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Transactions of the American Neurological Association
|
January 1, 1979
Benzodiazepine receptors in animal models of cerebellar degeneration
N Bresolin, R C Speth, T T McManus, et al.
Lancet (London, England)
|
July 25, 1987
Muscle G6PD deficiency
N Bresolin, L Bet, M Moggio, et al.
Federation Proceedings
|
July 1, 1980
Sodium-dependent, high-affinity taurine transport into rat brain synaptosomes
B A Meiners, R C Speth, N Bresolin, et al.
Enzyme
|
January 1, 1991
Glucose-6-phosphate dehydrogenase Lodi844C: a study on its expression in blood cells and muscle
P Ninfali, N Bresolin, L Baronciani, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 1, 1989
Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency
C Doriguzzi, L Palmucci, T Mongini, et al.
Neurology
|
August 1, 1986
Childhood encephalomyopathy with cytochrome c oxidase deficiency, ataxia, muscle wasting, and mental impairment
C Angelini, N Bresolin, G Pegolo, et al.
The Journal of Biological Chemistry
|
July 5, 1996
Aging-dependent functional alterations of mitochondrial DNA (mtDNA) from human fibroblasts transferred into mtDNA-less cells
K A Laderman, J R Penny, F Mazzucchelli, et al.
American Journal of Human Genetics
|
February 1, 1991
Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF)
M Zeviani, P Amati, N Bresolin, et al.
Journal of the Neurological Sciences
|
January 26, 2002
Electrophysiological analysis of cognitive slowing in subjects with mitochondrial encephalomyopathy
R Montirosso, D Brambilla, G Felisari, et al.
Neuromuscular Disorders : NMD
|
March 29, 2000
Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies
A Bardoni, G Felisari, M Sironi, et al.
Page
of 21
Search research articles
Search
Showing results (51-60 of 206) with videos related to
Sort By:
Page
of 21
Transactions of the American Neurological Association
|
January 1, 1979
Benzodiazepine receptors in animal models of cerebellar degeneration
N Bresolin, R C Speth, T T McManus, et al.
Lancet (London, England)
|
July 25, 1987
Muscle G6PD deficiency
N Bresolin, L Bet, M Moggio, et al.
Federation Proceedings
|
July 1, 1980
Sodium-dependent, high-affinity taurine transport into rat brain synaptosomes
B A Meiners, R C Speth, N Bresolin, et al.
Enzyme
|
January 1, 1991
Glucose-6-phosphate dehydrogenase Lodi844C: a study on its expression in blood cells and muscle
P Ninfali, N Bresolin, L Baronciani, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 1, 1989
Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency
C Doriguzzi, L Palmucci, T Mongini, et al.
Neurology
|
August 1, 1986
Childhood encephalomyopathy with cytochrome c oxidase deficiency, ataxia, muscle wasting, and mental impairment
C Angelini, N Bresolin, G Pegolo, et al.
The Journal of Biological Chemistry
|
July 5, 1996
Aging-dependent functional alterations of mitochondrial DNA (mtDNA) from human fibroblasts transferred into mtDNA-less cells
K A Laderman, J R Penny, F Mazzucchelli, et al.
American Journal of Human Genetics
|
February 1, 1991
Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF)
M Zeviani, P Amati, N Bresolin, et al.
Journal of the Neurological Sciences
|
January 26, 2002
Electrophysiological analysis of cognitive slowing in subjects with mitochondrial encephalomyopathy
R Montirosso, D Brambilla, G Felisari, et al.
Neuromuscular Disorders : NMD
|
March 29, 2000
Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies
A Bardoni, G Felisari, M Sironi, et al.
Page
of 21