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Jan Senderek

Showing results (1-10 of 104) with videos related to

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European Journal of Neurology|January 25, 2021
PLEKHG5: Merging phenotypes and disease mechanisms in Charcot-Marie-Tooth neuropathy and lower motor neuron diseaseJan Senderek
Fortschritte Der Neurologie-Psychiatrie|September 25, 2018
[Immune-mediated / inflammatory and hereditary neuropathies - overview and diagnostic algorithm]Beate Schlotter-Weigel, Jan Senderek
Neuropediatrics|June 10, 2017
Hereditary Neuropathies: Update 2017Sabine Rudnik-Schöneborn, Michaela Auer-Grumbach, Jan Senderek
Journal of Nephrology|July 2, 2003
Autosomal recessive polycystic kidney disease (ARPKD)Klaus Zerres, Sabine Rudnik-Schöneborn, Jan Senderek, et al.
Journal of the Peripheral Nervous System : JPNS|October 11, 2008
Small Rho GTPases are key regulators of peripheral nerve biology in health and diseaseSven Krause, Claudia Stendel, Jan Senderek, et al.
Journal of Human Genetics|August 10, 2006
Functional analysis of PKHD1 splicing in autosomal recessive polycystic kidney diseaseCarsten Bergmann, Valeska Frank, Fabian Küpper, 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.
Journal of Pediatric Neurosciences|January 28, 2015
SIL1-negative Marinesco-Sjögren syndrome: First report of two sibs from IndiaPrashant Jauhari, Jitendra K Sahu, Andreas Roos, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 8, 2005
Light microscopic, immunohistochemical, and ultrastructural findings in congenital fibular aplasia or hypoplasia (FAH)Benita Hermanns-Sachweh, Anne Stemper, Bernd Klosterhalfen, et al.
Pageof 11

Showing results (1-10 of 104) with videos related to

Sort By:
Pageof 11
European Journal of Neurology|January 25, 2021
PLEKHG5: Merging phenotypes and disease mechanisms in Charcot-Marie-Tooth neuropathy and lower motor neuron diseaseJan Senderek
Fortschritte Der Neurologie-Psychiatrie|September 25, 2018
[Immune-mediated / inflammatory and hereditary neuropathies - overview and diagnostic algorithm]Beate Schlotter-Weigel, Jan Senderek
Neuropediatrics|June 10, 2017
Hereditary Neuropathies: Update 2017Sabine Rudnik-Schöneborn, Michaela Auer-Grumbach, Jan Senderek
Journal of Nephrology|July 2, 2003
Autosomal recessive polycystic kidney disease (ARPKD)Klaus Zerres, Sabine Rudnik-Schöneborn, Jan Senderek, et al.
Journal of the Peripheral Nervous System : JPNS|October 11, 2008
Small Rho GTPases are key regulators of peripheral nerve biology in health and diseaseSven Krause, Claudia Stendel, Jan Senderek, et al.
Journal of Human Genetics|August 10, 2006
Functional analysis of PKHD1 splicing in autosomal recessive polycystic kidney diseaseCarsten Bergmann, Valeska Frank, Fabian Küpper, 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.
Journal of Pediatric Neurosciences|January 28, 2015
SIL1-negative Marinesco-Sjögren syndrome: First report of two sibs from IndiaPrashant Jauhari, Jitendra K Sahu, Andreas Roos, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|October 8, 2005
Light microscopic, immunohistochemical, and ultrastructural findings in congenital fibular aplasia or hypoplasia (FAH)Benita Hermanns-Sachweh, Anne Stemper, Bernd Klosterhalfen, et al.
Pageof 11