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T Heiman

Showing results (11-20 of 33) with videos related to

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Human Mutation|January 1, 1995
Two novel missense mutations (E654K, L396P) in Caucasian patients with myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, A Martinuzzi, et al.
Neurology|May 1, 1988
Malignant hyperthermia in myotonia congenitaT Heiman-Patterson, C Martino, H Rosenberg, et al.
Anesthesiology|July 1, 1987
No relationship between fiber type and halothane contracture test results in malignant hyperthermiaT Heiman-Patterson, J E Fletcher, H Rosenberg, et al.
Muscle & Nerve|April 1, 1995
Myopathy, antineutrophil cytoplasmic antibodies, and glomerulonephritisA J Tahmoush, J E Liu, M S Amir, et al.
AJNR. American Journal of Neuroradiology|March 1, 1995
MR imaging in a case of postvaccination myelitisL M Tartaglino, T Heiman-Patterson, D P Friedman, et al.
Journal of Computer Assisted Tomography|January 1, 1988
CT demonstration of extraocular muscle atrophyM L Hansman, R G Peyster, T Heiman-Patterson, et al.
Journal of the Neurological Sciences|June 29, 1999
Bipap improves survival and rate of pulmonary function decline in patients with ALSK A Kleopa, M Sherman, B Neal, et al.
The Biochemical Journal|January 22, 2000
Cellular adaptation to down-regulated iron transport into lymphoid leukaemic cells: effects on the expression of the gene for ribonucleotide reductaseC R Chitambar, J P Wereley, T Heiman, et al.
Journal of the Neurological Sciences|December 1, 1993
Anti-GM1/GD1b M-proteins damage human spinal cord neurons co-cultured with muscleT Heiman-Patterson, T Krupa, P Thompson, et al.
Neuromuscular Disorders : NMD|September 1, 1994
Muscle sodium channel inactivation defect in paramyotonia congenita with the thr1313met mutationA J Tahmoush, K L Schaller, P Zhang, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Human Mutation|January 1, 1995
Two novel missense mutations (E654K, L396P) in Caucasian patients with myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, A Martinuzzi, et al.
Neurology|May 1, 1988
Malignant hyperthermia in myotonia congenitaT Heiman-Patterson, C Martino, H Rosenberg, et al.
Anesthesiology|July 1, 1987
No relationship between fiber type and halothane contracture test results in malignant hyperthermiaT Heiman-Patterson, J E Fletcher, H Rosenberg, et al.
Muscle & Nerve|April 1, 1995
Myopathy, antineutrophil cytoplasmic antibodies, and glomerulonephritisA J Tahmoush, J E Liu, M S Amir, et al.
AJNR. American Journal of Neuroradiology|March 1, 1995
MR imaging in a case of postvaccination myelitisL M Tartaglino, T Heiman-Patterson, D P Friedman, et al.
Journal of Computer Assisted Tomography|January 1, 1988
CT demonstration of extraocular muscle atrophyM L Hansman, R G Peyster, T Heiman-Patterson, et al.
Journal of the Neurological Sciences|June 29, 1999
Bipap improves survival and rate of pulmonary function decline in patients with ALSK A Kleopa, M Sherman, B Neal, et al.
The Biochemical Journal|January 22, 2000
Cellular adaptation to down-regulated iron transport into lymphoid leukaemic cells: effects on the expression of the gene for ribonucleotide reductaseC R Chitambar, J P Wereley, T Heiman, et al.
Journal of the Neurological Sciences|December 1, 1993
Anti-GM1/GD1b M-proteins damage human spinal cord neurons co-cultured with muscleT Heiman-Patterson, T Krupa, P Thompson, et al.
Neuromuscular Disorders : NMD|September 1, 1994
Muscle sodium channel inactivation defect in paramyotonia congenita with the thr1313met mutationA J Tahmoush, K L Schaller, P Zhang, et al.
Pageof 4