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5. [Mitochondrial angiopathy in the cerebral blood vessels of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes)]. Ohama E, Ohara S, Ikuta F, Tanaka K, Nishizawa M, Miyatake T. No To Shinkei; 1988 Feb; 40(2):109-18. PubMed ID: 3370163 [Abstract] [Full Text] [Related]
10. 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 Feb; 12(1):38-43. PubMed ID: 8382573 [Abstract] [Full Text] [Related]
11. Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNA. Graf WD, Sumi SM, Copass MK, Ojemann LM, Longstreth WT, Shanske S, Lombes A, DiMauro S. Ann Neurol; 1993 Jun; 33(6):640-5. PubMed ID: 8388680 [Abstract] [Full Text] [Related]
18. 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]
19. [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]