Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Emily Stapleton"'
Publikováno v:
Frontiers in Psychology, Vol 15 (2024)
IntroductionThe development of identity formation occurs during adolescence through experiences, ideals and principle. With greater accessibility to sports, recent trends have shown increased rates of sports specialization over the past decade in you
Externí odkaz:
https://doaj.org/article/d3185a3a8aa445c0a1179f58f6fd3ae7
Autor:
James McGinley, Emily Stapleton, Emily Gale, Hannah Worrall, Caroline Podvin, Henry B. Ellis, Philip L. Wilson, Sophia Ulman
Publikováno v:
Frontiers in Psychology, Vol 14 (2024)
IntroductionWhile youth sports benefits the developing athlete, athletes may also be subject to injury and subsequent return-to-sport protocols. The current return-to-sport criteria emphasize physical measures; however, psychological measures may als
Externí odkaz:
https://doaj.org/article/1647cc3790e9470a85f8d87b74ae71b2
Autor:
James McGinley, Emily Stapleton, Hannah Worrall, Henry B. Ellis, Philip L. Wilson, Sophia Ulman
Publikováno v:
Frontiers in Psychology, Vol 13 (2022)
Athletic identity, or the degree with which individuals identify with the athlete role, is an important rehabilitation factor for sports care providers to consider; however, it lacks extensive study in youth. The purpose of this study was to identify
Externí odkaz:
https://doaj.org/article/8e660e6c00684ab7855050ab69c31b74
Autor:
Emily Stapleton, Nathan L. Goodey, Takashi Taniguchi, Andrew Davies, Alex Summerfield, Christopher J. Mellor, Peter H. Beton, Kenji Watanabe, C. Thomas Foxon, Laurence Eaves, James Wrigley, Andrei N. Khlobystov, J.D. Albar, Sergei V. Novikov, James C. Thomas, Vladimir V. Korolkov, Tin S. Cheng
Publikováno v:
Nano Letters. 18:498-504
Lattice-matched graphene on hexagonal boron nitride is expected to lead to the formation of a band-gap but requires the formation of highly strained material and has not hitherto been realised. We demonstrate that aligned, lattice-matched graphene ca
Autor:
Patrick Lawson, Chris Cappello, Carole A. Samango-Sprouse, Emily Stapleton, Sophie van Rijn, Leo M. J. de Sonneville, Teresa Sadeghin, Selena Chea
Publikováno v:
American Journal of Medical Genetics
American Journal of Medical Genetics, 176(4), 877-885
American Journal of Medical Genetics, 176(4), 877-885
47,XXY (KS) occurs in 1:650 male births, though less than 25% are ever identified. We assessed stability of neurocognitive features across diverse populations and quantified factors mediating outcome. Forty‐four boys from the Netherlands (NL) and 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7764294b41e6211b31a501496696a1e9
https://hdl.handle.net/1887/74289
https://hdl.handle.net/1887/74289
Autor:
Andrea L. Gropman, Emily Stapleton, Carole A. Samango-Sprouse, Teresa Sadeghin, Francie L. Mitchell, Thomas P. Donahue
Publikováno v:
American Journal of Medical Genetics Part A. 164:1464-1469
The aim of the study was to examine the impact of familial learning disabilities (FLD) on the phenotypic profile of 47, XXY (Klinefelter syndrome) males and the possibility that 47, XXY males with more severe cognitive deficits may be partially a con
Autor:
Carole A. Samango-Sprouse, Andrea L. Gropman, Kathryn Haskell, Robert Graw, Teresa Sadeghin, Farhad Aliabadi, Charles L Parmele, Emily Stapleton, Rebecca Vickers, Robert Jameson
Publikováno v:
Autism. 19:327-337
Studies have shown an increased head circumference and the absence of the head tilt reflex as possible risk factors for autism spectrum disorder, allowing for early detection at 12 months in typically developing population of infants. Our aim was to
Autor:
Emily Stapleton, Rick Peret, Francie L. Mitchell, Laura L. Tosi, Kathryn Haskell, Courtney Sprouse, Carole A. Samango-Sprouse, Andrea L. Gropman, Teresa Sadeghin
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 163:44-49
49, XXXXY is a rare aneuploidy and variant of Klinefelter syndrome, occurring in 1 per 80,000-100,000 live births. We present a cohort of 40 affected males, focusing on musculoskeletal problems. Subjects were participants in an annual 49er family sup
Publikováno v:
Biology of Blood and Marrow Transplantation. 24:S459
Autor:
Sherida Powell, Teresa Sadeghin, Carole A. Samango-Sprouse, Patrick Lawson, Francie L. Mitchell, Andrea L. Gropman, Emily Stapleton
Publikováno v:
American journal of medical genetics. Part C, Seminars in medical genetics. 169(2)
47, XXY occurs in up to 1 in 650 male births and is associated with androgen deficiency, neurodevelopmental delays, and atypical social-behaviors. Previously, we showed that young boys with 47, XXY who received early hormonal therapy (EHT) had signif