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Human Mutation
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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 congenita
T Heiman-Patterson, C Martino, H Rosenberg, et al.
Anesthesiology
|
July 1, 1987
No relationship between fiber type and halothane contracture test results in malignant hyperthermia
T Heiman-Patterson, J E Fletcher, H Rosenberg, et al.
Muscle & Nerve
|
April 1, 1995
Myopathy, antineutrophil cytoplasmic antibodies, and glomerulonephritis
A 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 myelitis
L M Tartaglino, T Heiman-Patterson, D P Friedman, et al.
Journal of Computer Assisted Tomography
|
January 1, 1988
CT demonstration of extraocular muscle atrophy
M 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 ALS
K 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 reductase
C 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 muscle
T 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 mutation
A J Tahmoush, K L Schaller, P Zhang, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 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 congenita
T Heiman-Patterson, C Martino, H Rosenberg, et al.
Anesthesiology
|
July 1, 1987
No relationship between fiber type and halothane contracture test results in malignant hyperthermia
T Heiman-Patterson, J E Fletcher, H Rosenberg, et al.
Muscle & Nerve
|
April 1, 1995
Myopathy, antineutrophil cytoplasmic antibodies, and glomerulonephritis
A 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 myelitis
L M Tartaglino, T Heiman-Patterson, D P Friedman, et al.
Journal of Computer Assisted Tomography
|
January 1, 1988
CT demonstration of extraocular muscle atrophy
M 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 ALS
K 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 reductase
C 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 muscle
T 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 mutation
A J Tahmoush, K L Schaller, P Zhang, et al.
Page
of 4