Results 81 to 90 of about 1,251,558 (233)
The Early Diagnosis of Preschool Children with Autism Spectrum Disorder in Norway: a Study of Diagnostic Age and Its Associated Factors [PDF]
Scandinavian Journal of Child and Adolescent Psychiatry and Psychology, 2015 Kenneth Larsen
doaj +1 more source
Tourette syndrome research highlights from 2019 [version 2; peer review: 2 approved]
F1000Research, 2020 This is the sixth yearly article in the Tourette Syndrome Research Highlights series, summarizing research from 2019 relevant to Tourette syndrome and other tic disorders.
Andreas Hartmann +2 more
doaj +1 more source
Descrição atualizada da paralisia cerebral
Developmental Medicine &Child Neurology, EarlyView.Resumo A paralisia cerebral (PC) é um termo descritivo amplamente utilizado para um espectro de deficiências motoras causadas por lesão ou malformação cerebral não progressiva ocorrida durante as fases iniciais do desenvolvimento. Avanços recentes nas áreas da genética, de pesquisa em inflamação e em neurofisiologia têm refinado a compreensão ...
Bernard Dan +5 more
wiley +1 more source
At a glance : Tourette Syndrome [PDF]
CDC is committed to:\ue2\u20ac\ua2 Increasing our understand of Tourette syndrome,\ue2\u20ac\ua2 Educating communities, families, educators and providers about TS,\ue2\u20ac\ua2 And helping improve the lives of people with TS.tourette-overview-fact-sheet-
core
Neurobiology of Tourette syndrome
Biological Psychiatry, 1995 This article includes a discussion of approaches designed to determine neuroanatomic localization through the use of physical examination, electrophysiologic and neuroradiographic studies, and neuropathologic evaluations. The author reviews the anatomy, function, and biochemistry of frontal-subcortical circuits.
openaire +2 more sources
Developmental Medicine &Child Neurology, EarlyView.Aim To determine the interrater reliability and stability of the Gross Motor Function Classification System (GMFCS), Manual Ability Classification System (MACS)/Mini‐MACS, and Communication Function Classification System (CFCS) in individuals with STXBP1‐ and SYNGAP1‐related disorders.
Samuel R. Pierce +6 more
wiley +1 more source
Sleep profiles in individuals with rare neurogenetic syndromes
Developmental Medicine &Child Neurology, EarlyView.Aim To characterize sleep profiles in individuals with neurogenetic disorders (NGDs) and examine the contribution of key clinical and psychiatric symptoms to these profiles. Method The parents of 248 individuals (aged 3–45 years) diagnosed with a range of NGDs, including PTEN hamartoma tumor syndrome (n = 111), SYNGAP1‐related intellectual disability ...
Isabella C. Reyes +7 more
wiley +1 more source
Developmental Medicine &Child Neurology, EarlyView.Abstract Aim To identify the outcomes reported in published studies of intervention approaches used with non‐degenerative childhood hyperkinetic movement disorders, including dystonia, dyskinesia, hypertonia, athetosis, chorea, cerebral palsy, involuntary movement, and kernicterus, and map them to the International Classification of Functioning ...
Hortensia Gimeno +10 more
wiley +1 more source
Jornal de Pediatria, 2004 OBJETIVO: Revisar as teorias e evidências das bases neurobiológicas do transtorno obsessivo-compulsivo e da síndrome de Tourette. FONTES DOS DADOS: Revisão dos estudos que investigam a neuroanatomia, neuroimagem, genética e imunologia desses transtornos.
Marcos T. Mercadante +3 more
doaj +1 more source
THE GENETICS OF TOURETTE SYNDROME
Neurologic Clinics, 1997 Tourette syndrome has significant genetic determinants. The mode of transmission, while mildly controversial, generally is thought to be due to a single major locus inherited either as an autosomal dominant trait with reduced penetrance, or as a trait with intermediate inheritance in which some heterozygotes manifest the disorder. These is evidence for
J P, Alsobrook, D L, Pauls
openaire +2 more sources