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Journal Abstract Search

152 related items for PubMed ID: 17664998

  • 1. Screening for MELAS mutations in young patients with stroke of undetermined origin.
    Conforto AB, Yamamoto FI, Oba-Shinjo SM, Pinto JG, Hoshino M, Scaff M, Marie SK.
    Arq Neuropsiquiatr; 2007 Jun; 65(2B):371-6. PubMed ID: 17664998
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  • 2. Clinical and genetic features in two families with MELAS and the T3271C mutation in mitochondrial DNA.
    Tay SK, Shanske S, Crowe C, Shanske A, Schafer I, Pancrudo J, Lu J, Bonilla E, DiMauro S.
    J Child Neurol; 2005 Feb; 20(2):142-6. PubMed ID: 15794182
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  • 3. Heterogeneous phenotypic manifestations of maternally inherited deafness associated with the mitochondrial A3243G mutation. Case report.
    Hoptasz M, Szczuciński A, Losy J.
    Neurol Neurochir Pol; 2014 Feb; 48(2):150-3. PubMed ID: 24821643
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  • 15. Diagnosis of adult-onset MELAS syndrome in a 63-year-old patient with suspected recurrent strokes - a case report.
    Sinnecker T, Andelova M, Mayr M, Rüegg S, Sinnreich M, Hench J, Frank S, Schaller A, Stippich C, Wuerfel J, Bonati LH.
    BMC Neurol; 2019 May 08; 19(1):91. PubMed ID: 31068171
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  • 19. High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families.
    Cevoli S, Pallotti F, La Morgia C, Valentino ML, Pierangeli G, Cortelli P, Baruzzi A, Montagna P, Carelli V.
    Cephalalgia; 2010 Aug 08; 30(8):919-27. PubMed ID: 20656703
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