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Brain : a Journal of Neurology
|
December 1, 1990
Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths
A 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 dystrophy
H 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 sibs
J 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 II
R Willemsen, A T van der Ploeg, H F Busch, et al.
Muscle & Nerve
|
May 8, 1998
Limb girdle muscular dystrophy: a pathological and immunohistochemical reevaluation
A 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 studies
W 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 disease
A 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 apnoea
F 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 verapamil
A 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 cells
A T van der Ploeg, P A Bolhuis, R A Wolterman, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 63) with videos related to
Sort By:
Page
of 7
Brain : a Journal of Neurology
|
December 1, 1990
Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths
A 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 dystrophy
H 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 sibs
J 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 II
R Willemsen, A T van der Ploeg, H F Busch, et al.
Muscle & Nerve
|
May 8, 1998
Limb girdle muscular dystrophy: a pathological and immunohistochemical reevaluation
A 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 studies
W 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 disease
A 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 apnoea
F 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 verapamil
A 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 cells
A T van der Ploeg, P A Bolhuis, R A Wolterman, et al.
Page
of 7