Raggruppamento Primario: Sindromi genetiche

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Individualized Remotely Supervised Motor Activity Programs Promote Rehabilitation Goal Achievement, Motor Functioning, and Physical Activity of People with Rett Syndrome-A Single-Cohort Study

Ligamentous laxity in children with achondroplasia: Prevalence, joint involvement, and implications for early intervention strategies

Craniopagus: a proposed nursing care protocol

Occupational Therapy Intervention in the Child with Leukodystrophy: Case Report

Evaluation of test-retest reliability and concurrent validity of the Italian version of the pediatric evaluation of disability inventory in children with down syndrome: A cross-sectional study

Visual assessment in Down Syndrome: The relevance of early visual functions

Functional assessment tools in children with Pompe disease: A pilot comparative study to identify suitable outcome measures for the standard of care

19q12q13.2 duplication syndrome: neuropsychiatric long-term follow-up of a new case and literature update

Lissencephaly: presentation of a clinical case of LIS 1 with a diagnosis confirmed by MLPA method and indications for rehabilitation treatment in childhood

Interstitial 11q deletion: genomic characterization and neuropsychiatric follow up from early infancy to adolescence and literature review

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