Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification

Brain

Volumn 136, Issue 11, 2013, Pages 3395-3407

  Nicolas, Gaël ^a,b,c,d   Pottier, Cyril ^a,c,d   Charbonnier, Camille ^d   Guyant Maréchal, Lucie ^b   Le Ber, Isabelle ^a   Pariente, Jérémie ^e   Labauge, Pierre ^f   Ayrignac, Xavier ^f   Defebvre, Luc ^g   Maltête, David ^a,b,c   Martinaud, Olivier ^b,d   Lefaucheur, Romain ^b   Guillin, Olivier ^a,c,h   Wallon, David ^a,b,c,d   Chaumette, Boris ^h   Rondepierre, Philippe ⁱ   Derache, Nathalie ^j   Fromager, Guillaume ^j   Schaeffer, Stéphane ^j   Krystkowiak, Pierre ^k   Verny, Christophe ^l   Jurici, Snejana ^m   Sauvée, Mathilde ⁿ   Vérin, Marc ^o   Lebouvier, Thibaud ^p   Rouaud, Olivier ^q   Thauvin Robinet, Christel ^r   Rousseau, Stéphane ^a,c,d   Rovelet Lecrux, Anne ^a,c,d   Frebourg, Thierry ^a,b,c   Campion, Dominique ^a,c,d,s   Hannequin, Didier ^a,b,c,d   more..

^a INSERM   (France)

^b ROUEN UNIVERSITY HOSPITAL   (France)

^c UNIVERSITY OF ROUEN   (France)

^d Lille and Paris Salpêtrière University Hospitals   (France)

^e TOULOUSE UNIVERSITY HOSPITAL   (France)

^f MONTPELLIER UNIVERSITY HOSPITAL   (France)

^g LILLE UNIVERSITY HOSPITAL   (France)

^h Sotteville Lès Rouen   (France)

ⁱ Dreux Hospital   (France)

^j CAEN UNIVERSITY HOSPITAL   (France)

^k AMIENS UNIVERSITY HOSPITAL   (France)

^l ANGERS UNIVERSITY HOSPITAL   (France)

^m Perpignan Hospital   (France)

ⁿ UNIVERSITY HOSPITAL OF NANCY   (France)

^o PONTCHAILLOU UNIVERSITY HOSPITAL   (France)

^p NANTES UNIVERSITY HOSPITAL   (France)

^q DIJON UNIVERSITY HOSPITAL   (France)

^r Medical University of Dijon   (France)

^s Rouvray Psychiatric Hospital   (France)

more..

Author keywords

Ageing; Calcification; Fahr's disease; PDGFRB; SLC20A2

Indexed keywords

ADULT; ARTICLE; BRAIN CALCIFICATION; CEREBELLUM VERMIS; COGNITIVE DEFECT; COMPUTED TOMOGRAPHY SCANNER; COMPUTER ASSISTED TOMOGRAPHY; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; DIAGNOSTIC TEST ACCURACY STUDY; DIFFERENTIAL DIAGNOSIS; FAHR DISEASE; FEMALE; GENE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; IDIOPATHIC DISEASE; MAJOR CLINICAL STUDY; MALE; MENTAL DISEASE; MOTOR DYSFUNCTION; PDGFRB GENE; PHENOTYPE; PRIORITY JOURNAL; RATING SCALE; SCORING SYSTEM; SLC20A2 GENE;

EID: 84890539576     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awt255     Document Type: Article

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