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Jan Halbritter

Showing results (11-20 of 117) with videos related to

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Journal of General Internal Medicine|April 19, 2008
Isolated renal relapse of sarcoidosis under low-dose glucocorticoid therapyChristof Mayer, Angela Müller, Jan Halbritter, et al.
BMC Nephrology|September 4, 2019
Retrospective genetic analysis illustrates the spectrum of autosomal Alport syndrome in a case of living-related donor kidney transplantationFriederike Petzold, Anette Bachmann, Carsten Bergmann, et al.
Kidney International|September 24, 2019
The Case | Atypical cysts in a patient with autosomal dominant polycystic kidney diseaseHenning Trawinski, Thomas Karlas, Daniel Seehofer, et al.
Clinical and Experimental Rheumatology|April 18, 2020
ANCA-positive IgA nephropathy in a patient with ANA-positive long-standing rheumatoid arthritis and type 1 diabetesMarco Krasselt, Jan Halbritter, Kerstin Amann, et al.
Frontiers in Pediatrics|March 23, 2018
Update on Hereditary Kidney Stone Disease and Introduction of a New Clinical Patient Registry in GermanyJan Halbritter, Anna Seidel, Luise Müller, et al.
BMC Medical Genetics|October 14, 2016
Diagnosing FSGS without kidney biopsy - a novel INF2-mutation in a family with ESRD of unknown originJohannes Münch, Maik Grohmann, Tom H Lindner, et al.
Clinical Kidney Journal|June 27, 2022
Novel somatic <i>PBX1</i> mosaicism likely masking syndromic CAKUT in an adult with bilateral kidney hypoplasiaFriederike Petzold, Wenjun Jin, Elena Hantmann, et al.
Frontiers in Genetics|June 4, 2019
Deleterious Impact of a Novel <i>CFH</i> Splice Site Variant in Atypical Hemolytic Uremic SyndromeRia Schönauer, Anna Seidel, Maik Grohmann, et al.
Frontiers in Genetics|July 12, 2021
Challenging Disease Ontology by Instances of Atypical <i>PKHD1</i> and <i>PKD1</i> GeneticsJonathan de Fallois, Ria Schönauer, Johannes Münch, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 23, 2021
Emicizumab treatment in chronic intermittent haemodialysisMaria Weise, Annelie Siegemund, Lydia Böhme, et al.
Pageof 12

Showing results (11-20 of 117) with videos related to

Sort By:
Pageof 12
Journal of General Internal Medicine|April 19, 2008
Isolated renal relapse of sarcoidosis under low-dose glucocorticoid therapyChristof Mayer, Angela Müller, Jan Halbritter, et al.
BMC Nephrology|September 4, 2019
Retrospective genetic analysis illustrates the spectrum of autosomal Alport syndrome in a case of living-related donor kidney transplantationFriederike Petzold, Anette Bachmann, Carsten Bergmann, et al.
Kidney International|September 24, 2019
The Case | Atypical cysts in a patient with autosomal dominant polycystic kidney diseaseHenning Trawinski, Thomas Karlas, Daniel Seehofer, et al.
Clinical and Experimental Rheumatology|April 18, 2020
ANCA-positive IgA nephropathy in a patient with ANA-positive long-standing rheumatoid arthritis and type 1 diabetesMarco Krasselt, Jan Halbritter, Kerstin Amann, et al.
Frontiers in Pediatrics|March 23, 2018
Update on Hereditary Kidney Stone Disease and Introduction of a New Clinical Patient Registry in GermanyJan Halbritter, Anna Seidel, Luise Müller, et al.
BMC Medical Genetics|October 14, 2016
Diagnosing FSGS without kidney biopsy - a novel INF2-mutation in a family with ESRD of unknown originJohannes Münch, Maik Grohmann, Tom H Lindner, et al.
Clinical Kidney Journal|June 27, 2022
Novel somatic <i>PBX1</i> mosaicism likely masking syndromic CAKUT in an adult with bilateral kidney hypoplasiaFriederike Petzold, Wenjun Jin, Elena Hantmann, et al.
Frontiers in Genetics|June 4, 2019
Deleterious Impact of a Novel <i>CFH</i> Splice Site Variant in Atypical Hemolytic Uremic SyndromeRia Schönauer, Anna Seidel, Maik Grohmann, et al.
Frontiers in Genetics|July 12, 2021
Challenging Disease Ontology by Instances of Atypical <i>PKHD1</i> and <i>PKD1</i> GeneticsJonathan de Fallois, Ria Schönauer, Johannes Münch, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 23, 2021
Emicizumab treatment in chronic intermittent haemodialysisMaria Weise, Annelie Siegemund, Lydia Böhme, et al.
Pageof 12