Results 171 to 180 of about 8,409,709 (279)

Other title: Client Assessment Referral and Evaluation Level II Instruction Manual : Intellectual Disability/Developmental Disability/Related Conditions Other title: Level II Instruction Manual : Intellectual Disability/Developmental Disability/Related Conditions; Other title: Intellectual Disability/Developmental Disability/Related Conditions

, 2015
"Effective July 1, 2015.""Instructions For CARE Level II Preadmission Screening Intellectual/Other Developmental Disabilities/Related Conditions.
Kansas. Department for Aging and Disability Services. CARE Program.
core  

Localizing value of ecstatic phenomenon in epilepsy surgery: A systematic review

Epileptic Disorders, EarlyView.
Abstract Objective A systematic review was conducted to synthesize current anatomo‐clinical correlations of ecstatic symptoms in focal epilepsy, aiming to provide evidence‐based guidance for interpreting this ictal semiology during presurgical evaluation.
Mihai Dragos Maliia, Fabrice Bartolomei, Fabienne Picard   +2 more
wiley   +1 more source

The X-Linked Intellectual Disability Gene, ZDHHC9 , Is Important for Oligodendrocyte Subtype Determination and Myelination. [PDF]

Glia
White RB, Wild AR, O'Leary TP, Thompson AJ, Flibotte S, Peng A, Rogalski JC, Mair M, Derhami N, Bamji SX.   +9 more
europepmc   +1 more source

Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X-linked intellectual disability

, 2023
Kim C, Lee Y, Thomas M, Roychaudhury A, Skinner C, Maconachie G, Crosier M, Horak H, Constantinescu C, Choi T, Kyung J, Wang T, Ku B, Chodirker B, Hammer M, Gottlob I, Norton W, Chudley A, Schwartz C.   +18 more
europepmc   +1 more source

X-linked intellectual disability-plagiocephaly syndrome [PDF]

, 2020
openaire   +1 more source

Epilepsy‐associated SCN2A‐L1342P mutation drives network hyperexcitability and widespread transcriptomic changes in human cortical organoids

Epilepsia, EarlyView.
Abstract Objective SCN2A pathogenic mutations, such as the recurrent heterozygous Nav1.2‐L1342P, are monogenic causes of epilepsy. In this human‐induced pluripotent stem cell–derived model system, we aim to investigate the molecular and cellular mechanisms underlying SCN2A‐L1342P‐associated pathology. Methods Using a human male induced pluripotent stem
Maria I. Olivero‐Acosta, Morgan Robinson, Zhefu Que, Zaiyang Zhang, Karen V. Salazar‐Salazar, Hope Elizabeth Harlow, Vinayak Shankar, Seoyeon Hong, Muhan Wang, Conrad M. Otterbacher, Hina Kadono, Manasi Halurkar, Harish Kothandaraman, Nadia Atallah Lanman, Trang Nguyen, Kyle Wettschurack, Benjamin Zirkle, Layan Yunis, Ningren Cui, Xiaoling Chen, Jingliang Zhang, Jiaxiang Wu, William C. Skarnes, Chongli Yuan, Feng Guo, Megan Abbott, Yang Yang   +26 more
wiley   +1 more source

A New Family with X-Linked Intellectual Disability 90: A Case Report of a <i>Novel DLG3</i> Variant and Literature Review. [PDF]

Mol Syndromol
Alavanda C, Çıkı K.
europepmc   +1 more source

Exon 21 deletion in the OPHN1 gene in a family with syndromic X-linked intellectual disability: Case report. [PDF]

Medicine (Baltimore), 2020
Bogliş A, Cosma AS, Tripon F, Bãnescu C.   +3 more
europepmc   +1 more source

X-linked intellectual disability, Nascimento type [PDF]

, 2020
openaire   +1 more source

Enhancing quality of mental health service for veterans with seizures

Epilepsia, EarlyView.
Abstract Psychiatric disorders are commonly identified in people with seizures (PWS). Comorbid mood, anxiety, and trauma‐ and stressor‐related disorders are highly prevalent and not consistently recognized or treated promptly. Veterans with seizures are particularly vulnerable to neuropsychiatric comorbidities, including a higher prevalence of ...
Maria Raquel Lopez, W. Curt LaFrance Jr., Kristen Mordecai, Anna E. Blanken, Mary Jo Pugh, Krista Ocier, Hamada Altalib   +6 more
wiley   +1 more source