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V Askanas

Showing results (131-140 of 141) with videos related to

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The American Journal of Pathology|April 18, 1998
Light and electron microscopic immunolocalization of presenilin 1 in abnormal muscle fibers of patients with sporadic inclusion-body myositis and autosomal-recessive inclusion-body myopathyV Askanas, W K Engel, C C Yang, et al.
Ophthalmology|April 1, 1981
Systemic manifestations of gyrate atrophy of the choroid and retinaM I Kaiser-Kupfer, T Kuwabara, V Askanas, et al.
Annals of Neurology|November 1, 1995
Inclusion body myositis and myopathiesR C Griggs, V Askanas, S DiMauro, et al.
The Journal of Clinical Investigation|October 1, 1993
Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiencyA Martinuzzi, L Vergani, R Carrozzo, et al.
Neurology|February 13, 2002
Three lipoprotein receptors and cholesterol in inclusion-body myositis muscleM Jaworska-Wilczynska, G M Wilczynski, W K Engel, et al.
Journal of Neurocytology|August 1, 1987
De novo neuromuscular junction formation on human muscle fibres cultured in monolayer and innervated by foetal rat spinal cord: ultrastructural and ultrastructural--cytochemical studiesV Askanas, H Kwan, R B Alvarez, et al.
Annals of Neurology|August 1, 1996
Apolipoprotein E alleles in sporadic inclusion-body myositis and hereditary inclusion-body myopathyV Askanas, W K Engel, M Mirabella, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Mitochondrial DNA variants in inclusion body myositisC C Kok, A Boyt, S Gaudieri, et al.
Neurology|January 1, 1985
Autosomal dominant syndrome of lipid neuromyopathy with normal carnitine: successful treatment with long-chain fatty-acid-free dietV Askanas, W K Engel, H H Kwan, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2001
Muscle-specific mutations accumulate with aging in critical human mtDNA control sites for replicationY Wang, Y Michikawa, C Mallidis, et al.
Pageof 15

Showing results (131-140 of 141) with videos related to

Sort By:
Pageof 15
The American Journal of Pathology|April 18, 1998
Light and electron microscopic immunolocalization of presenilin 1 in abnormal muscle fibers of patients with sporadic inclusion-body myositis and autosomal-recessive inclusion-body myopathyV Askanas, W K Engel, C C Yang, et al.
Ophthalmology|April 1, 1981
Systemic manifestations of gyrate atrophy of the choroid and retinaM I Kaiser-Kupfer, T Kuwabara, V Askanas, et al.
Annals of Neurology|November 1, 1995
Inclusion body myositis and myopathiesR C Griggs, V Askanas, S DiMauro, et al.
The Journal of Clinical Investigation|October 1, 1993
Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiencyA Martinuzzi, L Vergani, R Carrozzo, et al.
Neurology|February 13, 2002
Three lipoprotein receptors and cholesterol in inclusion-body myositis muscleM Jaworska-Wilczynska, G M Wilczynski, W K Engel, et al.
Journal of Neurocytology|August 1, 1987
De novo neuromuscular junction formation on human muscle fibres cultured in monolayer and innervated by foetal rat spinal cord: ultrastructural and ultrastructural--cytochemical studiesV Askanas, H Kwan, R B Alvarez, et al.
Annals of Neurology|August 1, 1996
Apolipoprotein E alleles in sporadic inclusion-body myositis and hereditary inclusion-body myopathyV Askanas, W K Engel, M Mirabella, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Mitochondrial DNA variants in inclusion body myositisC C Kok, A Boyt, S Gaudieri, et al.
Neurology|January 1, 1985
Autosomal dominant syndrome of lipid neuromyopathy with normal carnitine: successful treatment with long-chain fatty-acid-free dietV Askanas, W K Engel, H H Kwan, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2001
Muscle-specific mutations accumulate with aging in critical human mtDNA control sites for replicationY Wang, Y Michikawa, C Mallidis, et al.
Pageof 15