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H F Busch

Showing results (41-50 of 63) with videos related to

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Brain : a Journal of Neurology|December 1, 1990
Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheathsA A Gabreëls-Festen, E M Joosten, F J Gabreëls, et al.
Wiener Klinische Wochenschrift|January 6, 1989
Carnitine deficiency, mitochondrial dysfunction and the heart. Identical defect of oxidative phosphorylation in muscle mitochondria in cardiomyopathy due to carnitine loss and in Duchenne muscular dystrophyH R Scholte, R Rodrigues Pereira, H F Busch, et al.
Neurology|May 1, 1989
Congenital paucity of secondary synaptic clefts (CPSC) syndrome in 2 adult sibsJ H Wokke, F G Jennekens, P C Molenaar, et al.
Ultrastructural Pathology|September 1, 1993
Synthesis and in situ localization of lysosomal alpha-glucosidase in muscle of an unusual variant of glycogen storage disease type IIR Willemsen, A T van der Ploeg, H F Busch, et al.
Muscle & Nerve|May 8, 1998
Limb girdle muscular dystrophy: a pathological and immunohistochemical reevaluationA J van der Kooi, H B Ginjaar, H F Busch, et al.
Journal of the Neurological Sciences|December 1, 1983
Hereditary neuralgic amyotrophy. Clinical, genetic, electrophysiological and histopathological studiesW F Arts, H F Busch, H J Van den Brand, et al.
Nature Genetics|October 1, 1996
Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody diseaseA Odermatt, P E Taschner, V K Khanna, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1994
Daytime sleep in myotonic dystrophy is not caused by sleep apnoeaF G van der Meché, J M Bogaard, J C van der Sluys, et al.
The Journal of Clinical Investigation|August 1, 1994
Ca2+ homeostasis in Brody's disease. A study in skeletal muscle and cultured muscle cells and the effects of dantrolene an verapamilA A Benders, J H Veerkamp, A Oosterhof, et al.
Journal of Neurology|September 1, 1988
Prospect for enzyme therapy in glycogenosis II variants: a study on cultured muscle cellsA T van der Ploeg, P A Bolhuis, R A Wolterman, et al.
Pageof 7

Showing results (41-50 of 63) with videos related to

Sort By:
Pageof 7
Brain : a Journal of Neurology|December 1, 1990
Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheathsA A Gabreëls-Festen, E M Joosten, F J Gabreëls, et al.
Wiener Klinische Wochenschrift|January 6, 1989
Carnitine deficiency, mitochondrial dysfunction and the heart. Identical defect of oxidative phosphorylation in muscle mitochondria in cardiomyopathy due to carnitine loss and in Duchenne muscular dystrophyH R Scholte, R Rodrigues Pereira, H F Busch, et al.
Neurology|May 1, 1989
Congenital paucity of secondary synaptic clefts (CPSC) syndrome in 2 adult sibsJ H Wokke, F G Jennekens, P C Molenaar, et al.
Ultrastructural Pathology|September 1, 1993
Synthesis and in situ localization of lysosomal alpha-glucosidase in muscle of an unusual variant of glycogen storage disease type IIR Willemsen, A T van der Ploeg, H F Busch, et al.
Muscle & Nerve|May 8, 1998
Limb girdle muscular dystrophy: a pathological and immunohistochemical reevaluationA J van der Kooi, H B Ginjaar, H F Busch, et al.
Journal of the Neurological Sciences|December 1, 1983
Hereditary neuralgic amyotrophy. Clinical, genetic, electrophysiological and histopathological studiesW F Arts, H F Busch, H J Van den Brand, et al.
Nature Genetics|October 1, 1996
Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody diseaseA Odermatt, P E Taschner, V K Khanna, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1994
Daytime sleep in myotonic dystrophy is not caused by sleep apnoeaF G van der Meché, J M Bogaard, J C van der Sluys, et al.
The Journal of Clinical Investigation|August 1, 1994
Ca2+ homeostasis in Brody's disease. A study in skeletal muscle and cultured muscle cells and the effects of dantrolene an verapamilA A Benders, J H Veerkamp, A Oosterhof, et al.
Journal of Neurology|September 1, 1988
Prospect for enzyme therapy in glycogenosis II variants: a study on cultured muscle cellsA T van der Ploeg, P A Bolhuis, R A Wolterman, et al.
Pageof 7