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Academic Journal

The Healthcare and Societal Costs of Familial Intellectual Disability.

Subjects: Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/epidemiology ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/genetics; Humans

  • Source: International journal of environmental research and public health [Int J Environ Res Public Health] 2024 Mar 04; Vol. 21 (3). Date of Electronic Publication: 2024 Mar 04.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101238455 Publication Model: Electronic Cited Medium: Internet ISSN: 1660-4601

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Academic Journal

A novel variant in ASNS gene responsible for syndromic intellectual disability and microcephaly: Case report and literature review.

  • Authors : Jahanpanah M; Department of Genetics and Pathology, Ardabil University of Medical Sciences, Ardabil, Iran.; Mokhtari D

Subjects: Microcephaly*/Microcephaly*/Microcephaly*/genetics ; Microcephaly*/Microcephaly*/Microcephaly*/diagnosis ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/genetics

  • Source: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Apr; Vol. 12 (4), pp. e2424.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

A severe neurocognitive phenotype caused by biallelic CHD3 variants in two siblings.

Subjects: Siblings* ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/diagnosis ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/genetics Snijders Blok-Campeau syndrome

  • Source: American journal of medical genetics. Part A [Am J Med Genet A] 2024 Apr; Vol. 194 (4), pp. e63503. Date of Electronic Publication: 2023 Dec 20.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Report

A novel variant in CYFIP2 in a girl with severe disabilities and bilateral perisylvian polymicrogyria.

  • Authors : Salokivi T; Department of Disability Services, The Wellbeing Services County of Southwest Finland, Paimio, Finland.; Parkkola R

Subjects: Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/genetics ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/complications ; Polymicrogyria*/Polymicrogyria*/Polymicrogyria*/genetics Perisylvian syndrome

  • Source: American journal of medical genetics. Part A [Am J Med Genet A] 2024 Apr; Vol. 194 (4), pp. e63478. Date of Electronic Publication: 2023 Nov 17.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Genetic determinants of global developmental delay and intellectual disability in Ukrainian children.

  • Authors : Shchubelka K; Department of Biological Sciences, Oakland University, 118 Library Drive, Rochester, Yaroslava Hasynets, MI, 48309, USA.; Department of Biology, State University 'Uzhhorod National University', Voloshyna street, 32, Uzhhorod, 88000, Ukraine.

Subjects: Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/epidemiology ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/genetics ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/diagnosis

  • Source: Journal of neurodevelopmental disorders [J Neurodev Disord] 2024 Mar 27; Vol. 16 (1), pp. 13. Date of Electronic Publication: 2024 Mar 27.Publisher: BioMed Central Country of Publication: England NLM ID: 101483832 Publication Model: Electronic Cited Medium: Internet ISSN: 1866-1955

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Academic Journal

De novo variants in DENND5B cause a neurodevelopmental disorder.

Subjects: Neurodevelopmental Disorders*/Neurodevelopmental Disorders*/Neurodevelopmental Disorders*/genetics ; Neurodevelopmental Disorders*/Neurodevelopmental Disorders*/Neurodevelopmental Disorders*/metabolism ; Epilepsy*/Epilepsy*/Epilepsy*/genetics

  • Source: American journal of human genetics [Am J Hum Genet] 2024 Mar 07; Vol. 111 (3), pp. 529-543. Date of Electronic Publication: 2024 Feb 21.Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Molecular and phenotypical findings of a novel de novo SYNGAP1 gene variant in an 11-year-old Iranian boy with intellectual disability.

  • Authors : Mir A; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.; Song Y

Subjects: Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/diagnosis ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/genetics ; ras GTPase-Activating Proteins*/ras GTPase-Activating Proteins*/ras GTPase-Activating Proteins*/genetics

  • Source: Laboratory medicine [Lab Med] 2024 Mar 07; Vol. 55 (2), pp. 204-208.Publisher: Oxford University Press Country of Publication: England NLM ID: 0250641 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Racial and ethnic disparities in the co-occurrence of intellectual disability and autism: Impact of incorporating measures of adaptive functioning.

  • Authors : Furnier SM; Department of Population Health Sciences, University of Wisconsin-Madison, Madison, Wisconsin, USA.; Waisman Center, University of Wisconsin-Madison, Madison, Wisconsin, USA.

Subjects: Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/complications ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/epidemiology ; Autistic Disorder*/Autistic Disorder*/Autistic Disorder*/complications

  • Source: Autism research : official journal of the International Society for Autism Research [Autism Res] 2024 Mar; Vol. 17 (3), pp. 650-667. Date of Electronic Publication: 2024 Feb 28.Publisher: John Wiley & Sons, Inc Country of Publication: United States NLM ID: 101461858 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Diagnostic Overshadowing of Psychological Disorders in People With Intellectual Disability: A Systematic Review.

  • Authors : Dell'Armo K; Kristin Dell'Armo, Nationwide Children's Hospital and The Ohio State University.; Tassé MJ

Subjects: Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/diagnosis ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/psychology ; Problem Behavior*

  • Source: American journal on intellectual and developmental disabilities [Am J Intellect Dev Disabil] 2024 Mar 01; Vol. 129 (2), pp. 116-134.Publisher: American Association on Intellectual and Developmental Disabilities Country of Publication: United States NLM ID: 101492916

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Academic Journal

Effectiveness of music therapy in enhancing empathy and emotional recognition in adolescents with intellectual disabilities.

  • Authors : Huang C; General Education and International College, Chongqing College of Electronic Engineering, Chongqing, China. Electronic address: .; Gu S

Subjects: Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/therapy ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/psychology ; Music Therapy*

  • Source: Acta psychologica [Acta Psychol (Amst)] 2024 Mar; Vol. 243, pp. 104152. Date of Electronic Publication: 2024 Jan 19.Publisher: North Holland Publishing Country of Publication: Netherlands NLM ID: 0370366 Publication Model: Print-Electronic Cited Medium: Internet

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  • 1-10 of  70,697 results for ""Intellectual Disability""