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Journal Abstract Search

70 related items for PubMed ID: 9124815

  • 1. Complex I function in familial and sporadic dystonia.
    Schapira AH, Warner T, Gash MT, Cleeter MW, Marinho CF, Cooper JM.
    Ann Neurol; 1997 Apr; 41(4):556-9. PubMed ID: 9124815
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  • 4. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
    Pénisson-Besnier I, Moreau C, Jacques C, Roger JC, Dubas F, Reynier P.
    Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773
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  • 12. Electron transfer complex I defect in idiopathic dystonia.
    Benecke R, Strümper P, Weiss H.
    Ann Neurol; 1992 Nov; 32(5):683-6. PubMed ID: 1449249
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  • 14. Diagnostic potential of mitochondrial DNA assessment in patients with optic neuropathy.
    Feng X, Pu W, Gao D, Isashiki Y, Ohba N.
    Chin Med J (Engl); 2000 Aug; 113(8):743-6. PubMed ID: 11776061
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  • 16. [Diagnostic and differential diagnostic potential of mitochondrial DNA assessment in patients with Leber's hereditary optic neuropathy].
    Feng X, Pu W, Gao D.
    Zhonghua Yan Ke Za Zhi; 2001 May; 37(3):174-7. PubMed ID: 11864415
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