The expanding clinical and genetic spectrum of ATP1A3-related disorders

Neurology

Volumn 82, Issue 11, 2014, Pages 945-955

  Rosewich, Hendrik ^a   Ohlenbusch, Andreas ^a   Huppke, Peter ^a   Schlotawa, Lars ^a   Baethmann, Martina ^b   Carrilho, Inês ^c   Fiori, Simona ^d,e   Lourenço, Charles Marques ^f   Sawyer, Sarah ^g   Steinfeld, Robert ^a   Gärtner, Jutta ^a   Brockmann, Knut ^a  

^a UNIVERSITY MEDICAL CENTER GÖTTINGEN   (Germany)

^b Krankenhaus Dritter Orden   (Germany)

^c Institute of Biomedical Sciences Abel Salazar   (Portugal)

^d 4IRCCS Stella Maris ^*  (Italy)

^e UNIVERSITY OF PISA   (Italy)

^f UNIVERSITY OF SÃO PAULO   (Brazil)

^g CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ALTERNATING HEMIPLEGIA OF CHILDHOOD; ARTICLE; ATP1A3 GENE; CHEMICAL STRESS; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE COURSE; DISEASE SEVERITY; DYSTONIA; EMOTIONAL STRESS; EXON; FEMALE; GENE; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HEMIPLEGIA; HUMAN; MALE; PARKINSONISM; PHYSICAL STRESS; PRESCHOOL CHILD; PRIORITY JOURNAL; RAPID ONSET DYSTONIA PARKINSONISM; SCHOOL CHILD;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; COHORT STUDIES; DNA MUTATIONAL ANALYSIS; DYSTONIC DISORDERS; FEMALE; GENETIC ASSOCIATION STUDIES; GENOTYPE; HEMIPLEGIA; HUMANS; INFANT; MALE; META-ANALYSIS AS TOPIC; MUTATION; SODIUM-POTASSIUM-EXCHANGING ATPASE; YOUNG ADULT;

EID: 84898729032     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0000000000000212     Document Type: Article

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