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Journal Abstract Search

234 related items for PubMed ID: 16413582

  • 21. Association of alpha-synuclein immunoreactivity with inflammatory activity in multiple sclerosis lesions.
    Lu JQ, Fan Y, Mitha AP, Bell R, Metz L, Moore GR, Yong VW.
    J Neuropathol Exp Neurol; 2009 Feb; 68(2):179-89. PubMed ID: 19151622
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  • 22. [A patient with bilateral lesion in the striatum and slowly progressive dystonia secondary to T14487C mutation in the ND6 gene of complex I of the mitochondrial respiratory chain].
    Raspall-Chaure M, Solano A, Vázquez E, Macaya-Ruiz A, del Toro-Riera M, Cabezuelo-Briones A, Montoya J, Andreu A, Roig-Quilis M.
    Rev Neurol; 2009 Feb; 39(12):1129-32. PubMed ID: 15625630
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  • 23. The mitochondrial connection in auditory neuropathy.
    Cacace AT, Pinheiro JM.
    Audiol Neurootol; 2011 Feb; 16(6):398-413. PubMed ID: 21266802
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  • 25. Chronic corticosteroid administration causes mitochondrial dysfunction in skeletal muscle.
    Mitsui T, Azuma H, Nagasawa M, Iuchi T, Akaike M, Odomi M, Matsumoto T.
    J Neurol; 2002 Aug; 249(8):1004-9. PubMed ID: 12195445
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  • 29. Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophy.
    Verny C, Loiseau D, Scherer C, Lejeune P, Chevrollier A, Gueguen N, Guillet V, Dubas F, Reynier P, Amati-Bonneau P, Bonneau D.
    Neurology; 2008 Mar 25; 70(13 Pt 2):1152-3. PubMed ID: 18287570
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  • 39. Mitochondrial respiratory complex I deficiency simulating spinal muscular atrophy.
    Lee JS, Hwang JS, Ryu KH, Lee EH, Kim SH.
    Pediatr Neurol; 2007 Jan 25; 36(1):45-7. PubMed ID: 17162196
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  • 40. Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient.
    Blázquez A, Gil-Borlado MC, Morán M, Verdú A, Cazorla-Calleja MR, Martín MA, Arenas J, Ugalde C.
    Neuromuscul Disord; 2009 Feb 25; 19(2):143-6. PubMed ID: 19162478
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