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How Andrew Yang's Personal Experience With Autism Is Shaping His Policy Proposals

• Source: All Things Considered. January 2, 2020

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Agricola

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Education Full Text (H.W. Wilson)

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Education Full Text (H.W. Wilson)

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GABAergic/Glycinergic and Glutamatergic Neurons Mediate Distinct Neurodevelopmental Phenotypes of STXBP1 Encephalopathy.

• Authors : Joo Hyun Kim; Wu Chen; Chao, Eugene S.

Subjects: BRAIN diseases; SYNAPTIC vesicles; NEURONS

• Source: Journal of Neuroscience; 4/3/2024, Vol. 44 Issue 14, p1-19, 19p

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The gut metabolite indole-3-propionic acid activates ERK1 to restore social function and hippocampal inhibitory synaptic transmission in a 16p11.2 microdeletion mouse model.

• Authors : Jiang, Jian; Wang, Dilong; Jiang, Youheng

Subjects: GUT microbiome; SOCIAL skills; NEURAL transmission

• Source: Microbiome; 3/28/2024, Vol. 12 Issue 1, p1-22, 22p

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POGZ truncating alleles cause syndromic intellectual disability

• Authors : White, Janson; Beck, Christine R.; Harel, Tamar

• Source: Genome Medicine. January 6, 2016, Vol. 8 Issue 3

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Specific brain imaging alterations underlying autistic traits in children with attention-deficit/hyperactivity disorder.

• Authors : Liu, Juan; Liu, Qian-Rong; Wu, Zhao-Min

• Source: Behavioral and Brain Functions. November 20, 2023, Vol. 19 Issue 1.

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The Associations Between Accelerometer-Measured Physical Activity Levels and Mental Health in Children and Adolescents with Intellectual Disabilities During the COVID-19 Pandemic.

• Authors : Yang W; Department of Sports Science and Physical Education, The Chinese University of Hong Kong, Hong Kong SAR, China.; Li MH

Subjects: Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/epidemiology ; COVID-19* ; Autism Spectrum Disorder*

• Source: Journal of autism and developmental disorders [J Autism Dev Disord] 2023 Dec; Vol. 53 (12), pp. 4809-4821. Date of Electronic Publication: 2022 Oct 01.Publisher: Springer Country of Publication: United States NLM ID: 7904301 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Clinical features of patients with Yin Yang 1 deficiency causing Gabriele-de Vries syndrome: A new case and review of the literature.

• Authors : Khamirani HJ; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran.; Comprehensive Medical Genetic Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Subjects: Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/genetics ; Yin-Yang*; Child

• Source: Annals of human genetics [Ann Hum Genet] 2022 Jan; Vol. 86 (1), pp. 52-62. Date of Electronic Publication: 2021 Nov 03.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0416661 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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