Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Kyle J. Steinman"'
Autor:
Lisa V. Ibañez, Ann Vander Stoep, Kathleen Myers, Chuan Zhou, Shannon Dorsey, Kyle J. Steinman, Wendy L. Stone
Publikováno v:
BMC Psychiatry, Vol 19, Iss 1, Pp 1-13 (2019)
Abstract Background Despite the known benefits of early, specialized intervention for toddlers with Autism Spectrum Disorder (ASD), access to such intervention remains limited. This pragmatic trial examines a novel healthcare delivery model (Screen-R
Externí odkaz:
https://doaj.org/article/98af21f73aab43f8818f6ecb658b90d4
Publikováno v:
Acad Pediatr
OBJECTIVE: To determine whether an intervention addressing both logistical and knowledge barriers to early screening for autism spectrum disorder (ASD) increases evidence-based screening during 18-month well-child visits and PCPs’ perceived self-ef
Autor:
Leslie Sim, Celeste Steggall, Karen E. Weiss, Ian Kodish, Aaron D. Fobian, Sharon Yurs, Kyle J Steinman
Publikováno v:
Journal of Clinical Psychology in Medical Settings. 28:90-101
Pediatric functional neurological symptom disorder (FNSD or conversion disorder) is an often misunderstood but treatable condition that frequently presents in medical settings with unexplained symptoms. Although research regarding treatment of pediat
Autor:
Christelle Moufawad El Achkar, Alyssa Rosen, Sudha Kilaru Kessler, Kyle J. Steinman, Sarah J. Spence, Melissa Ramocki, Elysa Jill Marco, LeeAnne Green Snyder, John E. Spiro, Wendy K. Chung, Poduri Annapurna, Elliott H. Sherr
Publikováno v:
Neurology Genetics. 8:e200018
Background and ObjectivesDeletions and duplications at 16p11.2 (BP4 to BP5; 29.5–30.1 Mb) have been associated with several neurodevelopmental and neuropsychiatric disorders including autism spectrum disorder, intellectual disability (ID), and schi
Autor:
Wendy K. Chung, Ellen Hanson, Raphael Bernier, Robin P. Goin-Kochel, Catherine Lord, Somer L. Bishop, Kyle J. Steinman, So Hyun Kim, LeeAnne Green-Snyder
Publikováno v:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, vol 183, iss 6
Am J Med Genet B Neuropsychiatr Genet
Am J Med Genet B Neuropsychiatr Genet
Expressive language impairment is one of the most frequently associated clinical features of 16p11.2 copy number variations (CNV). However, our understanding of the language profiles of individuals with 16p11.2 CNVs is still limited. This study build
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f35a7abe1b28d6f80a224a3cf4107fe9
https://escholarship.org/uc/item/6h67t169
https://escholarship.org/uc/item/6h67t169
Autor:
Karen E, Weiss, Kyle J, Steinman, Ian, Kodish, Leslie, Sim, Sharon, Yurs, Celeste, Steggall, Aaron D, Fobian
Publikováno v:
Journal of clinical psychology in medical settings. 28(1)
Pediatric functional neurological symptom disorder (FNSD or conversion disorder) is an often misunderstood but treatable condition that frequently presents in medical settings with unexplained symptoms. Although research regarding treatment of pediat
Autor:
Caitlin M. Hudac, Trent D. DesChamps, Jessica L. Peterson, Kyle J. Steinman, Arianne S. Wallace, Michael H. Duyzend, Raphael Bernier, Xander Nuttle, Evan E. Eichler
Publikováno v:
Clinical Case Reports
Key Clinical Message 16p11.2 deletions and duplications are commonly associated with autism spectrum disorder and linked to mirrored phenotypes of physical characteristics and higher penetrance for deletions. A male with a rare 16p11.2 triplication d
Autor:
Kyle J. Steinman, Shannon Dorsey, Kathleen Myers, Lisa V. Ibañez, Chuan Zhou, Ann Vander Stoep, Wendy L. Stone
Publikováno v:
BMC Psychiatry
BMC Psychiatry, Vol 19, Iss 1, Pp 1-13 (2019)
BMC Psychiatry, Vol 19, Iss 1, Pp 1-13 (2019)
Background Despite the known benefits of early, specialized intervention for toddlers with Autism Spectrum Disorder (ASD), access to such intervention remains limited. This pragmatic trial examines a novel healthcare delivery model (Screen-Refer-Trea
Autor:
Elliott H. Sherr, Monica Proud, Qixuan Chen, Sarah J. Spence, Wendy K. Chung, Elysa J. Marco, Sudha Kilaru Kessler, LeeAnne Green Snyder, Kyle J. Steinman, Debra D'Angelo, Melissa B. Ramocki
Publikováno v:
American Journal of Medical Genetics Part A. 170:2943-2955
Chromosome 16p11.2 deletions and duplications are among the most frequent genetic etiologies of autism spectrum disorder (ASD) and other neurodevelopmental disorders, but detailed descriptions of their neurologic phenotypes have not yet been complete
Autor:
Kyle J. Steinman, Donald L. Chi, Scott D. Lindgren, Elizabeth T. Momany, Lloyd Mancl, Samuel H. Zinner
Publikováno v:
American Journal of Preventive Medicine. 50:609-615
Introduction Medicaid-enrolled children with autism spectrum disorder (ASD) encounter significant barriers to dental care. Iowa's I-Smile Program was implemented in 2006 to improve dental use for all children in Medicaid. This study compared dental h