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Es wurde 1 Person gefunden.
Funktionen
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Mitglied/er, Zentrum für Kinder- und Jugendmedizin
Aktuelle Veranstaltungen
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2024 SS
- Wahlfach: Spezielle Pädiatrie (PV)
- Urologisch-pädiatrisches Kolloquium
- Kinderheilkunde Blockpraktikum (PV)
- Nephrologisches Seminar (*)
- Kinderheilkunde Vorlesung Teil I (WA)
- Ausbildung Kinderklinik für den 3. klin. Studienabschnitt (WP)
- Kursus der allgemeinen pädiatrisch-klinischen Untersuchungen
- Anleitung zu wiss. Arbeiten für Mediziner und Naturwissenschaftler
Vergangene Veranstaltungen (max. 10)
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2023 WS
- Urologisch-pädiatrisches Kolloquium
- Tutorenausbildung
- Kinderheilkunde Blockpraktikum (PV)
- Wahlfach: Spezielle Pädiatrie (PV)
- Nephrologisches Seminar (*)
- Kursus der allgemeinen pädiatrisch-klinischen Untersuchungen
- Ausbildung Kinderklinik für den 3. klin. Studienabschnitt (WP)
- Kinderheilkunde Vorlesung Teil I (WA)
- Anleitung zu wiss. Arbeiten für Mediziner und Naturwissenschaftler
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2023 SS
Die folgenden Publikationen sind in der Online-Universitätsbibliographie der Universität Duisburg-Essen verzeichnet. Weitere Informationen finden Sie gegebenenfalls auch auf den persönlichen Webseiten der Person.
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Etiology of Kidney Diseases With Proteinuria in the Gambia/West AfricaIn: Frontiers in Pediatrics Jg. 10 (2022) 854719Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Nierenzysten und zystische Nierenerkrankungen bei Kindern (AWMF S2k-Leitlinie)In: Klinische Pädiatrie Jg. 232 (2020) Nr. 5, S. 228 - 248Online Volltext: dx.doi.org/
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Charakterisierung von Patienten mit atypischem hämolytisch-urämischen Syndrom (aHUS) in Deutschland : Daten aus dem globalen aHUS-RegisterIn: Der Nephrologe (2019)Online Volltext: dx.doi.org/ (Open Access)
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Erratum zu: Charakterisierung von Patienten mit atypischem hämolytisch-urämischen Syndrom (aHUS) in Deutschland: Daten aus dem globalen aHUS-RegisterIn: Der Nephrologe Jg. 14 (2019) Nr. 6, S. 505Online Volltext: dx.doi.org/ (Open Access)
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HNF1B nephropathy has a slow-progressive phenotype in childhood—with the exception of very early onset cases : results of the German Multicenter HNF1B Childhood RegistryIn: Pediatric Nephrology Jg. 34 (2019) Nr. 6, S. 1065 - 1075Online Volltext: dx.doi.org/ (Open Access)
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Author Correction : Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivoIn: Scientific Reports Jg. 8 (2018) Nr. 1, S. 6003Online Volltext: dx.doi.org/ (Open Access)
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No evidence for point mutations in the novel renal cystine transporter AGT1/SLC7A13 contributing to the etiology of cystinuriaIn: BMC Nephrology Jg. 19 (2018) Nr. 1, S. 278Online Volltext: dx.doi.org/ (Open Access)
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Dysurische Beschwerden bei einem syrischen JungenIn: Monatsschrift Kinderheilkunde Jg. 165 (2017) Nr. 6, S. 462 - 464Online Volltext: dx.doi.org/
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Glomerulocapillary miRNA response to HLA-class i antibody in vitro and in vivoIn: Scientific Reports Jg. 7 (2017) Nr. 1, S. 14554Online Volltext: dx.doi.org/ (Open Access)
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Hämolytisch-urämisches Syndrom im Kindes- und JugendalterIn: Monatsschrift Kinderheilkunde Jg. 165 (2017) Nr. 11, S. 1005 - 1018Online Volltext: dx.doi.org/
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Intermediate follow-up of pediatric patients with hemolytic uremic syndrome during the 2011 outbreak caused by E. Coli O104:H4In: Clinical Infectious Diseases (CID) Jg. 64 (2017) Nr. 12, S. 1637 - 1643Online Volltext: dx.doi.org/ (Open Access)
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Laudatio Prof. Dr. Karl-Heinz DeegIn: Ultraschall in der Medizin - European Journal of Ultrasound Jg. 38 (2017) Nr. 1, S. 98Online Volltext: dx.doi.org/
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Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney diseaseIn: Nature Genetics Jg. 49 (2017) Nr. 7, S. 1025 - 1034Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Mutations in KEOPS-complex genes cause nephritic syndrome with primary microcephalyIn: Nature Genetics Jg. 49 (2017) Nr. 10, S. 1529 - 1538Online Volltext: dx.doi.org/ (Open Access)
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Comparison of different normalization strategies for the analysis of glomerular microRNAs in IgA nephropathyIn: Sci Rep Jg. 6 (2016) S. 31992Online Volltext: dx.doi.org/ (Open Access)
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Combined liver and kidney transplantation and kidney after liver transplantation in children : Indication, postoperative outcome, and long-term resultsIn: Pediatric Transplantation Jg. 19 (2015) Nr. 8, S. 858 - 865Online Volltext: dx.doi.org/
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Pharmacological treatment of atypical hemolytic-uremic syndromeIn: Expert Opinion on Orphan Drugs Jg. 2 (2014) Nr. 2, S. 123 - 135Online Volltext: dx.doi.org/
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Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathiesIn: Kidney International Jg. 85 (2014) Nr. 4, S. 880 - 887Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD) : kidney-related and non-kidney-related phenotypesIn: Pediatric Nephrology Jg. 29 (2013) Nr. 10, S. 1915 - 1925Online Volltext: dx.doi.org/
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Complement Factor H–Related Protein 1 Deficiency and Factor H Antibodies in Pediatric Patients with Atypical Hemolytic Uremic SyndromeIn: Clinical Journal of the American Society of Nephrology Jg. 8 (2013) Nr. 3, S. 407 - 415Online Volltext: dx.doi.org/
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Comprehensive analysis of glomerular mRNA expression of pro- and antithrombotic genes in atypical haemolytic-uremic syndrome (aHUS)In: Virchows Archiv Jg. 462 (2013) Nr. 4, S. 455 - 464Online Volltext: dx.doi.org/
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Glomerular mRNA expression of prothrombotic and antithrombotic factors in renal transplants with thrombotic microangiopathyIn: Transplantation Jg. 95 (2013) Nr. 10, S. 1242 - 1248Online Volltext: dx.doi.org/
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Kidney grafts from donors ≤5 yr of age : Single kidney transplantation for pediatric recipients or en bloc transplantation for adults?In: Pediatric Transplantation Jg. 17 (2013) Nr. 2, S. 179 - 184Online Volltext: dx.doi.org/
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Long-term side effects of treatment with mTOR inhibitors in children after renal transplantationIn: Pediatric Nephrology Jg. 28 (2013) Nr. 8, S. 1293 - 1298Online Volltext: dx.doi.org/
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Seminal vesicle cysts and ipsilateral malformation of the kidney (Zinner's syndrome)In: Pediatric Nephrology Jg. 28 (2013) Nr. 8, S. 1403 - 1404
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An outbreak of shiga toxin-producing escherichia coli O104:H4 hemolytic uremic syndrome in Germany : presentation and short-term outcome in childrenIn: Clinical Infectious Diseases (CID) Jg. 55 (2012) Nr. 6, S. 753 - 759Online Volltext: dx.doi.org/ (Open Access)
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Donor and recipient ACE I/D genotype are associated with loss of renal function in children following renal transplantationIn: Pediatric Transplantation Jg. 15 (2011) Nr. 2, S. 214 - 220Online Volltext: dx.doi.org/
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Early renal failure after domino liver transplantation using organs from donors with primary hyperoxaluria type 1In: Transplantation Jg. 90 (2010) Nr. 7, S. 782 - 785Online Volltext: dx.doi.org/
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The diagnostic value of ultrasound in cystic kidney diseasesIn: Pediatric Nephrology Jg. 25 (2010) Nr. 2, S. 231 - 240Online Volltext: dx.doi.org/ (Open Access)
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Young Man With Kidney Failure and Hemorrhagic Interstitial NephritisIn: American Journal of Kidney Diseases Jg. 54 (2009) Nr. 6, S. 1162 - 1166Online Volltext: dx.doi.org/
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Continuous venovenous haemodialysis (CVVHD) in the acute management of neonatal hyperammonaemia : Experience in 14 neonatesIn: Pediatric Nephrology Jg. 22 (2007) Nr. 9, S. 1567Online Volltext: dx.doi.org/
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Unusual Manifestation of Posttransplant Lymphoproliferative Disorder in the EsophagusIn: Transplantation Proceedings Jg. 38 (2006) Nr. 3, S. 693 - 696Online Volltext: dx.doi.org/
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Oral L-arginine supplementation in cystic fibrosis patients : a placebo-controlled studyIn: European Respiratory Journal (ERJ) Jg. 25 (2005) Nr. 1, S. 62 - 68Online Volltext: dx.doi.org/
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Removal of metabolites, cytokines and hepatic growth factors by extracorporeal liver support in childrenIn: Journal of Pediatric Gastroenterology and Nutrition Jg. 40 (2005) Nr. 1, S. 54 - 59Online Volltext: dx.doi.org/
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Sirolimus rescue of renal failure in children after combined liver-kidney transplantationIn: Pediatric Nephrology Jg. 20 (2005) Nr. 5, S. 686 - 689Online Volltext: dx.doi.org/
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Pathomechanisms and the diagnosis of arterial hypertension in pediatric renal allograft recipientsIn: Pediatric Nephrology Jg. 19 (2004) Nr. 11, S. 1202 - 1211Online Volltext: dx.doi.org/
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Basiliximab in paediatric liver-transplant recipients [Kommentar)In: The Lancet Jg. 357 (2001) Nr. 9253, S. 388 - 389Online Volltext: dx.doi.org/
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Combined liver and kidney transplantation and kidney after liver transplantation in children : Indication, postoperative outcome, and long-term resultsIn: Pediatric Transplantation Jg. 19 (2015) Nr. Suppl. 1, Special Issue: IPTA 8th Congress on Pediatric Transplantation, S. 96Online Volltext: dx.doi.org/
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Histology and mRNA Expression : Insights Into the Pathophysiology of Thrombus Formation and Glomerular Remodeling in Thrombotic Microangiopathy in Renal TransplantsIn: Transplantation / 24th International Congress of the Transplantation Society; 15-19 July 2010; Berlin, Germany Jg. 94 (2012) Nr. 10S, S. 260Online Volltext: dx.doi.org/
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Kidneys from Pediatrics Donors <= 5 Year of Age are best used in Paediatric RecipientsIn: Transplant International Jg. 24 (2011) Nr. Suppl. 3, S. 10 - 11Online Volltext: dx.doi.org/
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Exercise-induced acute renal failure due to carnitine palmitoyltransferase II deficiencyIn: Pediatric Nephrology Jg. 24 (2009) Nr. 4, S. 918 - 919
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Steroid-Resistant Nephrotic SyndromeIn: Comprehensive Pediatric Nephrology / Geary, Denis F. (Hrsg.) 2008, S. 257 - 267Online Volltext: dx.doi.org/