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Journal Abstract Search

570 related items for PubMed ID: 20973690

  • 1. 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
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  • 4. Chorea-ballism as a dominant clinical manifestation in heteroplasmic mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes syndrome with A3251G mutation in mitochondrial genome: a case report.
    Lahiri D, Sawale VM, Banerjee S, Dubey S, Roy BK, Das SK.
    J Med Case Rep; 2019 Mar 06; 13(1):63. PubMed ID: 30837005
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  • 5. 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 06; 1201():104-10. PubMed ID: 20649546
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  • 7. Beneficial effect of L-arginine for stroke-like episode in MELAS.
    Kubota M, Sakakihara Y, Mori M, Yamagata T, Momoi-Yoshida M.
    Brain Dev; 2004 Oct 06; 26(7):481-3; discussion 480. PubMed ID: 15351086
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  • 10. The mitochondrial myopathy encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome: a review of treatment options.
    Scaglia F, Northrop JL.
    CNS Drugs; 2006 Oct 06; 20(6):443-64. PubMed ID: 16734497
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  • 12. [MELAS--mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome--two cases confirmed by biochemical and molecular investigations. Differential diagnosis of stroke causes].
    Mierzewska H, Mroczek K, Pronicki M, Pronicka E, Karczmarewicz E, Bartnik E, Zdzienicka E, Seniów J, Schmidt-Sidor B, Taraszewska A, Palasik W.
    Neurol Neurochir Pol; 2002 Oct 06; 36(3):457-70. PubMed ID: 12185802
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  • 15. 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 06; 30(6):430-3. PubMed ID: 18226864
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  • 16. [MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes)].
    Goto Y.
    Ryoikibetsu Shokogun Shirizu; 2001 Jun 06; (36):146-9. PubMed ID: 11596349
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  • 17. 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 06; 35(3):365-70. PubMed ID: 8122891
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  • 18. Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disorders.
    Mimaki M, Hatakeyama H, Ichiyama T, Isumi H, Furukawa S, Akasaka M, Kamei A, Komaki H, Nishino I, Nonaka I, Goto Y.
    Mitochondrion; 2009 Apr 06; 9(2):115-22. PubMed ID: 19460299
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  • 19. Wolff-Parkinson-White syndrome in Patients With MELAS.
    Sproule DM, Kaufmann P, Engelstad K, Starc TJ, Hordof AJ, De Vivo DC.
    Arch Neurol; 2007 Nov 06; 64(11):1625-7. PubMed ID: 17998445
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  • 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 06; 24(10):1307-9. PubMed ID: 19451268
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