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Carsten Bergmann

Showing results (21-30 of 228) with videos related to

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Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|April 5, 2014
Results of fibrillin-1 gene analysis in children from inbred families with lens subluxationArif O Khan, Hanno J Bolz, Carsten Bergmann
Journal of Hepatology|March 13, 2012
Dosage-sensitive network in polycystic kidney and liver disease: multiple mutations cause severe hepatic and neurological complicationsJens Kleffmann, Valeska Frank, Andreas Ferbert, et al.
Best Practice & Research. Clinical Gastroenterology|October 20, 2010
Congenital fibrocystic liver diseasesJoost P H Drenth, Melissa Chrispijn, Carsten Bergmann
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|April 5, 2014
Early-onset severe retinal dystrophy as the initial presentation of IFT140-related skeletal ciliopathyArif O Khan, Hanno J Bolz, Carsten Bergmann
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 19, 2025
Evinacumab as an adjunct to lipid apheresis in an infant with homozygous familial hypercholesterolemiaChristian Stirnkorb, Verena Ney, Carsten Bergmann, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|September 21, 2013
First cases of dominant optic atrophy in Saudi Arabia: report of two novel OPA1 mutationsAlberto Galvez-Ruiz, Christine Neuhaus, Carsten Bergmann, et al.
The British Journal of Ophthalmology|October 25, 2014
A TULP1 founder mutation, p.Gln301*, underlies a recognisable congenital rod-cone dystrophy phenotype on the Arabian PeninsulaArif O Khan, Carsten Bergmann, Tobias Eisenberger, et al.
Clinical Nephrology|September 25, 2014
Neonatal ascites in autosomal recessive polycystic kidney disease (ARPKD)Galina Ling, Daniel Landau, Carsten Bergmann, et al.
Scientific Reports|November 6, 2023
Kif21a deficiency leads to impaired glomerular filtration barrier functionHanna Riedmann, Séverine Kayser, Martin Helmstädter, et al.
Cerebrovascular Diseases (Basel, Switzerland)|July 18, 2013
Ruptured cerebral aneurysm and acute bilateral carotid artery dissection in a patient with polycystic kidney disease and polycystic liver diseaseChristian Roth, Jens Kleffmann, Carsten Bergmann, et al.
Pageof 23

Showing results (21-30 of 228) with videos related to

Sort By:
Pageof 23
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|April 5, 2014
Results of fibrillin-1 gene analysis in children from inbred families with lens subluxationArif O Khan, Hanno J Bolz, Carsten Bergmann
Journal of Hepatology|March 13, 2012
Dosage-sensitive network in polycystic kidney and liver disease: multiple mutations cause severe hepatic and neurological complicationsJens Kleffmann, Valeska Frank, Andreas Ferbert, et al.
Best Practice & Research. Clinical Gastroenterology|October 20, 2010
Congenital fibrocystic liver diseasesJoost P H Drenth, Melissa Chrispijn, Carsten Bergmann
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|April 5, 2014
Early-onset severe retinal dystrophy as the initial presentation of IFT140-related skeletal ciliopathyArif O Khan, Hanno J Bolz, Carsten Bergmann
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 19, 2025
Evinacumab as an adjunct to lipid apheresis in an infant with homozygous familial hypercholesterolemiaChristian Stirnkorb, Verena Ney, Carsten Bergmann, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|September 21, 2013
First cases of dominant optic atrophy in Saudi Arabia: report of two novel OPA1 mutationsAlberto Galvez-Ruiz, Christine Neuhaus, Carsten Bergmann, et al.
The British Journal of Ophthalmology|October 25, 2014
A TULP1 founder mutation, p.Gln301*, underlies a recognisable congenital rod-cone dystrophy phenotype on the Arabian PeninsulaArif O Khan, Carsten Bergmann, Tobias Eisenberger, et al.
Clinical Nephrology|September 25, 2014
Neonatal ascites in autosomal recessive polycystic kidney disease (ARPKD)Galina Ling, Daniel Landau, Carsten Bergmann, et al.
Scientific Reports|November 6, 2023
Kif21a deficiency leads to impaired glomerular filtration barrier functionHanna Riedmann, Séverine Kayser, Martin Helmstädter, et al.
Cerebrovascular Diseases (Basel, Switzerland)|July 18, 2013
Ruptured cerebral aneurysm and acute bilateral carotid artery dissection in a patient with polycystic kidney disease and polycystic liver diseaseChristian Roth, Jens Kleffmann, Carsten Bergmann, et al.
Pageof 23