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2000, Clinics in developmental medicine, ISBN 1898683190, Volume no.150, xi, 217
Book
Clinical Orthopaedics and Related Research, ISSN 0009-921X, 5/2012, Volume 470, Issue 5, pp. 1294 - 1302
Journal Article
Developmental Medicine & Child Neurology, ISSN 0012-1622, 06/2013, Volume 55, Issue 6, pp. 527 - 533
Aim This study investigated the effects of a theme‐based (‘magic’) variation of the hand–arm bimanual intensive therapy programme, in two different countries,... 
INTERVENTION PROGRAMS | METAANALYSIS | RANDOMIZED-TRIAL | PEDIATRICS | CONGENITAL HEMIPLEGIA | RELIABILITY | EXPERIENCE | SCALE | CEREBRAL-PALSY | INDUCED MOVEMENT THERAPY | VALIDITY | CLINICAL NEUROLOGY | Exercise Therapy - methods | Severity of Illness Index | Age Factors | Follow-Up Studies | Humans | Male | Treatment Outcome | United Kingdom | Functional Laterality | Arm - physiopathology | Hand - physiopathology | Motivation | Hemiplegia - psychology | Adolescent | Female | Hemiplegia - rehabilitation | Surveys and Questionnaires | Israel | Hemiplegia - physiopathology | Child | Motor Skills | Pediatrics | Medical and Health Sciences | Pediatrik | independence | evaluation | named inventories | Great Britain | outcome assessment | female | hand movement | Neurologi | hemiplegia | Hand | article | Clinical Medicine | Neurology | school child | movement therapy | adolescent | functional assessment | Arm | male | child | comparative study | group dynamics | Medicin och hälsovetenskap | childhood disease | Klinisk medicin | Exercise Therapy | follow up | clinical article | skill | Questionnaires | Assisting Hand Assessment | experimental design | learning disorder | priority journal | human | questionnaires and rating scales | behavior disorder | Children Hand Experience Questionnaire | performance | controlled study | hand arm bimanual intensive therapy
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2015, Volume 52, Issue 1, pp. 56 - 64
Abstract Background ATP1A3 mutations have now been recognized in infants and children presenting with a diverse group of neurological phenotypes, including... 
Pediatrics | Neurology | CAPOS syndrome | ataxia | rapid-onset dystonia-Parkinsonism | dystonia | ATP1A3 | hemiplegia | alternating hemiplegia of childhood | sodium potassium ATPases | FLUNARIZINE | CEREBRAL EDEMA | ALPHA-3 | MIGRAINE | CLINICAL NEUROLOGY | NA/K-ATPASE | DE-NOVO MUTATIONS | CLINICAL-MANIFESTATIONS | GENE | PEDIATRICS | CALCIUM-CHANNEL | Sodium-Potassium-Exchanging ATPase - genetics | Humans | Foot Deformities, Congenital - genetics | Hemiplegia - therapy | Cerebellar Ataxia - physiopathology | Hemiplegia - diagnosis | Hearing Loss, Sensorineural - diagnosis | Foot Deformities, Congenital - physiopathology | Dystonic Disorders - physiopathology | Dystonic Disorders - therapy | Hemiplegia - physiopathology | Child | Optic Atrophy - diagnosis | Optic Atrophy - genetics | Diagnosis, Differential | Dystonic Disorders - genetics | Optic Atrophy - physiopathology | Foot Deformities, Congenital - diagnosis | Foot Deformities, Congenital - therapy | Hearing Loss, Sensorineural - genetics | Reflex, Abnormal - genetics | Optic Atrophy - therapy | Phenotype | Animals | Cerebellar Ataxia - genetics | Cerebellar Ataxia - therapy | Dystonic Disorders - diagnosis | Hearing Loss, Sensorineural - therapy | Hemiplegia - genetics | Mutation | Cerebellar Ataxia - diagnosis | Hearing Loss, Sensorineural - physiopathology | Hemiplegia | Genetic aspects | Parkinson's disease | Dystonia
Journal Article