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419 related items for PubMed ID: 20036095
1. 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]
4. 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]
5. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) triggered by valproate therapy. Lam CW, Lau CH, Williams JC, Chan YW, Wong LJ. Eur J Pediatr; 1997 Jul; 156(7):562-4. PubMed ID: 9243242 [Abstract] [Full Text] [Related]
6. 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; 30(6):430-3. PubMed ID: 18226864 [Abstract] [Full Text] [Related]
8. [Unexceptional symptoms as expression of MELAS]. van Rossum IA, ten Houten R. Ned Tijdschr Geneeskd; 2010 Jun; 154():A2168. PubMed ID: 21083956 [Abstract] [Full Text] [Related]
9. 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]
10. 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]
11. 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 [Abstract] [Full Text] [Related]
12. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations]. Goto Y. Nihon Rinsho; 1993 Sep 06; 51(9):2373-8. PubMed ID: 8411715 [Abstract] [Full Text] [Related]
13. 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 06; 34(3):235-8. PubMed ID: 16504796 [Abstract] [Full Text] [Related]
14. Regression of stroke-like lesions in MELAS-syndrome after seizure control. Finsterer J, Barton P. Epileptic Disord; 2010 Dec 06; 12(4):330-4. PubMed ID: 21059492 [Abstract] [Full Text] [Related]
15. Diagnosis and management of MELAS. Thambisetty M, Newman NJ. Expert Rev Mol Diagn; 2004 Sep 06; 4(5):631-44. PubMed ID: 15347257 [Abstract] [Full Text] [Related]
16. Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report. Fukuda M, Nagao Y. J Med Case Rep; 2019 Oct 21; 13(1):313. PubMed ID: 31630688 [Abstract] [Full Text] [Related]