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Journal Abstract Search

155 related items for PubMed ID: 9109727

  • 21. Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycoside.
    Matsunaga T, Kumanomido H, Shiroma M, Goto Y, Usami S.
    Ann Otol Rhinol Laryngol; 2005 Feb; 114(2):153-60. PubMed ID: 15757197
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  • 23. Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome.
    Vandana VP, Bindu PS, Sonam K, Govindaraj P, Taly AB, Gayathri N, Chiplunkar S, Govindaraju C, Arvinda HR, Nagappa M, Sinha S, Thangaraj K.
    Clin Neurol Neurosurg; 2016 Sep; 148():17-21. PubMed ID: 27359089
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  • 24. 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 Sep; 48(2):150-3. PubMed ID: 24821643
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  • 25. Hearing loss caused by a P2RX2 mutation identified in a MELAS family with a coexisting mitochondrial 3243AG mutation.
    Moteki H, Azaiez H, Booth KT, Hattori M, Sato A, Sato Y, Motobayashi M, Sloan CM, Kolbe DL, Shearer AE, Smith RJ, Usami S.
    Ann Otol Rhinol Laryngol; 2015 May; 124 Suppl 1(1 0):177S-83S. PubMed ID: 25788561
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  • 26. Auditory symptoms: a critical clue for diagnosis of MELAS.
    Tawankanjanachot I, Channarong NS, Phanthumchinda K.
    J Med Assoc Thai; 2005 Nov; 88(11):1715-20. PubMed ID: 16471125
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  • 32. Audiologic and vestibular findings in a sample of human immunodeficiency virus type-1-infected Mexican children under highly active antiretroviral therapy.
    Palacios GC, Montalvo MS, Fraire MI, Leon E, Alvarez MT, Solorzano F.
    Int J Pediatr Otorhinolaryngol; 2008 Nov; 72(11):1671-81. PubMed ID: 18814921
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  • 35. Renal involvement in MELAS syndrome - a series of 5 cases and review of the literature.
    Seidowsky A, Hoffmann M, Glowacki F, Dhaenens CM, Devaux JP, de Sainte Foy CL, Provot F, Gheerbrant JD, Hummel A, Hazzan M, Dracon M, Dieux-Coeslier A, Copin MC, Noël C, Buob D.
    Clin Nephrol; 2013 Dec; 80(6):456-63. PubMed ID: 22909780
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  • 36. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].
    Goto Y.
    Nihon Rinsho; 1993 Sep; 51(9):2373-8. PubMed ID: 8411715
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