Brain anomalies in maternally inherited diabetes and deafness syndrome

Journal of Neurology

Volumn 256, Issue 10, 2009, Pages 1696-1704

  Fromont, I ^a   Nicoli, F ^a,b   Valero R ^a   Felician, O ^a   Lebail, B ^a   Lefur, Y ^b   Mancini, J ^a   Paquis Flucklinger, V ^c   Cozzone, P J ^b   Vialettes, Bernard ^a  

^a TIMONE HOSPITAL   (France)

^b University of Aix Marseille   (France)

^c CENTRE HOSPITALIER UNIVERSITAIRE DE NICE   (France)

Author keywords

1H MR spectroscopy; Brain dysfunction; Cerebellar atrophy; MELAS; MIDD; Mitochondrial diabetes

Indexed keywords

LACTIC ACID; N ACETYLASPARTIC ACID;

A3243G GENE; ADULT; ARTICLE; ATTENTION DEFICIT DISORDER; BRAIN FUNCTION; BRAIN MALFORMATION; CELL LOSS; CEREBELLAR ATAXIA; CEREBELLUM ATROPHY; CEREBELLUM VERMIS; CEREBROSPINAL FLUID; CLINICAL ARTICLE; CLINICAL EVALUATION; COGNITION; CONTROLLED STUDY; DISEASE ASSOCIATION; FAHR DISEASE; FEMALE; FUNCTIONAL DISEASE; GENE; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; MALE; MATERNALLY INHERITED DIABETES AND DEAFNESS; NEUROIMAGING; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; T14709G GENE; VERBAL MEMORY; WHITE MATTER; WORKING MEMORY;

EID: 70349652130     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-009-5185-4     Document Type: Article

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