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W Mortier

Showing results (51-60 of 61) with videos related to

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Fortschritte Der Ophthalmologie : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 1, 1983
[Clinical, morphological and biochemical findings in the Kearns-Sayre syndrome]W Hammerstein, W Mortier, E A Noack, 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.
Pathology, Research and Practice|November 1, 1988
Mitochondrial myopathies with necrotizing encephalopathy of the Leigh typeJ Peiffer, B Kustermann-Kuhn, W Mortier, et al.
Annals of Neurology|March 20, 1998
Mutation analysis in myophosphorylase deficiency (McArdle's disease)M Vorgerd, C Kubisch, B Burwinkel, et al.
Neuromuscular Disorders : NMD|July 16, 2002
A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian populationM Gross, E Rötzer, P Kölle, 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.
Anasthesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS|June 9, 1998
[Regional distribution of predisposition to maligant hyperthermia in Germany: tate in 1997]E Hartung, M Anetseder, D Olthoff, et al.
Neurology|June 11, 2003
Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patientsJ S Müller, G Mildner, W Müller-Felber, et al.
Neurology|October 26, 1999
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic originA Abicht, R Stucka, V Karcagi, 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.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Fortschritte Der Ophthalmologie : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 1, 1983
[Clinical, morphological and biochemical findings in the Kearns-Sayre syndrome]W Hammerstein, W Mortier, E A Noack, 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.
Pathology, Research and Practice|November 1, 1988
Mitochondrial myopathies with necrotizing encephalopathy of the Leigh typeJ Peiffer, B Kustermann-Kuhn, W Mortier, et al.
Annals of Neurology|March 20, 1998
Mutation analysis in myophosphorylase deficiency (McArdle's disease)M Vorgerd, C Kubisch, B Burwinkel, et al.
Neuromuscular Disorders : NMD|July 16, 2002
A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian populationM Gross, E Rötzer, P Kölle, 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.
Anasthesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS|June 9, 1998
[Regional distribution of predisposition to maligant hyperthermia in Germany: tate in 1997]E Hartung, M Anetseder, D Olthoff, et al.
Neurology|June 11, 2003
Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patientsJ S Müller, G Mildner, W Müller-Felber, et al.
Neurology|October 26, 1999
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic originA Abicht, R Stucka, V Karcagi, 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.
Pageof 7