Acta Neurologica Scandinavica · 2002 · 37 citations · 7 references
MedicineNeurologyNeuroscienceNeuropathologyNeuropsychiatryNeuropsychologyCognitive ImpairmentExecutive DysfunctionNeurocognitive DisordersNeurodegenerative DiseasesNeurodegenerative DisordersStrokeAlertnessBasal Ganglia LesionsLactate AcidosisLactic AcidosisMelas SyndromeMitochondrial Cognitive ImpairmentMitochondrial EncephalomyopathyNeurocognitive Impairment
Sartor H, Loose R, Tucha O, Klein HE, Lange KW. MELAS: a neuropsychological and radiological follow-up study. Acta Neurol Scand 2002; 106: 309–313. © Blackwell Munksgaard 2002. We report on a patient with long standing, full-blown mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS). In contrast to earlier publications, detailed neuropsychological assessment revealed no dementia but a pattern of distinct cognitive deficits with marked impairment of visuo-constructive and executive functions. Focal lesions and progressing atrophy mainly of the basal ganglia and the temporo-parieto-occipital area with preservation of hippocampal and entorhinal structures were present. Furthermore, a 4-year follow-up assessment revealed an increasing deterioration of distinct cognitive functions, including phasic alertness, tactile functions and the discrimination of tone pitch and rhythm. This may be because of chronic regional metabolic disturbances, as there was no further stroke-like episode in that period of time.
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Integration of diverse information in working memory within the frontal lobe
Vivek Prabhakaran, K. K. Narayanan, Zhixiang Zhao et al. · Nature Neuroscience · 2000 · 547 citations
Mitochondrial encephalomyopathy (MELAS) with mental disorder
Tohru Suzuki, J Koizumi, Hiroyasu Shiraishi et al. · Neuroradiology · 1990 · 62 citations