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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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WiSe 2025
- Wahlfach: Spezielle Pädiatrie (PV)
- Urologisch-pädiatrisches Kolloquium
- Kinderheilkunde Blockpraktikum (PV)
- Tutorenausbildung
- Nephrologisches Seminar (*)
- Ausbildung Kinderklinik für den 3. klin. Studienabschnitt (WP)
- Kinderheilkunde Vorlesung Teil I (WA)
- Kursus der allgemeinen pädiatrisch-klinischen Untersuchungen
- Anleitung zu wiss. Arbeiten für Mediziner und Naturwissenschaftler
Vergangene Veranstaltungen (max. 10)
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SoSe 2025
- Urologisch-pädiatrisches Kolloquium
- Kinderheilkunde Blockpraktikum (PV)
- Nephrologisches Seminar (*)
- Wahlfach: Spezielle Pädiatrie (PV)
- 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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WiSe 2024
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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Evidenz- und konsensbasierte (S3) Leitlinie : Management der Urethritis bei männlichen* Jugendlichen und ErwachsenenIn: Journal der Deutschen Dermatologischen Gesellschaft (JDDG), Jg. 23, 2025, Nr. 2, S. 254 – 276DOI (Open Access)
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German evidence- and consensus-based guideline on the management of penile urethritisIn: Journal der Deutschen Dermatologischen Gesellschaft (JDDG), Jg. 23, 2025, Nr. 2, S. 254 – 275DOI (Open Access)
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Etiology of Kidney Diseases With Proteinuria in the Gambia/West AfricaIn: Frontiers in Pediatrics, Jg. 10, 2022, 854719DOI, 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 – 248
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Charakterisierung von Patienten mit atypischem hämolytisch-urämischen Syndrom (aHUS) in Deutschland : Daten aus dem globalen aHUS-RegisterIn: Der Nephrologe, 2019DOI (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. 505DOI (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 – 1075DOI (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. 6003DOI (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. 278DOI (Open Access)
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Dysurische Beschwerden bei einem syrischen JungenIn: Monatsschrift Kinderheilkunde, Jg. 165, 2017, Nr. 6, S. 462 – 464
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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. 14554DOI (Open Access)
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Hämolytisch-urämisches Syndrom im Kindes- und JugendalterIn: Monatsschrift Kinderheilkunde, Jg. 165, 2017, Nr. 11, S. 1005 – 1018
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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 – 1643DOI (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. 98
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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 – 1034DOI, 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 – 1538DOI (Open Access)
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Comparison of different normalization strategies for the analysis of glomerular microRNAs in IgA nephropathyIn: Scientific Reports, Jg. 6, 2016, S. 31992DOI (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 – 865
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Pharmacological treatment of atypical hemolytic-uremic syndromeIn: Expert Opinion on Orphan Drugs, Jg. 2, 2014, Nr. 2, S. 123 – 135
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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 – 887DOI, 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 – 1925
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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 – 415
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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 – 464
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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 – 1248
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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 – 184
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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 – 1298
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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 – 759DOI (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 – 220
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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 – 785
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The diagnostic value of ultrasound in cystic kidney diseasesIn: Pediatric Nephrology, Jg. 25, 2010, Nr. 2, S. 231 – 240DOI (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 – 1166
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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. 1567
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Unusual Manifestation of Posttransplant Lymphoproliferative Disorder in the EsophagusIn: Transplantation Proceedings, Jg. 38, 2006, Nr. 3, S. 693 – 696
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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 – 68
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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 – 59
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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 – 689
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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 – 1211
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Basiliximab in paediatric liver-transplant recipients [Kommentar)In: The Lancet, Jg. 357, 2001, Nr. 9253, S. 388 – 389
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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. Hoboken: Wiley, Jg. 19, 2015, Nr. Suppl. 1, Special Issue: IPTA 8th Congress on Pediatric Transplantation, S. 96
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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. Philadelphia: Lippincott Williams & Wilkins, Jg. 94, 2012, Nr. 10S, S. 260
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Kidneys from Pediatrics Donors <= 5 Year of Age are best used in Paediatric RecipientsIn: Transplant International. Lausanne: Frontiers Media, Jg. 24, 2011, Nr. Suppl. 3, S. 10 – 11
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Steroid-Resistant Nephrotic SyndromeIn: Comprehensive Pediatric Nephrology / Geary, Denis F. (Hrsg.). Philadelphia, PA: Elsevier, 2008, S. 257 – 267
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Exercise-induced acute renal failure due to carnitine palmitoyltransferase II deficiency
Pediatric Nephrology Spring Meeting 2009, March 28 – 31, 2009, Amsterdam, The Netherlands,In: Pediatric Nephrology. Berlin: Springer, Jg. 24, 2009, Nr. 4, S. 918 – 919