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L P Rowland

Showing results (131-140 of 189) with videos related to

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Archives of Neurology|September 1, 1973
Progressive ophthalmoplegia, glycogen storage, and abnormal mitochondriaS DiMauro, D L Schotland, E Bonilla, et al.
Annals of Neurology|January 1, 1982
Juvenile spinal muscular atrophy: a new hexosaminidase deficiency phenotypeW G Johnson, H J Wigger, H R Karp, et al.
Annals of Neurology|November 1, 1983
Prognosis of ocular myastheniaC T Bever, A V Aquino, A S Penn, et al.
Journal of the Neurological Sciences|January 1, 1974
Diagnostic accuracy of clinical data, quantitative electromyography and histochemistry in neuromuscular disease. A study of 105 casesJ T Black, G P Bhatt, P V Dejesus, et al.
Neurology|November 18, 2009
Study of 962 patients indicates progressive muscular atrophy is a form of ALSW-K Kim, X Liu, J Sandner, et al.
Muscle & Nerve|February 1, 1991
Polyglucosan body diseaseM S Cafferty, R E Lovelace, A P Hays, et al.
Archives of Neurology|October 1, 1990
X-linked spinal muscular atrophy (Kennedy's syndrome). A kindred with hypobetalipoproteinemiaC L Warner, S Servidei, D J Lange, et al.
Neurology|November 30, 2000
Impact of spirituality and religiousness on outcomes in patients with ALSP L Murphy, S M Albert, C M Weber, et al.
Annals of Neurology|April 1, 1982
A benign motor neuron disorder: delayed cramps and fasciculation after poliomyelitis or myelitisM R Fetell, G Smallberg, L D Lewis, et al.
Annals of Neurology|November 1, 1995
Inclusion body myositis and myopathiesR C Griggs, V Askanas, S DiMauro, et al.
Pageof 19

Showing results (131-140 of 189) with videos related to

Sort By:
Pageof 19
Archives of Neurology|September 1, 1973
Progressive ophthalmoplegia, glycogen storage, and abnormal mitochondriaS DiMauro, D L Schotland, E Bonilla, et al.
Annals of Neurology|January 1, 1982
Juvenile spinal muscular atrophy: a new hexosaminidase deficiency phenotypeW G Johnson, H J Wigger, H R Karp, et al.
Annals of Neurology|November 1, 1983
Prognosis of ocular myastheniaC T Bever, A V Aquino, A S Penn, et al.
Journal of the Neurological Sciences|January 1, 1974
Diagnostic accuracy of clinical data, quantitative electromyography and histochemistry in neuromuscular disease. A study of 105 casesJ T Black, G P Bhatt, P V Dejesus, et al.
Neurology|November 18, 2009
Study of 962 patients indicates progressive muscular atrophy is a form of ALSW-K Kim, X Liu, J Sandner, et al.
Muscle & Nerve|February 1, 1991
Polyglucosan body diseaseM S Cafferty, R E Lovelace, A P Hays, et al.
Archives of Neurology|October 1, 1990
X-linked spinal muscular atrophy (Kennedy's syndrome). A kindred with hypobetalipoproteinemiaC L Warner, S Servidei, D J Lange, et al.
Neurology|November 30, 2000
Impact of spirituality and religiousness on outcomes in patients with ALSP L Murphy, S M Albert, C M Weber, et al.
Annals of Neurology|April 1, 1982
A benign motor neuron disorder: delayed cramps and fasciculation after poliomyelitis or myelitisM R Fetell, G Smallberg, L D Lewis, et al.
Annals of Neurology|November 1, 1995
Inclusion body myositis and myopathiesR C Griggs, V Askanas, S DiMauro, et al.
Pageof 19