Results 141 to 150 of about 115,934 (290)

Obesity Was Associated With Learning Disabilities in Children and Adolescents Living in the USA. [PDF]

Acta Paediatr
Gao H, Fu Q, Gao Q.
europepmc   +1 more source

The Evaluation Scale of Reading Disabilities in The Primary Schools in Northern Territory of Jordan from Learning Resources Room [PDF]

, 2019
Halaa Freihat, Nashaat Baioumy, Roslan Ab Rahman, Khaled Abu Sheieah   +3 more
openalex   +1 more source

Psychiatric Comorbidities and Treatment Modalities in Children With Osteogenesis Imperfecta: A Systematic Review of Mental Health

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT To evaluate the prevalence of psychiatric signs and symptoms and describe psychotherapeutic and psychopharmacological interventions among children with osteogenesis imperfecta (OI). PRISMA guidelines were followed, and the study was registered in PROSPERO (CRD42024588284). Studies (n = 1419) were identified across five databases.
Julia M. Morales, Camille F. Villar, Beatriz Varman, Gianna M. Colombo, Danqi Li, Sarah J. Sadek, Marie‐Eve Robinson, Chaya N. Murali, Kara Ayers, Jocelyn Gomez, Brendan Lee, V. Reid Sutton, Eric A. Storch, Andrew D. Wiese   +13 more
wiley   +1 more source

Association between maternal smoking during pregnancy and learning disabilities in children and adolescents: A propensity score matching analysis. [PDF]

Tob Induc Dis
Li P, Lu T, Wang W, Du L.
europepmc   +1 more source

Genetic and Phenotypic Features of the Five Known Polyaminopathies: A Critical Narrative Review

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Polyaminopathies are a recently described family of rare genetic neurodevelopmental disorders. Polyaminopathies disrupt the biosynthesis of the primary polyamines: putrescine, spermidine, and spermine. Snyder–Robinson syndrome results from hemizygous loss‐of‐function variants in the spermine synthase (SMS) gene, resulting in decreased or ...
Elizabeth A. VanSickle, Sara M. Sarasua, Tracy Lowe, Christopher L. Farrell, Luigi Boccuto, Charles Schwartz, Anthony E. Pegg, Angela Peron, Victor Faundes, Mythily Ganapathi, Wendy K. Chung, Alban Ziegler, Floris Hofstede, Clément Prouteau, Katharina Steindl, Colleen Olson, Orrin Devinsky, Teresa L. Mastracci, Robert A. Casero Jr., Tracy Murray Stewart, Susan Gilmour, Teri Koerner, Mary Jo Kutler, Surender Rajasekaran, Julianne Michael, André S. Bachmann, Caleb P. Bupp   +26 more
wiley   +1 more source

Charting the knowledge landscape of mathematics learning disabilities: an analysis of intellectual structure and research frontiers. [PDF]

Front Psychol
Li C, Wang L.
europepmc   +1 more source

A Guide to Psychological Understanding of People with Learning Disabilities: Eight Domains and Three Stories

, 2013
Jenny Webb
openalex   +1 more source

Exploring England's Palliative and End‐of‐Life Care Systems for People With Learning Disabilities: The Perspectives of Senior Health and Social Care Professionals and Commissioners [PDF]

Ned Redmore, Louise Wallace, Irene Tuffrey‐Wijne   +2 more
openalex   +1 more source

Anesthesia for Cesarean Delivery and Learning Disabilities in a Population-based Birth Cohort [PDF]

, 2009
Juraj Šprung, Randall P. Flick, Robert T. Wilder, Slavica K. Katusic, Tasha L. Pike, Mariella Dingli, Stephen J. Gleich, Darrell R. Schroeder, William J. Barbaresi, Andrew C. Hanson, David O. Warner   +10 more
openalex   +1 more source

Noonan Syndrome Spectrum Disorders Predispose to Systemic Lupus Erythematosus: Case Report and Critical Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT RASopathies are clinically overlapping neurodevelopmental syndromes resulting from germline mutations in genes involved in the rat sarcoma/mitogen‐activated protein kinases (RAS/MAPK) pathway. Historically, RASopathies have been described by clinical phenotypes, such as Noonan syndrome and Neurofibromatosis type I.
Anastasia‐Vasiliki Madenidou, Gillian I. Rice, James O'Sullivan, Ben Parker, Ian N. Bruce, Emma Burkitt‐Wright, Tracy A. Briggs   +6 more
wiley   +1 more source