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H F Busch

Showing results (51-60 of 63) with videos related to

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Experimental Cell Research|November 1, 1984
Uptake and stability of human and bovine acid alpha-glucosidase in cultured fibroblasts and skeletal muscle cells from glycogenosis type II patientsA J Reuser, M A Kroos, N J Ponne, et al.
Heart (British Cardiac Society)|March 20, 1998
The heart in limb girdle muscular dystrophyA J van der Kooi, W G de Voogt, P G Barth, et al.
International Journal of Rehabilitation Research. Internationale Zeitschrift Fur Rehabilitationsforschung. Revue Internationale De Recherches De Readaptation|October 23, 1997
Vocational perspectives and neuromuscular disordersF Andries, C W Wevers, A R Wintzen, et al.
Annals of Neurology|May 1, 1996
A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvementA J van der Kooi, T M Ledderhof, W G de Voogt, et al.
Clinical Genetics|January 1, 1981
Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency)M C Loonen, A W Schram, J F Koster, et al.
Journal of the Neurological Sciences|May 1, 1995
Differential diagnosis in spinal and bulbar muscular atrophy clinical and molecular aspectsG J Jöbsis, E S Louwerse, M de Visser, et al.
Neurology|October 1, 1981
A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studiesM C Loonen, H F Busch, J F Koster, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotypeH R Scholte, R N Van Coster, P C de Jonge, et al.
Brain : a Journal of Neurology|December 16, 1997
Miyoshi-type distal muscular dystrophy. Clinical spectrum in 24 Dutch patientsW H Linssen, N C Notermans, Y Van der Graaf, et al.
Biochimica Et Biophysica Acta|July 25, 1990
Oxidative phosphorylation in human muscle in patients with ocular myopathy and after general anaesthesiaH R Scholte, E Agsteribbe, H F Busch, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Experimental Cell Research|November 1, 1984
Uptake and stability of human and bovine acid alpha-glucosidase in cultured fibroblasts and skeletal muscle cells from glycogenosis type II patientsA J Reuser, M A Kroos, N J Ponne, et al.
Heart (British Cardiac Society)|March 20, 1998
The heart in limb girdle muscular dystrophyA J van der Kooi, W G de Voogt, P G Barth, et al.
International Journal of Rehabilitation Research. Internationale Zeitschrift Fur Rehabilitationsforschung. Revue Internationale De Recherches De Readaptation|October 23, 1997
Vocational perspectives and neuromuscular disordersF Andries, C W Wevers, A R Wintzen, et al.
Annals of Neurology|May 1, 1996
A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvementA J van der Kooi, T M Ledderhof, W G de Voogt, et al.
Clinical Genetics|January 1, 1981
Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency)M C Loonen, A W Schram, J F Koster, et al.
Journal of the Neurological Sciences|May 1, 1995
Differential diagnosis in spinal and bulbar muscular atrophy clinical and molecular aspectsG J Jöbsis, E S Louwerse, M de Visser, et al.
Neurology|October 1, 1981
A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studiesM C Loonen, H F Busch, J F Koster, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotypeH R Scholte, R N Van Coster, P C de Jonge, et al.
Brain : a Journal of Neurology|December 16, 1997
Miyoshi-type distal muscular dystrophy. Clinical spectrum in 24 Dutch patientsW H Linssen, N C Notermans, Y Van der Graaf, et al.
Biochimica Et Biophysica Acta|July 25, 1990
Oxidative phosphorylation in human muscle in patients with ocular myopathy and after general anaesthesiaH R Scholte, E Agsteribbe, H F Busch, et al.
Pageof 7