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Journal Abstract Search

267 related items for PubMed ID: 22406788

  • 1. A study of familial MELAS: evaluation of A3243G mutation, clinical phenotype, and magnetic resonance spectroscopy-monitored progression.
    Chen C, Xiong N, Wang Y, Xiong J, Huang J, Zhang Z, Wang T.
    Neurol India; 2012; 60(1):86-9. PubMed ID: 22406788
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  • 2. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype.
    Kanaumi T, Hirose S, Goto Y, Naitou E, Mitsudome A.
    Pediatr Neurol; 2006 Mar; 34(3):235-8. PubMed ID: 16504796
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  • 3. Serial brain imaging analysis of stroke-like episodes in MELAS.
    Ito H, Mori K, Harada M, Minato M, Naito E, Takeuchi M, Kuroda Y, Kagami S.
    Brain Dev; 2008 Aug; 30(7):483-8. PubMed ID: 18289816
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  • 4. Diagnosis and management of MELAS.
    Thambisetty M, Newman NJ.
    Expert Rev Mol Diagn; 2004 Sep; 4(5):631-44. PubMed ID: 15347257
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  • 5. Oxidative phosphorylation defect in the brains of carriers of the tRNAleu(UUR) A3243G mutation in a MELAS pedigree.
    Dubeau F, De Stefano N, Zifkin BG, Arnold DL, Shoubridge EA.
    Ann Neurol; 2000 Feb; 47(2):179-85. PubMed ID: 10665488
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  • 11. Diversity of clinical symptoms in A3243G mitochondrial DNA mutation (MELAS syndrome mutation).
    Pronicki M, Sykut-Cegielska J, Mierzewska H, Tońska K, Karczmarewicz E, Iwanicka K, Bartnik E, Pronicka E.
    Med Sci Monit; 2002 Nov; 8(11):CR767-73. PubMed ID: 12444382
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  • 14. Steroid responsive A3243G mutation MELAS: clinical and radiographic evidence for regional hyperperfusion leading to neuronal loss.
    Walcott BP, Edlow BL, Xia Z, Kahle KT, Nahed BV, Schmahmann JD.
    Neurologist; 2012 May; 18(3):159-70. PubMed ID: 22549360
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  • 19. [MELAS syndrome masquerading as herpes encephalitis: genetic diagnosis].
    de Toledo M, Díaz-Guzmán J, Pérez-Martínez DA, Sáiz-Díaz RA, Rodríguez-Vallejo A, Campos Y.
    Rev Neurol; 2012 May; 33(2):148-50. PubMed ID: 11562875
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