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J Senderek

Showing results (1-10 of 25) with videos related to

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Folia Neuropathologica|October 21, 2016
Warburg micro syndrome type 1 associated with peripheral neuropathy and cardiomyopathyD Kabzińska, H Mierzewska, J Senderek, et al.
Molecular Syndromology|January 8, 2013
Molecular genetics of charcot-marie-tooth disease: from genes to genomesH Azzedine, J Senderek, C Rivolta, et al.
Brain Research. Molecular Brain Research|April 11, 2001
A point mutation in the human connexin32 promoter P2 does not correlate with X-linked dominant Charcot-Marie-Tooth neuropathy in GermanyC Bergmann, J M Schröder, S Rudnik-Schöneborn, et al.
Biochemical and Biophysical Research Communications|July 18, 2009
Proteasomal inhibition alters the trafficking of the neurotrophin receptor TrkAT Moises, S Wüller, S Saxena, et al.
Acta Neuropathologica|May 26, 1998
X-linked dominant Charcot-Marie-Tooth disease: nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln)J Senderek, C Bergmann, S Quasthoff, et al.
European Journal of Neurology|April 18, 2007
Mitofusin 2 gene mutation (R94Q) causing severe early-onset axonal polyneuropathy (CMT2A)C Neusch, J Senderek, T Eggermann, et al.
Muscle & Nerve|May 8, 2000
Becker muscular dystrophy combined with X-linked Charcot-Marie-Tooth neuropathyC Bergmann, J Senderek, B Hermanns, et al.
Journal of the Neurological Sciences|November 10, 2001
Phenotypic variation of a novel nonsense mutation in the P0 intracellular domainJ Senderek, V T Ramaekers, K Zerres, et al.
Neuroradiology|November 13, 2002
Hypertrophic nerve roots in a case of Roussy-Lévy syndromeC Haubrich, T Krings, J Senderek, et al.
Journal of Medical Genetics|October 4, 2005
Multi-exon deletions of the PKHD1 gene cause autosomal recessive polycystic kidney disease (ARPKD)C Bergmann, F Küpper, C P Schmitt, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Folia Neuropathologica|October 21, 2016
Warburg micro syndrome type 1 associated with peripheral neuropathy and cardiomyopathyD Kabzińska, H Mierzewska, J Senderek, et al.
Molecular Syndromology|January 8, 2013
Molecular genetics of charcot-marie-tooth disease: from genes to genomesH Azzedine, J Senderek, C Rivolta, et al.
Brain Research. Molecular Brain Research|April 11, 2001
A point mutation in the human connexin32 promoter P2 does not correlate with X-linked dominant Charcot-Marie-Tooth neuropathy in GermanyC Bergmann, J M Schröder, S Rudnik-Schöneborn, et al.
Biochemical and Biophysical Research Communications|July 18, 2009
Proteasomal inhibition alters the trafficking of the neurotrophin receptor TrkAT Moises, S Wüller, S Saxena, et al.
Acta Neuropathologica|May 26, 1998
X-linked dominant Charcot-Marie-Tooth disease: nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln)J Senderek, C Bergmann, S Quasthoff, et al.
European Journal of Neurology|April 18, 2007
Mitofusin 2 gene mutation (R94Q) causing severe early-onset axonal polyneuropathy (CMT2A)C Neusch, J Senderek, T Eggermann, et al.
Muscle & Nerve|May 8, 2000
Becker muscular dystrophy combined with X-linked Charcot-Marie-Tooth neuropathyC Bergmann, J Senderek, B Hermanns, et al.
Journal of the Neurological Sciences|November 10, 2001
Phenotypic variation of a novel nonsense mutation in the P0 intracellular domainJ Senderek, V T Ramaekers, K Zerres, et al.
Neuroradiology|November 13, 2002
Hypertrophic nerve roots in a case of Roussy-Lévy syndromeC Haubrich, T Krings, J Senderek, et al.
Journal of Medical Genetics|October 4, 2005
Multi-exon deletions of the PKHD1 gene cause autosomal recessive polycystic kidney disease (ARPKD)C Bergmann, F Küpper, C P Schmitt, et al.
Pageof 3