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searching for MELAS syndrome 7 found (30 total)

Mitochondrial encephalomyopathy (1,740 words) [view diff] exact match in snippet view article find links to article

problems with movement or controlling muscles. Between 40 and 90% of MELAS syndrome patients are reported to develop dementia, and epilepsy is seen in 71–96%

MT-TH (964 words) [view diff] exact match in snippet view article find links to article

consciousness, seizures, and other problems affecting the nervous system. MELAS syndrome may also be accompanied by another mitochondrial disorder called myoclonic

MT-TK (1,373 words) [view diff] exact match in snippet view article find links to article

family with the syndrome exhibited mutations of 3243A>G and 16428G>A. MELAS syndrome may also be accompanied by another mitochondrial disorder called myoclonic

Degenerative disease (1,637 words) [view diff] case mismatch in snippet view article find links to article

1016/j.arr.2009.09.001. ISSN 1568-1637. PMID 19772952. S2CID 205666350. "MELAS Syndrome". NORD (National Organization for Rare Disorders). Archived from the

MT-ND4 (2,131 words) [view diff] no match in snippet view article find links to article

mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I". American Journal

Joanna Poulton (1,447 words) [view diff] exact match in snippet view article find links to article

Poulton, Joanna; Morten, Karl (July 1993). "Noninvasive diagnosis of the MELAS syndrome from blood DNA". Annals of Neurology. 34 (1): 116. doi:10.1002/ana.410340124

Koreans (8,242 words) [view diff] exact match in snippet view article find links to article

1086/444436. PMC 1226206. PMID 16080116. Hwang, Jung-Hee (20 June 2008). "A MELAS syndrome family harboring two mutations in mitochondrial genome". Experimental