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153 related items for PubMed ID: 8015633

  • 1. [MELAS syndrome. Clinical aspects, MRI, biochemistry and molecular genetics].
    Damian MS, Reichmann H, Seibel P, Bachmann G, Schachenmayr W, Dorndorf W.
    Nervenarzt; 1994 Apr; 65(4):258-63. PubMed ID: 8015633
    [Abstract] [Full Text] [Related]

  • 2. Clinical, pathologic and genetic studies on mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Guo Y, Guo Z, Chen L, Zhang J, Wang W, Liu X, Ren H, Gao S.
    Chin Med J (Engl); 1997 Nov; 110(11):851-5. PubMed ID: 9772417
    [Abstract] [Full Text] [Related]

  • 3. [Follow-up studies and disorders of endocrinologic function in MELAS syndrome].
    Robeck S, Stefan H, Engelhardt A, Neundörfer B.
    Nervenarzt; 1996 Jun; 67(6):465-70. PubMed ID: 8767201
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Di Trapani G, Gregori B, Servidei S, Ricci E, Sabatelli M, Tonali P.
    Clin Neuropathol; 1997 Mar; 16(4):195-200. PubMed ID: 9266144
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Clinical and autopsy findings in two cases of MELAS presenting with stroke-like episodes but without clinical myopathy.
    Nicoll JA, Moss TH, Love S, Campbell MJ, Schutt WH.
    Clin Neuropathol; 1993 Nov; 12(1):38-43. PubMed ID: 8382573
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. [MELAS syndrome as a differential diagnosis of ischemic stroke].
    Finsterer J.
    Fortschr Neurol Psychiatr; 2009 Jan; 77(1):25-31. PubMed ID: 19012224
    [Abstract] [Full Text] [Related]

  • 10. Diagnosis and management of MELAS.
    Thambisetty M, Newman NJ.
    Expert Rev Mol Diagn; 2004 Sep; 4(5):631-44. PubMed ID: 15347257
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: an autopsy report.
    Prayson RA, Wang N.
    Arch Pathol Lab Med; 1998 Nov; 122(11):978-81. PubMed ID: 9822126
    [Abstract] [Full Text] [Related]

  • 13. MELAS and L-arginine therapy: pathophysiology of stroke-like episodes.
    Koga Y, Povalko N, Nishioka J, Katayama K, Kakimoto N, Matsuishi T.
    Ann N Y Acad Sci; 2010 Jul; 1201():104-10. PubMed ID: 20649546
    [Abstract] [Full Text] [Related]

  • 14. [Evolution until death of two members of a family with A3243G mutation and MELAS phenotype versus diabetes mellitus].
    Pérez López-Fraile MI, Barrena R, Montoya J, Marta E.
    Neurologia; 2006 Jul; 21(6):327-32. PubMed ID: 16799910
    [Abstract] [Full Text] [Related]

  • 15. ["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data].
    Laforêt P, Ziegler F, Sternberg D, Rouche A, Frachon P, Fardeau M, Eymard B, Lombès A.
    Rev Neurol (Paris); 2000 Dec; 156(12):1136-47. PubMed ID: 11139730
    [Abstract] [Full Text] [Related]

  • 16. Acute hearing loss in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
    Chen JC, Tsai TC, Liu CS, Lu CT.
    Acta Neurol Taiwan; 2007 Sep; 16(3):168-72. PubMed ID: 17966957
    [Abstract] [Full Text] [Related]

  • 17. [A case of incomplete Kearns-Sayre syndrome with a stroke like episode].
    Furuya H, Sugimura T, Yamada T, Hayashi K, Kobayashi T.
    Rinsho Shinkeigaku; 1997 Aug; 37(8):680-4. PubMed ID: 9404143
    [Abstract] [Full Text] [Related]

  • 18. Myo-leukoencephalopathy in twins: study of 3243-myopathy, encephalopathy, lactic acidosis, and strokelike episodes mitochondrial DNA mutation.
    Degoul F, Diry M, Pou-Serradell A, Lloreta J, Marsac C.
    Ann Neurol; 1994 Mar; 35(3):365-70. PubMed ID: 8122891
    [Abstract] [Full Text] [Related]

  • 19. Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) in a Donegal kindred--clinical features and molecular genetic analysis.
    McEntagart M, Droogan O, Burke M, Brett F, Murphy S, Farrell M.
    Ir Med J; 1997 Mar; 90(4):144-5. PubMed ID: 9267093
    [Abstract] [Full Text] [Related]

  • 20. Depressive episode with catatonic features in a case of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Ju Seok Ryu, Sook Joung Lee, In Young Sung, Tae Sung Ko, Han Ik Yoo.
    J Child Neurol; 2009 Oct; 24(10):1307-9. PubMed ID: 19451268
    [Abstract] [Full Text] [Related]

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