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Carsten Bergmann

Showing results (61-70 of 228) with videos related to

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Pediatric Nephrology (Berlin, Germany)|March 11, 2015
A complicated case of atypical hemolytic uremic syndrome with frequent relapses under eculizumabGesa Schalk, Michael Kirschfink, Cyrill Wehling, et al.
Gene Expression Patterns : GEP|June 6, 2006
Cloning, expression and characterization of the murine orthologue of SBF2, the gene mutated in Charcot-Marie-Tooth disease type 4B2Jutta Kirfel, Jan Senderek, Markus Moser, et al.
American Journal of Medical Genetics. Part A|December 23, 2017
Expanding the phenotype associated with biallelic WDR60 mutations: Siblings with retinal degeneration and polydactyly lacking other features of short rib thoracic dystrophiesNaseebullah Kakar, Denise Horn, Eva Decker, et al.
Gut|September 28, 2014
Somatic loss of polycystic disease genes contributes to the formation of isolated and polycystic liver cystsManoe J Janssen, Jody Salomon, Wybrich R Cnossen, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
Tectonic gene mutations in patients with Joubert syndromePeter Huppke, Eike Wegener, Helena Böhrer-Rabel, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 13, 2012
COL4A5-associated X-linked Alport syndrome in a female patient with early inner ear deafness due to a mutation in MYH9Katja Strasser, Julia Hoefele, Carsten Bergmann, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 19, 2016
Systemic complement activation and complement gene analysis in enterohaemorrhagic Escherichia coli-associated paediatric haemolytic uraemic syndromeThurid Ahlenstiel-Grunow, Svenja Hachmeister, Franz Christoph Bange, et al.
Pediatric Blood & Cancer|September 22, 2016
Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith-Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesisNadine Bachmann, Roman Crazzolara, Florian Bohne, et al.
Pediatrics|November 29, 2023
CD55 Deficiency With Budd-Chiari Syndrome Treated by Liver Transplantation and EculizumabSinja Ohlsson, Elke Lainka, Christoph Hünseler, et al.
Clinical Kidney Journal|December 12, 2017
Effective immunosuppressive management with belatacept and eculizumab in post-transplant aHUS due to a homozygous deletion of <i>CFHR1</i>/<i>CFHR3</i> and the presence of CFH antibodiesJohannes Münch, Anette Bachmann, Maik Grohmann, et al.
Pageof 23

Showing results (61-70 of 228) with videos related to

Sort By:
Pageof 23
Pediatric Nephrology (Berlin, Germany)|March 11, 2015
A complicated case of atypical hemolytic uremic syndrome with frequent relapses under eculizumabGesa Schalk, Michael Kirschfink, Cyrill Wehling, et al.
Gene Expression Patterns : GEP|June 6, 2006
Cloning, expression and characterization of the murine orthologue of SBF2, the gene mutated in Charcot-Marie-Tooth disease type 4B2Jutta Kirfel, Jan Senderek, Markus Moser, et al.
American Journal of Medical Genetics. Part A|December 23, 2017
Expanding the phenotype associated with biallelic WDR60 mutations: Siblings with retinal degeneration and polydactyly lacking other features of short rib thoracic dystrophiesNaseebullah Kakar, Denise Horn, Eva Decker, et al.
Gut|September 28, 2014
Somatic loss of polycystic disease genes contributes to the formation of isolated and polycystic liver cystsManoe J Janssen, Jody Salomon, Wybrich R Cnossen, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
Tectonic gene mutations in patients with Joubert syndromePeter Huppke, Eike Wegener, Helena Böhrer-Rabel, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 13, 2012
COL4A5-associated X-linked Alport syndrome in a female patient with early inner ear deafness due to a mutation in MYH9Katja Strasser, Julia Hoefele, Carsten Bergmann, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 19, 2016
Systemic complement activation and complement gene analysis in enterohaemorrhagic Escherichia coli-associated paediatric haemolytic uraemic syndromeThurid Ahlenstiel-Grunow, Svenja Hachmeister, Franz Christoph Bange, et al.
Pediatric Blood & Cancer|September 22, 2016
Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith-Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesisNadine Bachmann, Roman Crazzolara, Florian Bohne, et al.
Pediatrics|November 29, 2023
CD55 Deficiency With Budd-Chiari Syndrome Treated by Liver Transplantation and EculizumabSinja Ohlsson, Elke Lainka, Christoph Hünseler, et al.
Clinical Kidney Journal|December 12, 2017
Effective immunosuppressive management with belatacept and eculizumab in post-transplant aHUS due to a homozygous deletion of <i>CFHR1</i>/<i>CFHR3</i> and the presence of CFH antibodiesJohannes Münch, Anette Bachmann, Maik Grohmann, et al.
Pageof 23