The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene

Brain

Volumn 130, Issue 3, 2007, Pages 828-835

  Brashear, Allison ^a   Dobyns, William B ^b   De Carvalho Aguiar, Patricia ^c,g   Borg, Michel ^h   Frijns, C J M ⁱ   Gollamudi, Seema ^c   Green, Andrew ^k   Guimaraes, João ^m   Haake, Bret C ^e   Klein, Christine ⁿ   Linazasoro, Gurutz ^p   Münchau, Alexander ^o   Raymond, Deborah ^d   Riley, David ^f   Saunders Pullman, Rachel ^d   Tijssen, Marina A J ^j   Webb, David ^l   Zaremba, Jacek ^q   Bressman, Susan B ^d   Ozelius, Laurie J ^c  

^a WAKE FOREST SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF CHICAGO   (United States)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^d BETH ISRAEL MEDICAL CENTER   (United States)

^e Meritcare Health System   (United States)

^f UNIVERSITY HOSPITALS OF CLEVELAND   (United States)

^g HOSPITAL ISRAELITA ALBERT EINSTEIN   (Brazil)

^h UNIVERSITÉ CÔTE D'AZUR   (France)

ⁱ UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^j UNIVERSITY OF AMSTERDAM   (Netherlands)

^k OUR LADY S CHILDREN S HOSPITAL   (Ireland)

^l Our Lady's Hospital for Sick Children   (United Kingdom)

^m UNIVERSIDADE NOVA DE LISBOA   (Portugal)

ⁿ UNIVERSITY OF LÜBECK   (Germany)

^o UNIVERSITY OF HAMBURG   (Germany)

^p Centro de Investigacion Parkinson   (Spain)

^q INSTITUTE OF PSYCHIATRY AND NEUROLOGY   (Poland)

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Author keywords

ATP1A3; Dystonia; Na+ K+ ATPase; Parkinsonism; Rapid onset dystonia parkinsonism; RDP

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM) ALPHA 3; UNCLASSIFIED DRUG;

ACUTE DISEASE; ARTICLE; BRAIN REGION; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DYSTONIA; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENOTYPE; HETEROZYGOTE; HUMAN; LIMB PAIN; PARKINSONISM; PHENOTYPE; PRIORITY JOURNAL; RAPID ONSET DYSTONIA PARKINSONISM; TREMOR;

ADOLESCENT; ADULT; AGE OF ONSET; CHILD; CHILD, PRESCHOOL; DYSTONIA; EXTREMITIES; FAMILY HEALTH; FEMALE; GENOTYPE; HETEROZYGOTE; HUMANS; MIDDLE AGED; MOVEMENT DISORDERS; MUTATION; NA(+)-K(+)-EXCHANGING ATPASE; PARKINSONIAN DISORDERS; PHENOTYPE; TREMOR;

EID: 33947131242     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awl340     Document Type: Article

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