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T Heiman

Showing results (21-30 of 33) with videos related to

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Clinical Orthopaedics and Related Research|September 1, 1985
Muscle biopsy: proper surgical techniqueA T Berman, J L Garbarino, H Rosenberg, et al.
Neurology|June 1, 1996
Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working groupJ K Fink, T Heiman-Patterson, T Bird, et al.
Journal of Medical Genetics|November 6, 2001
Hereditary spastic paraplegia linked to chromosome 14q11-q21: reduction of the SPG3 locus interval from 5.3 to 2.7 cMS Rainier, P Hedera, D Alvarado, et al.
Neurology|May 1, 1990
Lower motor neuron disease in a patient with autoantibodies against Gal(beta 1-3)GalNAc in gangliosides GM1 and GD1b: improvement following immunotherapyM E Shy, T Heiman-Patterson, G J Parry, et al.
Neurology|September 27, 2006
High-frequency chest wall oscillation in ALS: an exploratory randomized, controlled trialD J Lange, N Lechtzin, C Davey, et al.
Annals of Surgery|October 1, 1993
Techniques to enhance extramyocardial collateral blood flow after a cardiomyoplastyJ D Mannion, M Magno, P Buckman, et al.
Anesthesiology|May 1, 1995
Masseter muscle rigidity associated with glycine1306-to-alanine mutation in the adult muscle sodium channel alpha-subunit geneG M Vita, A Olckers, A E Jedlicka, et al.
Annals of Neurology|May 1, 1989
Antibodies to GM1 and GD1b in patients with motor neuron disease without plasma cell dyscrasiaM E Shy, V A Evans, F D Lublin, et al.
Science (New York, N.Y.)|March 18, 1988
Duchenne muscular dystrophy gene expression in normal and diseased human muscleM O Scott, J E Sylvester, T Heiman-Patterson, et al.
Nature Genetics|October 31, 2001
Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegiaX Zhao, D Alvarado, S Rainier, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Clinical Orthopaedics and Related Research|September 1, 1985
Muscle biopsy: proper surgical techniqueA T Berman, J L Garbarino, H Rosenberg, et al.
Neurology|June 1, 1996
Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working groupJ K Fink, T Heiman-Patterson, T Bird, et al.
Journal of Medical Genetics|November 6, 2001
Hereditary spastic paraplegia linked to chromosome 14q11-q21: reduction of the SPG3 locus interval from 5.3 to 2.7 cMS Rainier, P Hedera, D Alvarado, et al.
Neurology|May 1, 1990
Lower motor neuron disease in a patient with autoantibodies against Gal(beta 1-3)GalNAc in gangliosides GM1 and GD1b: improvement following immunotherapyM E Shy, T Heiman-Patterson, G J Parry, et al.
Neurology|September 27, 2006
High-frequency chest wall oscillation in ALS: an exploratory randomized, controlled trialD J Lange, N Lechtzin, C Davey, et al.
Annals of Surgery|October 1, 1993
Techniques to enhance extramyocardial collateral blood flow after a cardiomyoplastyJ D Mannion, M Magno, P Buckman, et al.
Anesthesiology|May 1, 1995
Masseter muscle rigidity associated with glycine1306-to-alanine mutation in the adult muscle sodium channel alpha-subunit geneG M Vita, A Olckers, A E Jedlicka, et al.
Annals of Neurology|May 1, 1989
Antibodies to GM1 and GD1b in patients with motor neuron disease without plasma cell dyscrasiaM E Shy, V A Evans, F D Lublin, et al.
Science (New York, N.Y.)|March 18, 1988
Duchenne muscular dystrophy gene expression in normal and diseased human muscleM O Scott, J E Sylvester, T Heiman-Patterson, et al.
Nature Genetics|October 31, 2001
Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegiaX Zhao, D Alvarado, S Rainier, et al.
Pageof 4