Kathrin Huehne - JoVE Visualize

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Neuroscience Letters|January 29, 2010

Lack of genetic association of neutral endopeptidase (NEP) with complex regional pain syndrome (CRPS)Kathrin Huehne, Ute Schaal, Stefan Leis, et al.

Neuromuscular Disorders : NMD|December 14, 2007

Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosisKathrin Huehne, Christiane Zweier, Klaus Raab, et al.

Brain : a Journal of Neurology|May 19, 2010

Alternative splicing may contribute to time-dependent manifestation of inherited erythromelalgiaJin-Sung Choi, Xiaoyang Cheng, Edmund Foster, et al.

Neurogenetics|March 18, 2009

Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal modelsAlejandro Leal, Kathrin Huehne, Finn Bauer, et al.

American Journal of Human Genetics|October 24, 2003

Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathyJan Senderek, Carsten Bergmann, Claudia Stendel, et al.

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Showing results (11-20 of 15) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 15 results.

Neuroscience Letters|January 29, 2010

Lack of genetic association of neutral endopeptidase (NEP) with complex regional pain syndrome (CRPS)Kathrin Huehne, Ute Schaal, Stefan Leis, et al.

Neuromuscular Disorders : NMD|December 14, 2007

Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosisKathrin Huehne, Christiane Zweier, Klaus Raab, et al.

Brain : a Journal of Neurology|May 19, 2010

Alternative splicing may contribute to time-dependent manifestation of inherited erythromelalgiaJin-Sung Choi, Xiaoyang Cheng, Edmund Foster, et al.

Neurogenetics|March 18, 2009

Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal modelsAlejandro Leal, Kathrin Huehne, Finn Bauer, et al.

American Journal of Human Genetics|October 24, 2003

Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathyJan Senderek, Carsten Bergmann, Claudia Stendel, et al.

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