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M Vorgerd

Showing results (41-50 of 65) with videos related to

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Annals of Neurology|April 13, 2000
Novel missense mutations in the glycogen-branching enzyme gene in adult polyglucosan body diseaseF Ziemssen, E Sindern, J M Schröder, et al.
Neurology|January 5, 2002
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutationM Vorgerd, K Ricker, F Ziemssen, et al.
Stem Cell Research|September 25, 2023
Generation of a human iPSC line (HIMRi001-A) from a patient with filaminopathyN M Daya, L Mavrommatis, H Zhuge, et al.
Der Nervenarzt|November 23, 2013
[Diagnosis and therapy of late onset Pompe disease]A Schüller, C Kornblum, M Deschauer, et al.
Journal of Neurology|April 4, 2007
Analysis of spectrum and frequencies of mutations in McArdle disease. Identification of 13 novel mutationsM Deschauer, A Morgenroth, P R Joshi, et al.
Stem Cell Research|June 19, 2024
Generation of two induced pluripotent stem cell lines (HIMRi006-A and HIMRi007-A) from Pompe patients with infantile and late disease onsetL Volke, N M Daya, K Döring, et al.
Neurology|July 23, 2003
Adult polyglucosan body disease: a postmortem correlation studyE Sindern, F Ziemssen, T Ziemssen, et al.
Annals of Neurology|March 20, 1998
Mutation analysis in myophosphorylase deficiency (McArdle's disease)M Vorgerd, C Kubisch, B Burwinkel, et al.
European Radiology|December 19, 2018
Muscle diffusion tensor imaging in glycogen storage disease V (McArdle disease)R Rehmann, L Schlaffke, M Froeling, et al.
Neurology|January 26, 2005
Immune-mediated rippling muscle diseaseW J Schulte-Mattler, R A Kley, E Rothenfusser-Korber, et al.
Pageof 7

Showing results (41-50 of 65) with videos related to

Sort By:
Pageof 7
Annals of Neurology|April 13, 2000
Novel missense mutations in the glycogen-branching enzyme gene in adult polyglucosan body diseaseF Ziemssen, E Sindern, J M Schröder, et al.
Neurology|January 5, 2002
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutationM Vorgerd, K Ricker, F Ziemssen, et al.
Stem Cell Research|September 25, 2023
Generation of a human iPSC line (HIMRi001-A) from a patient with filaminopathyN M Daya, L Mavrommatis, H Zhuge, et al.
Der Nervenarzt|November 23, 2013
[Diagnosis and therapy of late onset Pompe disease]A Schüller, C Kornblum, M Deschauer, et al.
Journal of Neurology|April 4, 2007
Analysis of spectrum and frequencies of mutations in McArdle disease. Identification of 13 novel mutationsM Deschauer, A Morgenroth, P R Joshi, et al.
Stem Cell Research|June 19, 2024
Generation of two induced pluripotent stem cell lines (HIMRi006-A and HIMRi007-A) from Pompe patients with infantile and late disease onsetL Volke, N M Daya, K Döring, et al.
Neurology|July 23, 2003
Adult polyglucosan body disease: a postmortem correlation studyE Sindern, F Ziemssen, T Ziemssen, et al.
Annals of Neurology|March 20, 1998
Mutation analysis in myophosphorylase deficiency (McArdle's disease)M Vorgerd, C Kubisch, B Burwinkel, et al.
European Radiology|December 19, 2018
Muscle diffusion tensor imaging in glycogen storage disease V (McArdle disease)R Rehmann, L Schlaffke, M Froeling, et al.
Neurology|January 26, 2005
Immune-mediated rippling muscle diseaseW J Schulte-Mattler, R A Kley, E Rothenfusser-Korber, et al.
Pageof 7