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Results: 1-25/454
Authors:
Pascuzzi, RM
Citation: Rm. Pascuzzi, Mitochondrial disorders - Introduction of John M. Shoffner, SEM NEUROL, 21(3), 2001, pp. 231-231
Authors:
Shoffner, JM
Citation: Jm. Shoffner, Mitochondrial disorders - Preface, SEM NEUROL, 21(3), 2001, pp. 233-234
Authors:
Shoffner, JM
Citation: Jm. Shoffner, An introduction: Oxidative phosphorylation diseases, SEM NEUROL, 21(3), 2001, pp. 237-250
Authors:
DiMauro, S
Andreu, AL
Musumeci, O
Bonilla, E
Citation: S. Dimauro et al., Diseases of oxidative phosphorylation due to mtDNA mutations, SEM NEUROL, 21(3), 2001, pp. 251-260
Authors:
Shoubridge, EA
Citation: Ea. Shoubridge, Nuclear gene defects in respiratory chain disorders, SEM NEUROL, 21(3), 2001, pp. 261-267
Authors:
Robinson, BH
Citation: Bh. Robinson, Prenatal diagnosis of disorders of energy metabolism, SEM NEUROL, 21(3), 2001, pp. 269-273
Authors:
Biousse, V
Newman, NJ
Citation: V. Biousse et Nj. Newman, Neuro-ophthalmology of mitochondrial diseases, SEM NEUROL, 21(3), 2001, pp. 275-291
Authors:
Sladky, JT
Citation: Jt. Sladky, Histopathological features of peripheral nerve and muscle in mitochondrialdisease, SEM NEUROL, 21(3), 2001, pp. 293-301
Authors:
Dougherty, FE
Citation: Fe. Dougherty, Metabolic testing in mitochondrial disease, SEM NEUROL, 21(3), 2001, pp. 303-308
Authors:
Gold, DR
Cohen, BH
Citation: Dr. Gold et Bh. Cohen, Treatment of mitochondrial cytopathies, SEM NEUROL, 21(3), 2001, pp. 309-325
Authors:
Zullo, SJ
Citation: Sj. Zullo, Gene therapy of mitochondrial DNA mutations: A brief, biased history of allotopic expression in mammalian cells, SEM NEUROL, 21(3), 2001, pp. 327-335
Authors:
Krawiecki, N
Citation: N. Krawiecki, Ethical issues surrounding the evaluation of oxidative phosphorylation disorders in children, SEM NEUROL, 21(3), 2001, pp. 337-341
Authors:
Pascuzzi, RM
Citation: Rm. Pascuzzi, Introduction of Wim Robberecht, SEM NEUROL, 21(2), 2001, pp. 125-125
Authors:
Robberecht, W
Citation: W. Robberecht, Motor neuron diseases - Preface, SEM NEUROL, 21(2), 2001, pp. 127-127
Authors:
Brown, RH
Robberecht, W
Citation: Rh. Brown et W. Robberecht, Amyotrophic lateral sclerosis: Pathogenesis, SEM NEUROL, 21(2), 2001, pp. 131-139
Authors:
Eisen, A
Citation: A. Eisen, Clinical electrophysiology of the upper and lower motor neuron in amyotrophic lateral sclerosis, SEM NEUROL, 21(2), 2001, pp. 141-154
Authors:
Borasio, GD
Miller, RG
Citation: Gd. Borasio et Rg. Miller, Clinical characteristics and management of ALS, SEM NEUROL, 21(2), 2001, pp. 155-166
Authors:
Turner, MR
Parton, MJ
Leigh, PN
Citation: Mr. Turner et al., Clinical trials in ALS: An overview, SEM NEUROL, 21(2), 2001, pp. 167-175
Authors:
Verma, A
Bradley, WG
Citation: A. Verma et Wg. Bradley, Atypical motor neuron disease and related motor syndromes, SEM NEUROL, 21(2), 2001, pp. 177-187
Authors:
Talbot, K
Davies, KE
Citation: K. Talbot et Ke. Davies, Spinal muscular atrophy, SEM NEUROL, 21(2), 2001, pp. 189-197
Authors:
Fink, JK
Citation: Jk. Fink, Progressive spastic paraparesis: Hereditary spastic paraplegia and its relation to primary and amyotrophic lateral sclerosis, SEM NEUROL, 21(2), 2001, pp. 199-207
Authors:
Arevalo, J
Wojcieszek, J
Conneally, PM
Citation: J. Arevalo et al., Tracing Woody Guthrie and Huntington's disease, SEM NEUROL, 21(2), 2001, pp. 209-223
Authors:
Pascuzzi, RM
Citation: Rm. Pascuzzi, Introduction of Nestor Galvez-Jimenez, SEM NEUROL, 21(1), 2001, pp. 1-1
Authors:
Galvez-Jimenez, N
Citation: N. Galvez-jimenez, Movement disorders - Preface, SEM NEUROL, 21(1), 2001, pp. 3-5
Authors:
Tuite, P
Ebbitt, B
Citation: P. Tuite et B. Ebbitt, Dopamine agonists, SEM NEUROL, 21(1), 2001, pp. 9-14