A novel spinocerebellar ataxia type 15 family with involuntary movements and cognitive decline

European Journal of Neurology

Volumn 18, Issue 10, 2011, Pages 1263-1265

  Castrioto, A ^a,b   Prontera, P ^a   Di Gregorio, E ^a   Rossi, V ^a,b   Parnetti, L ^a   Rossi, A ^a   Donti, E ^a   Brusco, A ^c   Calabresi, P ^a,b   Tambasco, N ^a  

^a UNIVERSITY OF PERUGIA   (Italy)

^b IRCCS FONDAZIONE SANTA LUCIA   (Italy)

^c UNIVERSITY OF TURIN   (Italy)

Author keywords

Ataxia; Cognitive impairment; Involuntary movements; ITPR1; Spinocerebellar ataxia type 15; SUMF1

Indexed keywords

ATAXIN 1;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BALANCE IMPAIRMENT; CEREBELLAR ATAXIA; CLINICAL ARTICLE; CLINICAL EXAMINATION; CLINICAL FEATURE; COGNITIVE DEFECT; CONTROLLED STUDY; DISEASE ASSOCIATION; DYSARTHRIA; FEMALE; GENETIC SCREENING; HEREDITARY ATAXIA; HUMAN; INVOLUNTARY MOVEMENT; MALE; PRIORITY JOURNAL;

AGED; COGNITION DISORDERS; DYSARTHRIA; FEMALE; GAIT ATAXIA; GENES, DOMINANT; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS; MALE; MOVEMENT DISORDERS; PEDIGREE; SPINOCEREBELLAR ATAXIAS; SULFATASES;

EID: 80052807373     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2011.03366.x     Document Type: Article

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