Mitochondrial disorders

Citations 41-50 of 92 total displayed.

Past content (since Mar 2001):

BRIEF COMMUNICATIONS
L-Arginine improves the symptoms of strokelike episodes in MELAS

Y. Koga, Y. Akita, J. Nishioka, S. Yatsuga, N. Povalko, Y. Tanabe, S. Fujimoto, and Toyojiro Matsuishi
Neurology 2005; 64: 710-712. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Coenzyme Q deficiency and cerebellar ataxia associated with an aprataxin mutation

C. M. Quinzii, A. G. Kattah, A. Naini, H. O. Akman, V. K. Mootha, S. DiMauro, and M. Hirano
Neurology 2005; 64: 539-541. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicism

G. Hudson, M. Deschauer, K. Busse, S. Zierz, and P. F. Chinnery
Neurology 2005; 64: 371-373. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
[¹²³I]FP-CIT SPECT findings in two patients with Hallervorden–Spatz disease with homozygous mutation in PANK2 gene

G. Cossu, C. Cella, M. Melis, A. Antonini, G. L. Floris, L. Ruffini, and A. Spissu
Neurology 2005; 64: 167-168. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIE

M. A. Martín, A. Blázquez, R. Martí, J. Bautista, M. C. Lara, A. Cabello, Y. Campos, O. Belda, A. L. Andreu, and J. Arenas
Neurology 2004; 63: 1536-1537. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Juvenile form of Alexander disease with GFAP mutation and mitochondrial abnormality

Y. Nobuhara, K. Nakahara, I. Higuchi, T. Yoshida, S. Fushiki, M. Osame, K. Arimura, and M. Nakagawa
Neurology 2004; 63: 1302-1304. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Mitochondrial DNA nucleotide changes in non-arteritic ischemic optic neuropathy

Thomas M. Bosley, Khaled K. Abu-Amero, and Pinar T. Ozand
Neurology 2004; 63: 1305-1308. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Progression despite replacement of a myopathic form of coenzyme Q₁₀ defect

K. Auré, J. F. Benoist, H. Ogier de Baulny, N. B. Romero, O. Rigal, and A. Lombès
Neurology 2004; 63: 727-729. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
A novel mitochondrial tRNA^Phe mutation causes MERRF syndrome

M. Mancuso, M. Filosto, V. K. Mootha, A. Rocchi, S. Pistolesi, L. Murri, S. DiMauro, and G. Siciliano
Neurology 2004; 62: 2119-2121. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Late-onset Leigh syndrome in a patient with mitochondrial complex I NDUFS8 mutations

Vincent Procaccio and Douglas C. Wallace
Neurology 2004; 62: 1899-1901. [Abstract] [Full text] [PDF]  

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