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Corinna Berghoff

Showing results (1-10 of 7) with videos related to

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Muscle & Nerve|June 29, 2004
Annexin expression in inflammatory myopathiesStefan Probst-Cousin, Corinna Berghoff, Bernhard Neundörfer, et al.
Revista De Biologia Tropical|February 28, 2015
A Costa Rican family affected with Charcot-Marie-Tooth disease due to the myelin protein zero (MPZ) p.Thr124Met mutation shares the Belgian haplotypeAlejandro Leal, Corinna Berghoff, Martin Berghoff, et al.
Neurological Research|October 2, 2008
Late onset autosomal dominant Charcot-Marie-Tooth 2 neuropathy in a Costa Rican familyCorinna Berghoff, Martin Berghoff, Alejandro Leal, et al.
Neuromuscular Disorders : NMD|April 22, 2004
Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3Corinna Berghoff, Martin Berghoff, Alejandro Leal, et al.
Neurogenetics|July 25, 2018
The polynucleotide kinase 3'-phosphatase gene (PNKP) is involved in Charcot-Marie-Tooth disease (CMT2B2) previously related to MED25Alejandro Leal, Sixto Bogantes-Ledezma, Arif B Ekici, et al.
Neurogenetics|July 8, 2003
Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one familyAlejandro Leal, Corinna Berghoff, Martin Berghoff, 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.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Muscle & Nerve|June 29, 2004
Annexin expression in inflammatory myopathiesStefan Probst-Cousin, Corinna Berghoff, Bernhard Neundörfer, et al.
Revista De Biologia Tropical|February 28, 2015
A Costa Rican family affected with Charcot-Marie-Tooth disease due to the myelin protein zero (MPZ) p.Thr124Met mutation shares the Belgian haplotypeAlejandro Leal, Corinna Berghoff, Martin Berghoff, et al.
Neurological Research|October 2, 2008
Late onset autosomal dominant Charcot-Marie-Tooth 2 neuropathy in a Costa Rican familyCorinna Berghoff, Martin Berghoff, Alejandro Leal, et al.
Neuromuscular Disorders : NMD|April 22, 2004
Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3Corinna Berghoff, Martin Berghoff, Alejandro Leal, et al.
Neurogenetics|July 25, 2018
The polynucleotide kinase 3'-phosphatase gene (PNKP) is involved in Charcot-Marie-Tooth disease (CMT2B2) previously related to MED25Alejandro Leal, Sixto Bogantes-Ledezma, Arif B Ekici, et al.
Neurogenetics|July 8, 2003
Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one familyAlejandro Leal, Corinna Berghoff, Martin Berghoff, 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.
Pageof 1