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M Vorgerd

Showing results (51-60 of 65) with videos related to

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Neurology|December 13, 2000
Oxidative stress in patients with Friedreich ataxiaJ B Schulz, T Dehmer, L Schöls, et al.
Stem Cell Research|February 3, 2024
Generation of two hiPSCs lines of two patients carrying truncating mutations in the dimerization domain of filamin CN M Daya, K Döring, H Zhuge, et al.
Archives of Neurology|July 13, 2000
Creatine therapy in myophosphorylase deficiency (McArdle disease): a placebo-controlled crossover trialM Vorgerd, T Grehl, M Jager, et al.
Archives of Neurology|October 6, 1997
Spinocerebellar ataxia type 2. Genotype and phenotype in German kindredsL Schöls, S Gispert, M Vorgerd, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|October 14, 2004
L-carnitine and creatine in Friedreich's ataxia. A randomized, placebo-controlled crossover trialL Schöls, J Zange, M Abele, et al.
Diabetes|May 20, 1998
An association between NIDDM and a GAA trinucleotide repeat polymorphism in the X25/frataxin (Friedreich's ataxia) geneM Ristow, E Giannakidou, J Hebinck, et al.
Brain : a Journal of Neurology|April 19, 2007
Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350PM C Walter, P Reilich, A Huebner, et al.
Stem Cell Research|October 15, 2023
Generation of two human iPSC lines (HIMRi002-A and HIMRi003-A) derived from Caveolinopathy patients with rippling muscle diseaseA Boeing, L Mavrommatis, N M Daya, et al.
Nature Genetics|June 30, 2001
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle diseaseR C Betz, B G Schoser, D Kasper, et al.
Neuromuscular Disorders : NMD|December 28, 2005
Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosisM von der Hagen, J Schallner, A M Kaindl, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Neurology|December 13, 2000
Oxidative stress in patients with Friedreich ataxiaJ B Schulz, T Dehmer, L Schöls, et al.
Stem Cell Research|February 3, 2024
Generation of two hiPSCs lines of two patients carrying truncating mutations in the dimerization domain of filamin CN M Daya, K Döring, H Zhuge, et al.
Archives of Neurology|July 13, 2000
Creatine therapy in myophosphorylase deficiency (McArdle disease): a placebo-controlled crossover trialM Vorgerd, T Grehl, M Jager, et al.
Archives of Neurology|October 6, 1997
Spinocerebellar ataxia type 2. Genotype and phenotype in German kindredsL Schöls, S Gispert, M Vorgerd, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|October 14, 2004
L-carnitine and creatine in Friedreich's ataxia. A randomized, placebo-controlled crossover trialL Schöls, J Zange, M Abele, et al.
Diabetes|May 20, 1998
An association between NIDDM and a GAA trinucleotide repeat polymorphism in the X25/frataxin (Friedreich's ataxia) geneM Ristow, E Giannakidou, J Hebinck, et al.
Brain : a Journal of Neurology|April 19, 2007
Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350PM C Walter, P Reilich, A Huebner, et al.
Stem Cell Research|October 15, 2023
Generation of two human iPSC lines (HIMRi002-A and HIMRi003-A) derived from Caveolinopathy patients with rippling muscle diseaseA Boeing, L Mavrommatis, N M Daya, et al.
Nature Genetics|June 30, 2001
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle diseaseR C Betz, B G Schoser, D Kasper, et al.
Neuromuscular Disorders : NMD|December 28, 2005
Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosisM von der Hagen, J Schallner, A M Kaindl, et al.
Pageof 7