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T Heiman-Patterson

Showing results (21-30 of 28) with videos related to

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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.
Neurology|June 27, 2002
High-dose cyclophosphamide without stem-cell rescue for refractory CIDPT H Brannagan, A Pradhan, T Heiman-Patterson, et al.
Blood|January 3, 2001
Posttranslational modifications of recombinant myotube-synthesized human factor IXV R Arruda, J N Hagstrom, J Deitch, et al.
Neurology|November 10, 2004
A clinical trial of creatine in ALSJ M Shefner, M E Cudkowicz, D Schoenfeld, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
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.
Neurology|June 27, 2002
High-dose cyclophosphamide without stem-cell rescue for refractory CIDPT H Brannagan, A Pradhan, T Heiman-Patterson, et al.
Blood|January 3, 2001
Posttranslational modifications of recombinant myotube-synthesized human factor IXV R Arruda, J N Hagstrom, J Deitch, et al.
Neurology|November 10, 2004
A clinical trial of creatine in ALSJ M Shefner, M E Cudkowicz, D Schoenfeld, et al.
Pageof 3