Absence of exercise-induced leptin suppression associated with insufficient epinephrine reserve in patients with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Activating NOTCH1 mutations predict favorable early treatment response and long term outcome in child-hood precursor T-cell lymphoblastic leukemia. Analgetika / Sedativa Analyzing the functional and structural consequences of two point mutations (P94L, A368D) in the CYP11B1 gene causing congenital adrenal hyperplasia (CAH) due to 11-hydroxylase deficiency. Androgen receptor gene mutations in androgen insensitivity syndrome cause distinct patterns of reduced activation of androgen-responsive promoter constructs Antibiotika Arzneimitteltherapie und Ernährung im Kindesalter : Hinweise und Tipps für Klinik und Praxis Behavioural problems and autism in children with hydrocephalus : A population-based study Calcinosis cutis bei hereditärer Albright-Osteodystrophie = [Calcinosis cutis in Albright hereditary osteodystrophy Pseudohypoparathyroidism Type Ia.] Cell-line and tissue-specific signatures of androgen receptor-coregulator transcription Characterization and expression of CT45 in Hodgkin's lymphoma Chromosomal breakpoints affecting immunoglobulin Loci are recurrent in hodgkin and reed-sternberg cells of classical hodgkin lymphoma Consensus guidelines for microarray gene expression analyses in leukemia from three European leukemia networks Cytochrome c-related caspase-3 activation determines treatment response and relapse in childhood precursor B-cell ALL. Dauertherapie des Asthma bronchiale. Dendritic cell deficiencies in pediatric acute lymphoblastic leukemia patients. Diabetes mellitus Diagnosis and management of cerebral salt wasting (CSW) in children: the role of atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP). Die ambulant erworbene Pneumonie im Kindesalter Elucidating the underlying molecular pathogenesis of NR3C2 mutants causing autosomal dominant pseudohypoaldosteronism type 1. Epidemiology and Initial Management of Ambiguous Genitalia at Birth in Germany Folate metabolic gene polymorphisms and childhood acute lymphoblastic leukemia: a case-control study Four novel missense mutations in the CYP21A2 gene detected in Russian patients suffering from the classical form of congenital adrenal hyperplasia (CAH): identification, functional characterization and structural analysis Impact of cranial radiotherapy on central nervous system prophylaxis in children and adolescents with central nervous system-negative stage III or IV lymphoblastic lymphoma. In vivo effects of corticotropin-releasing hormone on femoral adipose tissue metabolism in women Inhalativa Initially elevated TSH and congenital central hypothyroidism due to a homozygous mutation of the TSH beta subunit gene: case report and review of the literature Intensivbehandlung bei akuten Läsionen des ZNS : Besonderheiten in Diagnostik und Therapie des Schädel-Hirn-Traumas bei Kindern Intrapulmonary application of a 5-lipoxygenase inhibitor using surfactant as a carrier reduces lung edema in a piglet model of airway lavage. Lack of expression of the chondroitin sulphate proteoglycan neuron-glial antigen 2 on candidate stem cell populations in paediatric acute myeloid leukaemia/abn(11q23) and acute lymphoblastic leukaemia/t(4;11). LEF-1 is crucial for neutrophil granulocytopoiesis and its expression is severely reduced in congenital neutropenia Long-term GnRH agonist treatment for female central precocious puberty does not impair reproductive function. MALT lymphoma in children: A report from the NHL-BFM study group. Mesoblastic nephroma--a report from the Gesellschaft fur Padiatrische Onkologie und Hamatologie (GPOH). Meta-analysis of inhaled nitric oxide in premature infants: an update. Minimal residual disease analysis in children with t(12;21)-positive acute lymphoblastic leukemia: comparison of Ig/TCR rearrangements and the genomic fusion gene. Mutational screen reveals a novel JAK2 mutation, L611S, in a child with acute lymphoblastic leukemia Neuroblastoma stage 4S with 123I-MIBG-positive bone marrow involvement. Novel human metapneumovirus sublineage Onkologie Over 15 years of ELTEC: A report of the international BFM study group. Parenterale Ernährung im Neugeborenen- und Kindesalter. Prognostic impact of age in children and adolescents with acute lymphoblastic leukemia: data from the trials ALL-BFM 86, 90, and 95. Recurrence of the R947X Mutation in Unrelated Families with Autosomal Dominant Pseudohypoaldosteronism Type 1: Evidence for a Mutational Hot Spot in the Mineralocorticoid Receptor Gene. Rituximab plus chemotherapy in children with relapsed or refractory CD20-positive B-cell precursor acute lymphoblastic leukemia. Superiority of allogeneic hematopoietic stem-cell transplantation compared with chemotherapy alone in high-risk childhood T-cell acute lymphoblastic leukemia: results from ALL-BFM 90 and 95 The A645D Mutation in the hinge region of the human AR gene modulates AR activity depending on the context of the polymorphic glutamine and glycine repeats. The Eighth International Childhood Acute Lymphoblastic Leukemia Workshop ('Ponte di legno meeting') report: Vienna, Austria, April 27-28, 2005. The MLL recombinome of acute leukemias. Therapievorschläge von A bis Z. Three novel point mutations of the CYP21 gene detected in classical forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Tissue-specific transcription profiles of sex steroid biosynthesis enzymes and the androgen receptor Unsupervised proteome analysis of human leukaemia cells identifies the Valosin-containing protein as a putative marker for glucocorticoid resistance. Wirkstoffe und Dosis von A bis Z
	2005 ABO-mismatched marrow transplantation: removal of mismatched donor red blood cells by "washing" with recipient's matched red blood cells in a closed system Akute lymphoblastische Leukämien Bronchoscopic Surfactant Administration in Pediatric Patients with Persistent Lobar Atelectasis Case report: successful interdisciplinary treatment of cerebrally disseminated invasive pulmonal aspergillosis in a child with acute myeloid leukemia Chemotherapy versus allogeneic transplantation for very-high-risk childhood acute lymphoblastic leukaemia in first complete remission: comparison by genetic randomisation in an international prospective study Chimaerism analyses and subsequent immunological intervention after stem cell transplantation in patients with juvenile myelomonocytic leukaemia Comparison of the BD Directigen Flu A+B Kit and the Abbott TestPack RSV with a multiplex RT-PCR ELISA for rapid detection of influenza viruses and respiratory syncytial virus Congenital adrenal hyperplasia due to 11-hydroxylase deficiency: functional characterization of two novel point mutations and a three-base pair deletion in the CYP11B1 gene Congenital adrenal hyperplasia in adulthood: do men need to continue treatment? Congenital adrenal hyperplasia: the molecular basis of 21-hydroxylase deficiency in H-2(aw18) mice CONGENITAL ISOLATED ACTH DEFICIENCY, AN UNDERESTIMATED CAUSE OF NEONATAL DEATH, EXPLAINED BY TPIT MUTATIONS Congenital lobar emphysema and increased nuchal translucency. Desmopression associated Symptomatic hyponatremic Hypervolemia in Children. Are there Predective Factors. Die deskriptive Epidemiologie von tiefen Atemwegsinfektionen bei Kindern im Raum Kiel Differences in infantile growth patterns in Turner syndrome girls with and without spontaneous puberty. Disproportionate stature but normal height in hypochondroplasia Early manifestation of calcinosis cutis in pseudohypoparathyroidism type Ia associated with a novel mutation in the GNAS gene Endoscopic third ventriculostomy in infants Functional characterization of two novel point mutations in the CYP21 gene causing simple virilizing forms of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. Gene-expression profiles and their association with drug resistance in adult acute myeloid leukemia Gonadotropin-releasing hormone analogue treatment for precocious puberty Homozygous disruption of P450scc (CYP11A1) is associated with prematurity, complete 46,XY sex reversal and severe adrenal failure. Impact of latent Epstein-Barr virus infection on outcome in children and adolescents with Hodgkin's lymphoma. Interferon alpha 2b treatment in an eleven-year-old boy with disseminated lymphangiomatosis Learning disabilities in a population-based group of children with hydrocephalus. Long-term outcome in children with relapsed ALL by risk-stratified salvage therapy: results of trial acute lymphoblastic leukemia-relapse study of the Berlin-Frankfurt-Munster Group 87 Long-term outcome in children with relapsed ALL by risk-stratified salvage therapy: results of trial acute lymphoblastic leukemia-relapse study of the Berlin-Frankfurt-Munster Group 87. MALT lymphoma in children: A report from the NHL-BFM study group Management of tectal glioma in childhood Molecular features and clinical phenotypes in androgen insensitivity syndrome in the absence and presence of androgen receptor gene mutations Myeloablative megatherapy with autologous stem-cell rescue versus oral maintenance chemotherapy as consolidation treatment in patients with high-risk neuroblastoma: a randomised controlled trial Neuroblastoma stage 4S with (123)I-MIBG-positive bone marrow involvement Population spectrum of ACADM genotypes correlated to biochemical phenotypes in newborn screening for medium-chain acyl-CoA dehydrogenase deficiency Population-based incidence of severe pneumonia in children in Kiel, Germany. Prognostic Impact of Age in Children and Adolescents with Acute Lymphoblastic Leukemia: Data from the Trials ALL-BFM 86, 90, and 95 = Prognostic Impact of Age in Children and Adolescents with Acute Lymphoblastic Leukemia: Data from the Trials ALL-BFM 86, 90, and 95 = [Alter als prognostischer Faktor bei Kindern und Jugendlichen mit akuter lymphoblastischer Leukämie : Ergebnisse aus den Therapiestudien ALL-BFM 86, 90 und 95] Proliferation characteristics in pediatric Hodgkin's lymphoma point to a cell cycle arrest in the G(1) phase. Proliferation rate and outcome in children with T-cell rich B-cell lymphoma: a clinicopathologic study from the NHL-BFM-study group Pubertas Praecox Salvage therapy of progressive and recurrent Hodgkin's disease: results from a multicenter study of the pediatric DAL/GPOH-HD study group. Salvage Therapy of progressive and Recurrent Hodgkin`s Disease: result from a multicenter study of the Pediatric DAL/GPOH-HD Study Group Serum cortisol and cortisone levels in newborns with congenital adrenal hyperplasia before the start of therapy. Surfactant reduces extravascular lung water and invasion of polymorphonuclear leukocytes into the lung in a piglet model of airway lavage. The eighth international childhood acute lymphoblastic leukemia workshop ('Ponte di Legno meeting') report: Vienna, Austria, April 27-28, 2005 The impact of age and gender on biology, clinical features and treatment outcome of non-Hodgkin lymphoma in childhood and adolescence The impact of cyclosporin A on acute graft-versus-host disease after allogeneic bone marrow transplantation in children and adolescents with acute lymphoblastic leukemia. The residue E351 is essential for the activity of human 21-hydroxylase: evidence from a naturally occurring novel point mutation compared with artificial mutants generated by single amino acid substitutions The seventh international childhood acute lymphoblastic leukemia workshop report: Palermo, Italy, January 29--30, 2005 Thiopurine methyltransferase (TPMT) genotype and early treatment response to mercaptopurine in childhood acute lymphoblastic leukemia Thirteen novel mutations in the NR0B1 (DAX1) gene as cause of adrenal hypoplasia congenita Topical inhibition of nuclear factor-kappaB enhances reduction in lung edema by surfactant in a piglet model of airway lavage. Topical interleukin-8 antibody attracts leukocytes in a piglet lavage model. Web-basiertes Frühwarnsystem zur Steuerung der RSV-Prävention im Kindesalter = [RSV-Prevention in Children Guided by a Web-Based Early Warning System]
	2004 A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutations. A Putative Sugar-Binding Transcriptional Regulator in a Novel Gene Locus in Enterococcus faecalis Contributes to Production of Biofilm and Prolonged Bacteremia in Mice. Acute lymphoblastic leukemia and Klinefelter syndrome in children: two cases and review of the literature Allogeneic peripheral blood stem cell transplantation following fludarabine-based conditioning in six children with advanced Hodgkin's disease. Autosomal-dominant pseudohypoaldosteronism type 1 in a Turkish family is associated with a novel nonsense mutation in the human mineralocorticoid receptor gene. Central reassessment of GH concentrations measured at local treatment centers in children with impaired growth: consequences for patient management. Comparative tolerability of drug treatment for nocturnal enuresis in children Congenital adrenal hyperplasia - how to improve the transition from adolescence to adult life. Congenital masses of the lung, cystic adenomatoid malformation versus congenital lobar emphysema: prenatal diagnosis and implications for postnatal treatment. DESMOPRESSIN HAS AN INFLUENCE ON THE AROUSABILITY OF CHILDREN WITH PRIMARY NOCTURNAL ENURESIS. Enterococcal infections: host response, therapeutic, and prophylactic possibilities Evaluation of a multiplex reverse transcriptase PCR ELISA for the detection of nine respiratory tract pathogens. Fatal Haemophilus influenzaetype b sepsis in a 10-month-old infant despite complete vaccination and adequate Hib antibodies. Fehldiagnose "Asthma bronchiale" bei Mediastinaltumor im Kindesalter : [Mediastinal tumour in children initially misdiagnosed and treated as bronchial asthma] Genetic heterogeneity in autosomal dominant pseudohypoaldosteronism type I: exclusion of claudin-8 as a candidate gene. INCREASED URINARY CALCIUM EXCRETION IN ENURETIC CHILDREN TREATED WITH DESMOPRESSIN. Konzept der Therapieoptimierungsstudie GPOH-HD 2003 für die Behandlung von Kindern und Jugendlichen mit einem Morbus Hodgkin: Evolution aus der Tradition der DAL/GPOH-Studien = The concept of the GPOH-HD 2003 therapy study for pediatric Hodgkin's disease: evolution in the tradition of the DAL/GPOH studies Language asymmetry and auditory attention in young adulthood after being born small-for-gestational age or with cardio-pulmonary resuscitation at birth. Long-term follow-up of spontaneous development in a boy with familial male precocious puberty. Longitudinal studies of molybdenum balances in breastfed infants Low occurrence of familial neuroblastomas and ganglioneuromas in five consecutive GPOH neuroblastoma treatment studies. Marked thrombocytosis in a child with advanced myelodysplastic syndrome. Morbus Hodgkin Mucosa-associated lymphoid tissue lymphoma in the conjunctiva of a child. Neuropsychological follow-up into young adulthood of term infants born small for gestational age Reduced-intensity conditioning prior to allogeneic transplantation of hematopoietic stem cells: the need for T cells early after transplantation to induce a graft-versus-lymphoma effect Rhabdomyosarkome Risk of sudden death in the Williams-Beuren syndrome. Serological and genetic diversity of capsular polysaccharides in Enterococcus faecalis The concept of the GPOH-HD 2003 therapy study for pediatric Hodgkin's disease: evolution in the tradition of the DAL/GPOH studies. The increased lysis of fetal cells in the mother after pregnancies complicated by pre-eclampsia or HELLP syndrome is not the result of a specific anti-fetal cytotoxicity of the mother Treatment and prevention of enterococcal infections--alternative and experimental approaches. Treatment of Pubertal Gynecomastia with the Specific Aromatase Inhibitor Anastrozole. Variables Explaining the Duration of Hospitalization in Children under Two Years of Age Admitted with Acute Airway Infections: Does Respiratory Syncytial Virus Have a Direct Impact? Visual attention in young adulthood after cardiopulmonary resuscitation at birth or being born small for gestational age Weighing diapers for intake assessment after early discharge Zinc concentration in human milk: longitudinal studies in consecutive lactation periods.
	2003 A Novel Claudin 16 Mutation Associated with Childhood Hypercalciuria Abolishes Binding to ZO-1 and Results in Lysosomal Mistargeting. An Outbreak of Rubella aboard a Ship of the German Navy. Antireflux or antiregurgitation milk products. Are needle-free injections a useful alternative for growth hormone therapy in children? Safety and pharmacokinetics of growth hormone delivered by a new needle-free injection device compared to a fine gauge needle. Arzneimitteltabellen Association of morphological characteristics with precocious puberty and/or gelastic seizures in hypothalamic hamartoma. Can respiratory syncytial virus etiology be diagnosed clinically? A hospital-based case-control study in children under two years of age. Chlamydien-Infektionen Chromatographic system for the simultaneous measurement of plasma 18-hydroxy-11-deoxycorticosterone and 18-hydroxycorticosterone by radioimmunoassay: reference data for neonates and infants and its application in aldosterone-synthase deficiency. Chronic interstitial lung disease with lung fibrosis in a girl : Uncommon sequelae of Epstein-Barr virus infection. Correction of compliance and resistance altered by endotracheal tube leaks. Die Porphyrien Gender-based differences in children with sepsis and ARDS: The ESPNIC ARDS Database Group Glia-to-neuron signaling and the neuroendocrine control of female puberty Glykogenspeicherkrankheiten Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency. Humanes Metapneumovirus in Deutschland nachgewiesen Identification of a novel mutation in the human mineralocorticoid receptor gene in a german family with autosomal-dominant pseudohypoaldosteronism type 1: further evidence for marked interindividual clinical heterogeneity. Interaktionen von Arzneistoffen Intestinal glucose transport: evidence for a membrane traffic-based pathway in humans. Krankheiten der Nebennieren Legionellose Leptospirose. Lymphome MLYCD mutation analysis: Evidence for protein mistargeting as a cause of MLYCD deficiency. Molecular analysis of the SGLT2 gene in patients with renal glucosuria Neutrophil aggregates in a 13-year-old girl: a rare hematological phenomenon. Normal female sexual development requires neuregulin-erbB receptor signaling in hypothalamic astrocytes Nutrient requirements for preterm infant formulas-molybdenum. Opsonophagocytic assay as a potentially useful tool for assessing safety of enterococcal preparations. Overexpression of glutamic acid decarboxylase-67 (GAD-67) in gonadotropin-releasing hormone neurons disrupts migratory fate and female reproductive function in mice. Partial response to biotin therapy in a patient with holocarboxylase synthetase deficiency: clinical, biochemical, and molecular genetic aspects. Pharmacokinetics and degree of aromatization rather than total dose of different preparations determine the effects of testosterone: a nonhuman primate study in Macaca fascicularis. Population-based burden of pneumonia before school entry in Schleswig-Holstein, Germany. Q-Fieber Selecting girls with precocious puberty for brain imaging: validation of European evidence-based diagnosis rule. Sepsis Tandem mass spectrometric determination of malonylcarnitine: diagnosis and neonatal screening of malonyl-CoA decarboxylase deficiency. The cellular immune response of children is specifically decreased against their parents but not vice versa, independent of pregnancy, age, or HLA or HY antigens The impact of peripartum factors on the onset and duration of lactation. The neurobiology of female puberty. Toxisches Schocksyndrom Two German CINCA (NOMID) patients with different clinical severity and response to anti-inflammatory treatment. Typhusschutzimpfung Virale Atemwegsinfektionen mit saisonaler Häufung bei Kindern : eine Übersicht mit Schwerpunkten auf Daten aus Deutschland von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP. Web-basiertes Frühwarnsystem : das infektionsepidemiologische Forschungsnetz PID-ARI.Net untersucht akute respiratorische Infektionen im Kindesalter.
	2002 A secondary respiratory chain defect in a patient with Fanconi-Bickel syndrome. Activation of A-type gamma-aminobutyric acid receptors excites gonadotropin-releasing hormone neurons. Adult height after GH therapy in 188 Ullrich-Turner syndrome patients: results of the German IGLU Follow-up Study 2001. Burden of Disease in Hospitalized RSV-positive Children in Germany Cardiolipin deficiency in X-linked cardioskeletal myopathy and neutropenia (Barth syndrome, MIM 302060): a study in cultured skin fibroblasts. Central precocious puberty in girls with Williams syndrome. Combined treatment with testosterone (T) and ethinylestradiol (EE2) in constitutionally tall boys: is treatment with T plus EE2 more effective in reducing final height in tall boys than T alone? Complete virilization in congenital adrenal hyperplasia: clinical course, medical management and disease-related complications. Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society. Consensus Statement on 21-Hydroxylase Deficiency from the Lawson Wilkins Pediatric Endocrine Society and The European Society for Pediatric Endocrinology Desmopressin for nocturnal enuresis in nephrogenic diabetes insipidus. Detection and Correction of Endotracheal-Tube Position in Premature Neonates Differentiation of single populations in a bidirectional mixed lymphocyte culture using X and Y chromosome-specific FiSH markers. Elevated blood drug levels obtained from indwelling silicon catheters during oral cyclosporine A administration. Epiglottopexy for the treatment of severe laryngomalacia. Epithelial Ca(2+) channel (ECAC1) in autosomal dominant idiopathic hypercalciuria. Fanconi-Bickel syndrome--a congenital defect of facilitative glucose transport. Feeding patterns in breast-fed and formula-fed infants. Follow-up into young adulthood after cardiopulmonary resuscitation in term and near-term newborn infants. I. Educational achievements and social adjustment. Follow-up into young adulthood after cardiopulmonary resuscitation in term and near-term newborn infants. II. Neuropsychological consequences. Hemolytic uremic syndrome due to an altered factor H triggered by neonatal pertussis. Hochauflösende Computertomographie der Lunge im Kindesalter : [High-resolution computed tomography of the lungs in pediatric patients] Large variability in performance IQ associated with postnatal morbidity, and reduced verbal IQ among school-aged children born preterm. Long-term suppression of pituitary-gonadal function with three-month depot of leuprorelin acetate in a girl with central precocious puberty. Longitudinal study of plasma pregnenolone and 17-hydroxypregnenolone in full-term and preterm neonates at birth and during the early neonatal period. Management and outcome of central precocious puberty. Management of congenital adrenal hyperplasia: results of the ESPE questionnaire. Metabolismus von Dehydroepiandrosteron durch Epidermophyton floccosum : [Dehydroepiandrosterone metabolism by Epidermophyton floccosum] Multiplex Minisequencing of the 21-Hydroxylase Gene as a Rapid Strategy to Confirm Congenital Adrenal Hyperplasia Nocturnal enuresis in patients with nephrogenic diabetes insipidus. Prevention of oestradiol-associated toxicosis in a dalmatian by early intervention with granulocyte colony-stimulating factor. Rapid molecular discrimination between infection with wild-type varicella-zoster virus and varicella vaccine virus. Repyloromyotomy for Recurrent Infantile Hypertrophic Pyloric Stenosis after sucessful first Pyloromyotomy Screening for Turner's syndrome by chromosome analysis of all girls with short stature. Seasonality of respiratory syncytial virus-positive hospitalizations in children in Kiel, Germany, over a 7-year period. Supplemental feeding in the first days of life -- effects on the recipient infant. Synchronous detection of a pulmonary papillary adenoma and lung metastases in a patient with osteosarcoma in relapse. Tetrahydrobiopterin responsiveness in phenylketonuria. Two new cases and a review of molecular genetic findings. The incidence of influenza-associated hospitalizations in children in Germany. The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome. Treatment of central precocious puberty. Über die mindere Qualität von Nierensonogrammen bei Patienten mit lumbaler Meningomyelozele : [On the Inferior Quality of Renal Sonograms in Patients with Lumbar Meningomyelozele] What's new in enuresis?
	2001 A case of fetal parvovirus B19 myocarditis, terminal cardiac heart failure, and perinatal heart transplantation. Alters- und gewichtsbezogene Dosierung von dDAVP in der Therapie der primären Enuresis nocturna : [Age- and Weight-related Dosage of dDAVP in the Treatment of Primary Nocturnal Enuresis] Alveolar recruitment promotes homogeneous surfactant distribution in a piglet model of lung injury. Automated chromatographic system for the simultaneous measurement of plasma pregnenolone and 17-hydroxypregnenolone by radioimmunoassay. Calcitriol controls the epithelial calcium channel in kidney. Detection of Epstein-Barr virus DNA in peripheral blood of paediatric patients with Hodgkin's disease by real-time polymerase chain reaction. Effect of glucocorticoid excess on the cortisol/cortisone ratio. Evidence for Genetic Heterogeneity of Pseudohypoaldosteronism Type 1 : Identification of a Novel Mutation in the Human Mineralocorticoid Receptor in one Sporadic Case and No Mutations in Two Autosomal Dominant Kindreds Evolution of cortisol/cortisone metabolism in infancy Familial Williams-Beuren syndrome showing varying clinical expression. Functional residual capacity determines the effect of inhaled nitric oxide on intrapulmonary shunt and gas exchange in a piglet model of lung injury. Hand-Mund-Fuss-Krankheit und Häufigkeitszunahme. Holoprosencephaly and low molecular weight proteinuria: the human homologue of murine megalin deficiency. Hyperinsulinism in syndromal disorders. Incidence of respiratory syncytial virus-positive hospitalizations in Germany. Interaktionen von Arzneistoffen. Laboratory signs of activated coagulation are common in Henoch-Schonlein purpura. Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation. Lymphome. Metacarpophalangeal pattern profile (MCPP) analysis in Williams-Beuren Syndrome (WBS). Molecular genetic basis and prevalence of glycogen storage disease type IIIA in the Faroe Islands. Molybdenum balance studies in premature male infants. Molybdenum in infancy : methodical investigation of urinary excretion. Molybdenum in infancy: balance studies in patients with intestinal stomata. Molybdenum metabolism: stable isotope studies in infancy. Molybdenum supply of very low-birth-weight premature infants during the first months of life. Mütterliche Belastung bei Kindern mit Williams-Beuren-Syndrom, Down-Syndrom, geistiger Behinderung nichtsyndromaler Ätioligie im Vergleich zu der nichtbehinderter Kinder. : [Maternal stress among mothers of children with Williams-Beuren syndrome, Down's syndrome and mental retardation of non-syndromal etiology in comparison to mothers of non-disabled children] Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndrome. Oral mature teratoma containing epididymal tissue in a female neonate. Pathogenesis and epidemiology of precocious puberty. Effects of exogenous oestrogens. Plasma selenium in preterm and term infants during the first 12 months of life. Prolonged dietary calcium restriction: a diagnostic approach in idiopathic hypercalciuria. Radiological case of the month. Denouement and discussion: congenital esophageal duplication cyst as a rare cause of neonatal progressive stridor. Response to inhaled nitric oxide in premature and term neonates. Sensitive and rapid quantification of busulfan in small plasma volumes by liquid chromatography-electrospray mass spectrometry. Special feature: picture of the month. Infantile scurvy. The effect of desmopressin on short-term memory in children with primary nocturnal enuresis.
	2000 A new simple method of staining exogenous surfactant in experimental research. Adult patients with Prader-Willi syndrome: clinical characteristics, life circumstances and growth hormone secretion. Age effects in dichotic listening to consonant-vowel syllables: interactions with attention. Änderungen der Nasenschleimhautdurchblutung bei infektanfälligen Kindern nach einer Klimakur an der See. Angeborene Störungen des Glukose-Transportes (review). Anorexia nervosa in congenital adrenal hyperplasia: long-term follow-up of 4 cases. Applicability of different antibodies for immunohistochemical localization of CFTR in sweat glands from healthy controls and from patients with cystic fibrosis. Candida arthritis in a premature infant treated successfully with oral fluconazole for six months. Chest physiotherapy in mechanically ventilated children: a review. Clinical, endocrine, and molecular genetic findings in patients with 17beta-hydroxysteroid dehydrogenase deficiency. Comparison of noise levels caused by four different neonatal high-frequency ventilators. DiGeorge syndrome with discordant phenotype in monozygotic twins. Early tubular proteinuria and development of nephritis in Henoch-Schönlein purpura. Effective elimination of carbon dioxide by nasopharyngeal high-frequency ventilation. Epidemiological investigation of nine respiratory pathogens in hospitalized children in Germany using multiplex reverse-transcriptase polymerase chain reaction. Epidemiology of pneumococcal disease in children in Germany. Epithelial calcium channel: gate-keeper of active calcium reabsorption. Epstein-Barr virus-associated post-transplant lymphoproliferative disease after bone marrow transplantation mimicking graft-versus-host disease. Equal distribution of congenital blood cell chimerism in dizygotic triplets after in-vitro fertilization. Evidence for change of 11beta-hydroxysteroid dehydrogenase activity during infancy and childhood. Gene structure and chromosomal mapping of human epithelial calcium channel. Hereditary fructose intolerance and alpha(1) antitrypsin deficiency. Immunogenicity and reactogenicity of the Biken acellular pertussis vaccine in young adults. Impfungen und reisemedizinisch relevante Empfehlungen für Organtransplantierte : [Vaccinations and medical recommendations for patients traveling after organ transplantation] Improvement in respiratory compliance after surfactant therapy evaluated by a new method. Inhalative Stickstoffmonoxidtherapie bei Frühgeborenen : [Inhaled nitric oxide therapy in preterm infants] Inhaled nitric oxide in premature infants--a meta-analysis. Longitudinal analysis of growth over the first 3 years of life in Turner's syndrome. Magnesium balance studies in premature and term infants. Molecular analysis in glycogen storage disease 1 non-A: DHPLC detection of the highly prevalent exon 8 mutations of the G6PT1 gene in German patients. Molecular cloning, tissue distribution, and chromosomal mapping of the human epithelial Ca2+ channel (ECAC1). Molybdenum supplementation in phenylketonuria diets: adequate in early infancy? Paraneoplastic cerebellar degeneration in pediatric Hodgkin disease. Pitfalls in the immunohistochemical localization of the cystic fibrosis transmembrane conductance regulator in paraffin embedded sweat glands. Postoperative Mycobacterium avium osteomyelitis confirmed by polymerase chain reaction. Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany. Primary vaccination of infants with diphtheria-tetanus-acellular pertussis-hepatitis B virus- inactivated polio virus and Haemophilus influenzae type b vaccines given as either separate or mixed injections. Proportion of invasive pneumococcal infections in Germann children preventable by pneumococcal conjugate vaccines. Pseudotumor cerebri induced by all-trans-retinoic acid in a child treated for acute promyelocytic leukemia. Reduced-intensity allogeneic stem cell transplantation as salvage treatment for patients with indolent lymphoma or CLL after failure of autologous SCT. Scrotal temperature is increased in disposable plastic lined nappies. The neurobiology of female puberty Therapie des Kleinwuchses mit Wachstumshormon : Entwicklungen 10 Jahre nach Einführung von rekombinantem Wachstumshormon. Timing of surfactant administration determines its physiologic response in a rabbit model of airway lavage. Transorale Behandlung der schweren Laryngomalazie. Ubersicht und Beschreibung einer modifizierten Operationstechnik : [Transoral treatment of severe laryngomalacia. Review and presentation of a modified surgical technique] Treatment of central precocious puberty: lessons from a 15 years prospective trial. German Decapeptyl Study Group. Williams-Beuren syndrome 35 years after the diagnosis in one of the first Beuren patients. Zinc intakes and plasma concentrations in infancy.
	1999 A novel frameshift mutation (141delT) in exon 1 of the 21-hydroxylase gene (CYP21) in a patient with the salt wasting form of congenital adrenal hyperplasia. Mutation in brief no. 255. Online. Accidental overdose of vancomycin in preterm twins. Akutes Fieber bei Tropenrückkehrern. Autografting of highly purified peripheral blood progenitor cells following myeloablative therapy in patients with lymphoma: a prospective study of the long-term effects on tumor eradication, reconstitution of hematopoiesis and immune recovery. Celiac disease and selective IgA deficiency in a girl with atypical Turner syndrome. Cellular immune response of a varicella vaccine following simultaneous DTaP and VZV vaccination. Chronisches Fieber bei Tropenrückkehrern. Clinical and molecular spectrum of somatic mosaicism in androgen insensitivity syndrome. Decrease in lung volume depends on end-expiratory pressure in a rabbit model of airway lavage. DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis. Disorders of the aldosterone synthase and steroid 11beta-hydroxylase deficiencies. Effect of DDAVP on nocturnal enuresis in a patient with nephrogenic diabetes insipidus. Effizienz und Risiken der Atemphysiotherapie beim Neugeborenen - Übersicht über die Literatur [Efficiency and risk of chest physiotherapy in the newborn--review of the literature] Evaluation of a single-sample serological technique for diagnosing pertussis in unvaccinated children. Fatal rupture of a sacrococcygeal teratoma during delivery. Gegen Varizellen impfen? Gonadal histology with testicular carcinoma in situ in a 15-year-old 46,XY female patient with a premature termination in the steroidogenic acute regulatory protein causing congenital lipoid adrenal hyperplasia. Growth retardation in Turner syndrome: aneuploidy, rather than specific gene loss, may explain growth failure. Impfungen bei Kindern mit fehlender oder geschwaechter Immunabwehr. Inappropriate secretion of natriuretic peptides in a patient with a cerebral tumor. Influence of hyperfiltration on the measurement of urinary N-acetyl-beta-D-glucosaminidase. Leuprorelindepot zur Behandlung der progressiven Pubertas praecox vera. Long-term outcome after depot gonadotropin-releasing hormone agonist treatment of central precocious puberty: final height, body proportions, body composition, bone mineral density, and reproductive function. Longitudinal evaluation of growth, puberty, and bone maturation in children with Williams syndrome. Mast cells contribute to PACAP-induced dermal oedema in mice. Microencapsulated NaCl for oral salt-replacement therapy in infants. Morphine induced allodynia in a child with brain tumour. Observer bias in acellular pertussis vaccine trials. Pubertätszeichen beim männlichen Säugling. Rapid identification of nine microorganisms causing acute respiratory tract infections by single-tube multiplex reverse transcription-PCR: feasibility study. Regulation of arginine vasopressin in enuretic children under fluid restriction. Serum leptin levels in patients with progressive central precocious puberty. Stem cell factor influences neuro-immune interactions: the response of mast cells to pituitary adenylate cyclase activating polypeptide is altered by stem cell factor. Störung der Pubertät The wide spectrum of clinical expression in Adams-Oliver syndrome: a report of two cases. Treatment of hyperinsulinaemic hypoglycaemia with nifedipine. Tubulointerstitial nephritis and uveitis in association with Epstein-Barr virus infection.
	1998 A mutation in the first transmembrane domain of the lutropin receptor causes male precocious puberty. A New Method to Analyze Lung Compliance when Pressure Volume Relationship is Non Linear : Letters to the Editor A new method to analyze lung compliance when pressure-volume relationship is nonlinear. A serologic study of organisms possibly associated with pertussis-like coughing. Änderungen des immunglobulins a im speichel von kindern nach einer Klimakur an der Nordsee. Androgens and fetal growth. Arzneimitteltherapei und Ernährung im Kindesalter : Hinweise und Tips für Klinik und Praxis. Clinical deterioration after cessation of growth hormone replacement therapy in a young adult with severe growth hormone deficiency. Comparison of different strategies of molecular genetic monitoring following autologous stem cell transplantation in patients with follicular lymphoma. Comprehensive analytical strategy for mutation screening in 21-hydroxylase deficiency. Congenital adrenal hypoplasia : clinical spectrum, experience with hormonal diagnosis, and report on new point mutations of the DAX-1 gene. Der Verhaltensphänotyp beim Williams-Beuren-Syndrom : Darstellung des aktuellen Forschungsstandes. Effect of inhaled nitric oxide on intrapulmonary right-to-left-shunting in two rabbit models of saline lavage induced surfactant deficiency and meconium instillation. Effect of therapeutic concentrations of nitric oxide on bacterial growth in vitro. Efficacy of the subcutaneous reformulated triptorelin depot in children with central precocious puberty. Enhancement of surfactant effect by a mechanical volume recruitment maneuver depends on the lungs preexisting distension. Fanconi-Bickel syndrome--a congenital defect of the liver-type facilitative glucose transporter. SSIEM Award. Society for the Study of Inborn Errors of Metabolism. Fanconi-Bickel syndrome--the original patient and his natural history, historical steps leading to the primary defect, and a review of the literature. Further evidence for a dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy: a family with documented hyperinsulinemia in two generations. High-frequency ventilation augments the effect of inhaled nitric oxide in persistent pulmonary hypertension of the newborn. Homozygous deletion of arginine-173 in the CYP11B2 gene in a girl with congenital hypoaldosteronism. Corticosterone methyloxidase deficiency type II. Hypercalciuria and nephrocalcinosis in a patient receiving long-term parenteral nutrition: the effect of intravenous chlorothiazide. Improvement of lung compliance after administration of bovine surfactant. Intracerebral hemorrhage as a late complication after CNS treatment of childhood lymphoma. Molecular genetic study in two patients with congenital hypoaldosteronism (types I and II) in relation to previously published hormonal studies. Mutation THR-185 ILE is associated with corticosterone methyl oxidase deficiency type II. Nephrocalcinosis in three siblings with idiopathic hypercalciuria. Partial transsection of the neonatal trachea. Rate of surfactant administration influences lung function and gas exchange in a surfactant-deficient rabbit model. Surfactanttherapie bei Atemnotsyndrom - aber wie? : eine Übersicht. Synergismus von inhalativem Stickstoffmonoxid und Hochfrequenzbeatmung bei der Therapie des Mekoniumaspirationssyndrome Synergistic effects of high-frequency ventilation and inhaled nitric oxide in the treatment of hypoxemic respiratory failure in infancy. Transitorische Pubertas praecox vera. Treatment of respiratory failure with inhaled nitric oxide and high- frequency ventilation in an infant with respiratory syncytial virus pneumonia and bronchopulmonary dysplasia. Variation of inhaled nitric oxide concentration with the use of a phasic flow ventilator. Williams-Beuren Syndrom : Spätdiagnose bei einem 24-jährigen Mann.
	1997 A higher rate of hyperandrogenic disorders in female-to-male transsexuals. Akzidentelle Stechapfelintoxikation : Verwechslung mit einer exotischen Frucht Allogeneic peripheral blood progenitor cells for treatment of relapse after bone marrow transplantation. Anastomosis of the umbilical arteries: physiologic variant or complication of umbilical catheterization? Anthropometrical measurements and androgen levels in males, females, and hormonally untreated female-to-male transsexuals. Blood on filter paper as a readily available source of bcr-abl rearranged mRNA. Cell-mediated immunity after pertussis vaccination and after natural infection. Dichotic listening performance and intracarotid amobarbital injections in children/adolescents : Comparisons pre- and post-operatively. Die Betreuung des hypogonadalen männlichen Patienten im Übergang zum Erwachsenalter. Effect of volume recruitment on response to surfactant treatment in rabbits with lung injury. Epstein-Barr virus-associated Hodgkin's disease: epidemiologic characteristics in international data. Evidence for endocrinological abnormalities in heterozygotes for adrenal 11 beta-hydroxylase deficiency of a family with the R448H mutation in the CYP11B1 gene. Evidence for induction of polysaccaride-specific B-cell memory in the first year of life: plain Haemophilus influenzae type b-PRP as a booster in children primed with a tetanus conjugate Hib-vaccine mixed with a combined diphtheria-tetanus-acellular pertussis-hepatitis B vaccine. Fanconi-Bickel syndrome presenting in neonatal screening for galactosaemia. Growth promotion and Turner-specific bone age after therapy with growth hormone and in combination with oxandrolone: when should therapy be started in Turner syndrome? Hereditary defect in biosynthesis of aldosterone: aldosterone synthase deficiency 1964-1997. Impaired macrophage listericidal and cytokine activities are responsible for the rapid death of Listeria monocytogenes-infected IFN-gamma receptor-deficient mice. Längsschnittstudie zur neuropsychologischen Entwicklung blinder früh- und reifgeborener Kinder Longitudinal study of neuropsychological outcome in blind extremely-low-birthweight children. Magnetic resonance imaging of the brain in Williams-Beuren syndrome. memory for words and drawings in children with hemiplegic cerebral palsy." Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome. Neue Impfstrategie gegen Poliomyelitis : Lebend-Vakzine oder inaktivierte Vakzine? Neue Wege im Einsatz von Kortikosteroiden bei pulmonalen Erkrankungen des Frühgeborenen. Oxalate excretion during the first 7 weeks in very-low-birth-weight infants. Personality characteristics and behaviour problems in individuals of different ages with Williams syndrome. Picture of the Month : Williams-Beuren syndrome. Polymersaekettenreaktion, die : [Polymerase chain reaction] Relevance of major histocompatibility complex class II expression as a hallmark for the cellular differentiation in the human adrenal cortex. Safety and efficacy of acellular pertussis vaccines: the Mainz study and other recent studies. The identification of hyperoxaluria in very low-birthweight infants--which urine sampling method? The identification of hyperoxaluria in very low-birthweight infants--which urine sampling method? The influence of mode of delivery on hematologic values in the umbilical vein. Umkehr eines Rechts-Links-Shunts und dauerhafte Verbesserung der Oxygenierung durch Inhalation von Stickstoffmonoxyd (NO) bei einem Frühgeborenen mit Lungenhypoplasie und asphyxie [Reversal of a right-left shunt and permanent improvement of oxygenation by inhalation of nitrogen monoxide in a premature infant with lung hypoplasia and asphyxia] Visualization of injection depot after subcutaneous administration by syringe and needle-free device (Medi-Jector): first results with magnetic resonance imaging.
	1996 A novel missense (E163G) mutation in the catalytic subunit of lipoprotein lipase causes familial chylomicronemia. Acellular pertussis vaccines: the final countdown. Acellular pertussis vaccines: the rationale for an efficacy trial in Germany. Autism and epilepsy (and tubereous sclerosis?) in the two pre-adolescent boys: Neuropsychiatric aspects before and after epilepsy surgery. Autism and epilepsy (and tubereous sclerosis?) in two pre-adolescent boys: Neuropsychiatric aspects before and after epilepsy surgery. Candida species infections. Cerebrospinal fluid concentrations of leukotriene B4 in bacterial meningitis. Children with benign focal sharp waves in the EEG--developmental disorders and epilepsy. Congenital hypoaldosteronism: the Visser-Cost syndrome revisited. Dichotic Listening Performance in a Monozygotic Twin-pair with Left- and Right-sided Hemiplegia. Die Behandlung der chronisch myeloischen Leukämie bei Kindern und Jugendlichen : Konzept der myelizentrischen Pilotstudie CML -päd-. [Treatment of chronic myeloid leukemia in children and adolescents--concept of the multicenter pilot study CML-ped.] Efficacy of acellular pertussis vaccine in early childhood after household exposure. Geographic distribution and origin of CFTR mutations in Germany. Geschlechtsidentitaetsstoerungen bei kindern und jugendlichen. Hepatopathie bei Patienten mit Neuroblastom Stadium 4S : [Hepatopathy in patients with stage 4S neuroblastoma] Hyporeninaemic hypoaldosteronism after growth hormone treatment. Incidence and spectrum of renal abnormalities in Williams-Beuren syndrome. Inhalative Stickoxid (NO)- Therapie bei Neugeborenen : Responder und Nonresponder. Morbidity and mortality of discordant twins up to 34 weeks of gestational age. Neues über Pertussis und Pertussis-Impfstoffe. Patient-triggered ventilation: a comparison of tidal volume and chestwall and abdominal motion as trigger signals. Persistierender Perikarderguß Pertussis-specific cell mediated immunity in infants after vaccination with a tricomponent acellular pertussis vaccine. Physiological bowlegs or infantile Blount's disease. Some new aspects on an old problem. Precast commercial polyacrylamide gels for separation of DNA amplificates by temperature gradient gel electrophoresis: application to clonality analysis of lymphomas. Prenatal diagnosis of congenital adrenal hypoplasia. Unusual complex of ventral midline anomalies: a multiple congenital anomalies/mental retardation syndrome Williams-Beuren syndrome and celiac disease. Wirksamkeit der BCG-Impfung.
	1995 Antidiuretic hormone regulation in patients with primary nocturnal enuresis. Decreased activity of respiratory-chain enzymes in glutaric aciduria type II. Discordance for hyperinsulinemic hypoglycemia in monozygotic twins. Häufiges Wenden ikterischer Neugeborener während der Phototherapie.
	1994 Association of malonyl-CoA decarboxylase deficiency and heterozygote state for haemoglobin C disease. Natural history of body mass index in Williams-Beuren syndrome.
	1993 [Comparison between complete and incomplete suppression of the hypophyseal-gonadal axis in girls with central precocious puberty: effect on growth and prospective final height] [Williams-Beuren syndrome in combination with celiac disease] Amplification of a Y-chromosomal DNA sequence by the polymerase chain reaction for documentation of residual recipient cells in small samples from bone marrow, peripheral blood and cerebrospinal fluid after bone marrow transplantation. Comparison of complete and incomplete suppression of pituitary-gonadal activity in girls with central precocious puberty: influence on growth and predicted final height. The German-Dutch Precocious Puberty Study Group. Comparison of umbilical arterial versus umbilical venous blood pH correlated with arterio-venous glucose difference and cardiotocographic score. Faecal excretion in infants. Isolated defect of peroxisomal beta-oxidation in a 16-year-old patient. Monitoring of chimerism after allogeneic bone marrow transplantation with unmanipulated marrow by use of DNA polymorphisms.
	1992 Growth, bone maturation and height prediction after three years of therapy with the slow release GnRH-agonist Decapeptyl-Depot in children with central precocious puberty. Hypothalamic-pituitary-gonadal function in two infants with Smith-Lemli-Opitz syndrome. Longitudinal zinc balances in breast-fed and formula-fed infants. Statural growth in Williams-Beuren syndrome.
	1991 [Long-term therapy with delayed-action LHRH-antagonist decapeptyl depot in girls with precocious puberty. Results of an international multicenter study] Iron availability from an infant formula supplemented with bovine lactoferrin. Remission of juvenile chronic myeloid leukemia following graft failure of an unrelated marrow transplant and autologous recovery of marrow function promoted by GM-CSF and IL-3. Successful stimulation of autologous bone marrow recovery by GM-CSF and IL-3 after an unrelated donor BMT for juvenile CML complicated by graft failure. The steroid hormonal milieu of the undisturbed human fetus and mother at 16-20 weeks gestation.
	1990 Arterielle Thrombose bei einem Frühgeborenen : [Arterial thrombosis in a premature infant] Reference ranges of lutropin and follitropin in the luliberin test in prepubertal and pubertal children using a monoclonal immunoradiometric assay. Selenium balances in young infants fed on breast milk and adapted cow's milk formula. Trace element excess in PKU diets? Urinary zinc excretion in infancy.
	1989 Fractionated total body irradiation plus high-dose VP-16 prior to allogeneic bone marrow transplantation in children with poor risk acute leukaemias. Lissencephaly, abnormal lymph nodes, and T-cell deficiency in one patient. Longitudinal manganese and copper balances in young infants and preterm infants fed on breast-milk and adapted cow's milk formulas.



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