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Mato Nagel

Showing results (1-10 of 28) with videos related to

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Deutsches Arzteblatt International|June 16, 2026
Paradigm ShiftMato Nagel
Human Mutation|June 15, 2005
Novel COL4A5, COL4A4, and COL4A3 mutations in Alport syndromeMato Nagel, Sylvia Nagorka, Oliver Gross
SAGE Open Medical Case Reports|August 25, 2017
Epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome in a European child with <i>KCNJ10</i> mutations: A case reportAntigone Papavasiliou, Katerina Foska, John Ioannou, et al.
Hormone Research in Paediatrics|May 11, 2010
Pseudohypoaldosteronism type 1 due to a novel mutation in the mineralocorticoid receptor geneLindsey A Loomba-Albrecht, Mato Nagel, Andrew A Bremer
Wiener Klinische Wochenschrift|January 27, 2016
Autosomal dominant tubulointerstitial kidney disease caused by uromodulin mutations: seek and you will findGabriele Raffler, Emanuel Zitt, Hannelore Sprenger-Mähr, et al.
BMC Nephrology|January 12, 2005
Polymorphisms of the insertion / deletion ACE and M235T AGT genes and hypertension: surprising new findings and meta-analysis of dataAdrian Mondry, Marie Loh, Pengbo Liu, et al.
The New England Journal of Medicine|October 25, 2013
Deficiency in complement factor BCharlotte Slade, Julian Bosco, Gary Unglik, et al.
Case Reports in Pediatrics|May 22, 2013
Erratum to "endolymphatic sac enlargement in a girl with a novel mutation for distal renal tubular acidosis and severe deafness"Nikki Rink, Martin Bitzan, Gus O'Gorman, 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.
World Journal of Pediatrics : WJP|June 3, 2011
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis in three siblings having the same genetic lesion but different clinical presentationsHilary H Seeley, Lindsey A Loomba-Albrecht, Mato Nagel, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Deutsches Arzteblatt International|June 16, 2026
Paradigm ShiftMato Nagel
Human Mutation|June 15, 2005
Novel COL4A5, COL4A4, and COL4A3 mutations in Alport syndromeMato Nagel, Sylvia Nagorka, Oliver Gross
SAGE Open Medical Case Reports|August 25, 2017
Epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome in a European child with <i>KCNJ10</i> mutations: A case reportAntigone Papavasiliou, Katerina Foska, John Ioannou, et al.
Hormone Research in Paediatrics|May 11, 2010
Pseudohypoaldosteronism type 1 due to a novel mutation in the mineralocorticoid receptor geneLindsey A Loomba-Albrecht, Mato Nagel, Andrew A Bremer
Wiener Klinische Wochenschrift|January 27, 2016
Autosomal dominant tubulointerstitial kidney disease caused by uromodulin mutations: seek and you will findGabriele Raffler, Emanuel Zitt, Hannelore Sprenger-Mähr, et al.
BMC Nephrology|January 12, 2005
Polymorphisms of the insertion / deletion ACE and M235T AGT genes and hypertension: surprising new findings and meta-analysis of dataAdrian Mondry, Marie Loh, Pengbo Liu, et al.
The New England Journal of Medicine|October 25, 2013
Deficiency in complement factor BCharlotte Slade, Julian Bosco, Gary Unglik, et al.
Case Reports in Pediatrics|May 22, 2013
Erratum to "endolymphatic sac enlargement in a girl with a novel mutation for distal renal tubular acidosis and severe deafness"Nikki Rink, Martin Bitzan, Gus O'Gorman, 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.
World Journal of Pediatrics : WJP|June 3, 2011
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis in three siblings having the same genetic lesion but different clinical presentationsHilary H Seeley, Lindsey A Loomba-Albrecht, Mato Nagel, et al.
Pageof 3