Alternating hemiplegia of childhood: ATP1A3 gene analysis in 16 patients;Hemiplejía alternante de la infancia: estudio del gen ATP1A3 en 16 pacientes

Medicina Clinica

Volumn 143, Issue 1, 2014, Pages 25-28

  Ulate Campos, Adriana ^a   Fons, Carmen ^a,b   Campistol, Jaume ^a,b   Martorell, Loreto ^a,b   Cancho Candela, Ramón ^c   Eiris, Jesús ^d   López Laso, Eduardo ^e   Pineda, Mercedes ^f   Sans, Anna ^a   Velázquez, Ramón ^g  

^a HOSPITAL UNIVERSITARI DE BELLVITGE   (Spain)

^b INSTITUTO DE SALUD CARLOS III   (Spain)

^c HOSPITAL UNIVERSITARIO RÍO HORTEGA   (Spain)

^d UNIVERSITY OF SANTIAGO DE COMPOSTELA   (Spain)

^e HOSPITAL UNIVERSITARIO REINA SOFÍA   (Spain)

^f Fundacion Sant Joan de Deu   (Spain)

^g HOSPITAL INFANTIL LA PAZ   (Spain)

Author keywords

Alternating hemiplegia of childhood; ATP1A3 gen; Sodium potassium adenosine triphosphatase pump

Indexed keywords

ALTERNATING HEMIPLEGIA IN CHILDHOOD; ARTICLE; ATP1A3 GENE; CHILD; CHILDHOOD DISEASE; CLINICAL ARTICLE; DIAGNOSTIC PROCEDURE; GENE; GENE IDENTIFICATION; GENE MUTATION; GENETIC ANALYSIS; HEMIPLEGIA; HUMAN; MULTICENTER STUDY; ADOLESCENT; ADULT; CLINICAL TRIAL; DIET THERAPY; DYSTONIC DISORDER; EYE MOVEMENT DISORDER; FEMALE; GENETICS; HETEROZYGOTE; KETOGENIC DIET; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; ONSET AGE; PHYSIOLOGY; POINT MUTATION; PRESCHOOL CHILD; RETROSPECTIVE STUDY; SPAIN; YOUNG ADULT;

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ATP1A3 PROTEIN, HUMAN; GLUTAMATE TRANSPORTER; SLC1A2 PROTEIN, HUMAN;

ADOLESCENT; ADULT; AGE OF ONSET; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; DYSTONIC DISORDERS; FEMALE; GLUTAMATE PLASMA MEMBRANE TRANSPORT PROTEINS; HEMIPLEGIA; HETEROZYGOTE; HUMANS; KETOGENIC DIET; MALE; MUTATION, MISSENSE; OCULAR MOTILITY DISORDERS; POINT MUTATION; RETROSPECTIVE STUDIES; SODIUM-POTASSIUM-EXCHANGING ATPASE; SPAIN; YOUNG ADULT;

EID: 84902438837     PISSN: 00257753     EISSN: 15788989     Source Type: Journal    
DOI: 10.1016/j.medcli.2014.01.036     Document Type: Article

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