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Carsten Bergmann

Showing results (31-40 of 228) with videos related to

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Journal of Pediatric Ophthalmology and Strabismus|July 18, 2014
Limited ocular motility in a child with 3q23 microdeletion ("blepharophimosis syndrome plus")Arif O Khan, Sandra Nagl, Carsten Bergmann, 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.
Ophthalmic Genetics|December 6, 2014
A distinct vitreo-retinal dystrophy with early-onset cataract from recessive KCNJ13 mutationsArif O Khan, Carsten Bergmann, Christine Neuhaus, et al.
Pediatric Nephrology (Berlin, Germany)|March 16, 2026
Severe systemic lupus erythematosus with thrombotic microangiopathy: rescue therapy with pegcetacoplanChristian Stirnkorb, Verena Ney, Bhavna Issar, et al.
The New England Journal of Medicine|July 19, 2008
Perinatal deaths in a family with autosomal dominant polycystic kidney disease and a PKD2 mutationCarsten Bergmann, Nadina Ortiz Brüchle, Valeska Frank, et al.
Molecular Vision|January 8, 2020
Long-term follow-up of retinal function and structure in <i>TRPM1</i>-associated complete congenital stationary night blindnessHaneen Al-Hujaili, Ibrahim Taskintuna, Christine Neuhaus, et al.
Journal of Nephrology|July 2, 2003
Autosomal recessive polycystic kidney disease (ARPKD)Klaus Zerres, Sabine Rudnik-Schöneborn, Jan Senderek, 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.
Human Mutation|February 12, 2005
Algorithm for efficient PKHD1 mutation screening in autosomal recessive polycystic kidney disease (ARPKD)Carsten Bergmann, Fabian Küpper, Christian Dornia, et al.
Archives of Neurology|April 23, 2003
Transient, recurrent, white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexin 32 mutationC Oliver Hanemann, Carsten Bergmann, Jan Senderek, et al.
Pageof 23

Showing results (31-40 of 228) with videos related to

Sort By:
Pageof 23
Journal of Pediatric Ophthalmology and Strabismus|July 18, 2014
Limited ocular motility in a child with 3q23 microdeletion ("blepharophimosis syndrome plus")Arif O Khan, Sandra Nagl, Carsten Bergmann, 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.
Ophthalmic Genetics|December 6, 2014
A distinct vitreo-retinal dystrophy with early-onset cataract from recessive KCNJ13 mutationsArif O Khan, Carsten Bergmann, Christine Neuhaus, et al.
Pediatric Nephrology (Berlin, Germany)|March 16, 2026
Severe systemic lupus erythematosus with thrombotic microangiopathy: rescue therapy with pegcetacoplanChristian Stirnkorb, Verena Ney, Bhavna Issar, et al.
The New England Journal of Medicine|July 19, 2008
Perinatal deaths in a family with autosomal dominant polycystic kidney disease and a PKD2 mutationCarsten Bergmann, Nadina Ortiz Brüchle, Valeska Frank, et al.
Molecular Vision|January 8, 2020
Long-term follow-up of retinal function and structure in <i>TRPM1</i>-associated complete congenital stationary night blindnessHaneen Al-Hujaili, Ibrahim Taskintuna, Christine Neuhaus, et al.
Journal of Nephrology|July 2, 2003
Autosomal recessive polycystic kidney disease (ARPKD)Klaus Zerres, Sabine Rudnik-Schöneborn, Jan Senderek, 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.
Human Mutation|February 12, 2005
Algorithm for efficient PKHD1 mutation screening in autosomal recessive polycystic kidney disease (ARPKD)Carsten Bergmann, Fabian Küpper, Christian Dornia, et al.
Archives of Neurology|April 23, 2003
Transient, recurrent, white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexin 32 mutationC Oliver Hanemann, Carsten Bergmann, Jan Senderek, et al.
Pageof 23