Impaired body movement representation in DYT1 mutation carriers

Clinical Neurophysiology

Volumn 119, Issue 8, 2008, Pages 1864-1869

  Fiorio, M ^a   Gambarin, M ^a   Defazio, G ^b   Valente, E M ^c,d   Stanzani, C ^a   Moretto, G ^e   Loi, M ^f   Soliveri, P ^g   Nardocci, N ^g   Albanese, A ^g   Fiaschi, A ^a   Tinazzi, M ^a,e  

^a UNIVERSITY OF VERONA   (Italy)

^b UNIVERSITY OF BARI   (Italy)

^c Mendel Institute   (Italy)

^d UNIVERSITY OF MESSINA   (Italy)

^e BORGO TRENTO HOSPITAL   (Italy)

^f BROTZU HOSPITAL   (Italy)

^g National Neurological Institute   (Italy)

Author keywords

Dystonia; DYT1 gene; Endophenotype; Mental rotation; Movement representation

Indexed keywords

ADULT; AGED; ARTICLE; BODY MOVEMENT; CLINICAL ARTICLE; COGNITION; DYT1 GENE; FEMALE; GENE; GENE DELETION; GENE MUTATION; HETEROZYGOTE; HUMAN; MALE; MOTOR CONTROL; MOTOR PERFORMANCE; NERVE CELL NETWORK; PENETRANCE; PLANNING; PRIORITY JOURNAL; RESPONSE TIME; SCHOOL CHILD; SIMULATION; TORSION DYSTONIA;

ADOLESCENT; ADULT; AGED; ANALYSIS OF VARIANCE; CHILD; DNA MUTATIONAL ANALYSIS; DYSTONIA; FEMALE; FUNCTIONAL LATERALITY; HUMANS; MALE; MIDDLE AGED; MOLECULAR CHAPERONES; MOVEMENT; MUTATION; ORIENTATION; PHOTIC STIMULATION; POSTURE; PSYCHOMOTOR PERFORMANCE; REACTION TIME; TRINUCLEOTIDE REPEATS;

EID: 46049096077     PISSN: 13882457     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clinph.2008.04.292     Document Type: Article

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