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Journal Abstract Search

258 related items for PubMed ID: 21083956

  • 1. [Unexceptional symptoms as expression of MELAS].
    van Rossum IA, ten Houten R.
    Ned Tijdschr Geneeskd; 2010; 154():A2168. PubMed ID: 21083956
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

  • 4. [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; 2007 Sep; 33(2):148-50. PubMed ID: 11562875
    [Abstract] [Full Text] [Related]

  • 5. Ketoacidosis accompanied by epileptic seizures in a patient with diabetes mellitus and mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
    Nakamura S, Yoshinari M, Wakisaka M, Kodera H, Doi Y, Yoshizumi H, Asano T, Iwase M, Mihara F, Fujishima M.
    Diabetes Metab; 2000 Nov; 26(5):407-10. PubMed ID: 11119021
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. [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 Mar; 21(6):327-32. PubMed ID: 16799910
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. 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]

  • 10. [A patient of MELAS with 3271 mutation with fatal outcome after alcohol intake].
    Shinde A, Nakano S, Taguchi Y, Kagawa D, Akiguchi I.
    Rinsho Shinkeigaku; 2000 Jun; 40(6):561-5. PubMed ID: 11086393
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Absence of maternal A3243G mtDNA mutation and reversible hyperglycemia in a patient with MELAS syndrome.
    Liou CW, Huang CC, Tsai JL, Liu JY, Pang CY, Lee HC, Wang EK, Wei YH.
    Acta Neurol Scand; 2000 Jan; 101(1):65-9. PubMed ID: 10660156
    [Abstract] [Full Text] [Related]

  • 13. Treatment options for mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.
    Santa KM.
    Pharmacotherapy; 2010 Nov; 30(11):1179-96. PubMed ID: 20973690
    [Abstract] [Full Text] [Related]

  • 14. Adult-onset of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome presenting as acute meningoencephalitis: a case report.
    Hsu YC, Yang FC, Perng CL, Tso AC, Wong LJ, Hsu CH.
    J Emerg Med; 2012 Sep; 43(3):e163-6. PubMed ID: 20036095
    [Abstract] [Full Text] [Related]

  • 15. [Exercises on a bicycle ergometer in a family of diabetes mellitus associated with a mutation of mitochondrial DNA].
    Takano M, Fujita N, Kamoi K, Makino K, Nagai H.
    Rinsho Shinkeigaku; 1998 Jul; 38(7):683-5. PubMed ID: 9868317
    [Abstract] [Full Text] [Related]

  • 16. MELAS syndrome associated with both A3243G-tRNALeu mutation and multiple mitochondrial DNA deletions.
    Aharoni S, Traves TA, Melamed E, Cohen S, Silver EL.
    J Neurol Sci; 2010 Sep 15; 296(1-2):101-3. PubMed ID: 20655066
    [Abstract] [Full Text] [Related]

  • 17. [Phenotypic variants of A3243G mitochondrial DNA mutation in a Hungarian family].
    Komlósi K, Bene J, Havasi V, Tihanyi M, Herczegfalvi A, Móser J, Melegh B.
    Orv Hetil; 2004 Aug 29; 145(35):1805-9. PubMed ID: 15493224
    [Abstract] [Full Text] [Related]

  • 18. [Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) with chronic renal failure: report of mother-child cases].
    Ihara M, Tanaka H, Yashiro M, Nishimura Y.
    Rinsho Shinkeigaku; 1996 Sep 29; 36(9):1069-73. PubMed ID: 8976130
    [Abstract] [Full Text] [Related]

  • 19. 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 29; 24(10):1307-9. PubMed ID: 19451268
    [Abstract] [Full Text] [Related]

  • 20. Intestinal pseudo-obstruction in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) associated with phenytoin therapy.
    Chiyonobu T, Noda R, Yoshida M, Fujiki A, Ishii R, Nukina S, Fujita K, Goto Y, Morimoto M.
    Brain Dev; 2008 Jun 29; 30(6):430-3. PubMed ID: 18226864
    [Abstract] [Full Text] [Related]

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