Udo Vester


Ontology type: schema:Person     


Person Info

NAME

Udo

SURNAME

Vester

Publications in SciGraph latest 50 shown

  • 2019-01-21 HNF1B nephropathy has a slow-progressive phenotype in childhood—with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry in PEDIATRIC NEPHROLOGY
  • 2018-12 Author Correction: Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivo in SCIENTIFIC REPORTS
  • 2018-12 No evidence for point mutations in the novel renal cystine transporter AGT1/SLC7A13 contributing to the etiology of cystinuria in BMC NEPHROLOGY
  • 2017-12 Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivo in SCIENTIFIC REPORTS
  • 2017-11 Hämolytisch-urämisches Syndrom im Kindes- und Jugendalter in MONATSSCHRIFT KINDERHEILKUNDE
  • 2017-10 Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly in NATURE GENETICS
  • 2017-06 Dysurische Beschwerden bei einem syrischen Jungen in MONATSSCHRIFT KINDERHEILKUNDE
  • 2016-10 Comparison of different normalization strategies for the analysis of glomerular microRNAs in IgA nephropathy in SCIENTIFIC REPORTS
  • 2014-10 Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes in PEDIATRIC NEPHROLOGY
  • 2014-04 Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies in KIDNEY INTERNATIONAL
  • 2013-08 Long-term side effects of treatment with mTOR inhibitors in children after renal transplantation in PEDIATRIC NEPHROLOGY
  • 2013-04 Comprehensive analysis of glomerular mRNA expression of pro- and antithrombotic genes in atypical haemolytic-uremic syndrome (aHUS) in VIRCHOWS ARCHIV
  • 2010-06 Von Nierenzysten und Zystennieren in URO-NEWS
  • 2010-04 Von Nierenzysten und Zystennieren in PÄDIATRIE
  • 2010-02 The diagnostic value of ultrasound in cystic kidney diseases in PEDIATRIC NEPHROLOGY
  • 2010 Gefäßveränderungen nach Nierentransplantation im Kindesalter in GEFÄßERKRANKUNGEN IM KINDES- UND JUGENDALTER
  • 2008-10 Analysis of genes encoding laminin β2 and related proteins in patients with Galloway–Mowat syndrome in PEDIATRIC NEPHROLOGY
  • 2008-04 Cyclosporine-A-induced nephrotoxicity in children with minimal-change nephrotic syndrome: long-term treatment up to 10 years in PEDIATRIC NEPHROLOGY
  • 2007-11 Krankheiten nach Nierentransplantation in MONATSSCHRIFT KINDERHEILKUNDE
  • 2007-09 Current concepts in transplant surgery: laparoscopic living donor of the kidney in LANGENBECK'S ARCHIVES OF SURGERY
  • 2006-12 Decreased systemic bioavailability of L-arginine in patients with cystic fibrosis in RESPIRATORY RESEARCH
  • 2006-03 Oedema with proteinuria in Gambian children—a descriptive study in PEDIATRIC NEPHROLOGY
  • 2005-12 Search for mutations in SLC1A5 (19q13) in cystinuria patients in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2005-05 Sirolimus rescue of renal failure in children after combined liver-kidney transplantation in PEDIATRIC NEPHROLOGY
  • 2005-04 The response to cyclophosphamide in steroid-sensitive nephrotic syndrome is influenced by polymorphic expression of glutathion-S-transferases-M1 and -P1 in PEDIATRIC NEPHROLOGY
  • 2005-03 Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD) in KIDNEY INTERNATIONAL
  • 2004-11 Absorption phase cyclosporine (C2 h) monitoring in the first weeks after pediatric renal transplantation in PEDIATRIC NEPHROLOGY
  • 2004-11 Pathomechanisms and the diagnosis of arterial hypertension in pediatric renal allograft recipients in PEDIATRIC NEPHROLOGY
  • 2004-05 The population-specific distribution and frequencies of genomic variants in the SLC3A1 and SLC7A9 genes and their application in molecular genetic testing of cystinuria in UROLITHIASIS
  • 2004-05 Pseudotumor cerebri following cyclosporine A treatment in a boy with tubulointerstitial nephritis associated with uveitis in PEDIATRIC NEPHROLOGY
  • 2004-04 Everolimus in DRUGS
  • 2003-11 Significant contribution of genomic rearrangements in SLC3A1 and SLC7A9 to the etiology of cystinuria in KIDNEY INTERNATIONAL
  • 2003-07 Cyclophosphamide in steroid-sensitive nephrotic syndrome: outcome and outlook in PEDIATRIC NEPHROLOGY
  • 2003 Complications After Pediatric Liver Transplantation in DIAGNOSTIC AND INTERVENTIONAL RADIOLOGY IN LIVER TRANSPLANTATION
  • 2002-11 Severe Fusobacteria infections (Lemierre syndrome) in two boys in EUROPEAN JOURNAL OF PEDIATRICS
  • 2002-10 Cystinuria in children: Distribution and frequencies of mutations in the SLC3A1 and SLC7A9 genes in KIDNEY INTERNATIONAL
  • 2000-04 Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuria in PEDIATRIC NEPHROLOGY
  • 2000-01 Distal myopathy in nephropathic cystinosis in PEDIATRIC NEPHROLOGY
  • 1998-11 Non-compliance following renal transplantation in children and adolescents in PEDIATRIC NEPHROLOGY
  • 1998-02 End-stage renal failure in children younger than 6 years: renal transplantation is the therapy of choice in EUROPEAN JOURNAL OF PEDIATRICS
  • 1997-08 Urinary tract morbidity due to Schistosoma haematobium infection in Mali in KIDNEY INTERNATIONAL
  • 1995-04 Improved absorption of cyclosporin A from a new microemulsion formulation: implications for dosage and monitoring in PEDIATRIC NEPHROLOGY
  • 1994 Behandlungsalternativen bei Hemmkörperhämophilie B — Erfahrungen mit dem Einsatz von rekombinantem Faktor VIIa (rFVIIa) in 24. HÄMOPHILIE-SYMPOSION
  • 1985-09 Proteinuria, hematuria, and leukocyturia in children with mixed urinary and intestinal schistosomiasis in KIDNEY INTERNATIONAL
  • 1985-04 Circadian variation of ova excretion, proteinuria, hematuria, and leukocyturia in urinary schistosomiasis in KIDNEY INTERNATIONAL
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