Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nicole, Baumer"'
Autor:
Cara Soccorso, Margaret Hojlo, Katherine Pawlowski, Angela Lombardo, Emily Davidson, Sabrina Sargado, Rafael DePillis, Nicole Baumer
Publikováno v:
Frontiers in Psychology, Vol 15 (2024)
BackgroundPrior research has characterized neurodevelopmental phenotypes for Down syndrome (DS), but there is variability in age of milestone attainment and limited identification of early predictors of developmental trajectories. Additionally, less
Externí odkaz:
https://doaj.org/article/f51998636aac422193e111c96dd07f58
Autor:
Jacob Levman, Bernadette McCann, Nicole Baumer, Melanie Y. Lam, Tadashi Shiohama, Liam Cogger, Allissa MacDonald, Emi Takahashi
Publikováno v:
Biology, Vol 13, Iss 8, p 575 (2024)
Down syndrome (DS) is a genetic disorder characterized by intellectual disability whose etiology includes an additional partial or full copy of chromosome 21. Brain surface morphometry analyses can potentially assist in providing a better understandi
Externí odkaz:
https://doaj.org/article/758d4330f4db4fea918d60595eb33142
Autor:
Emi Takahashi, Nina Allan, Rafael Peres, Alpen Ortug, Andre J. W. van der Kouwe, Briana Valli, Elizabeth Ethier, Jacob Levman, Nicole Baumer, Keita Tsujimura, Nauru Idalia Vargas-Maya, Trevor A. McCracken, Rosa Lee, Alika K. Maunakea
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2023)
IntroductionAutism Spectrum Disorder (ASD) is a neurodevelopmental disorder characterized by deficits in social interaction, communication and repetitive, restrictive behaviors, features supported by cortical activity. Given the importance of the sub
Externí odkaz:
https://doaj.org/article/aa3b78fd3832434c8d3830acc64912aa
Autor:
Cara Soccorso, Anna Milliken, Margaret Hojlo, Katherine Pawlowski, Sarah Weas, Georgios Sideridis, Nicole Baumer
Publikováno v:
Journal of Developmental & Behavioral Pediatrics. 44:e185-e195
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87afc8535aabfa6dd4c32e1b986c3fb5
https://doi.org/10.1097/dbp.0000000000001171
https://doi.org/10.1097/dbp.0000000000001171
Autor:
Bernadette McCann, Jacob Levman, Nicole Baumer, Melanie Y. Lam, Tadashi Shiohama, Liam Cogger, Allissa MacDonald, Prahar Ijner, Emi Takahashi
Publikováno v:
NeuroImage: Clinical, Vol 32, Iss , Pp 102815- (2021)
Down syndrome (DS) is a genetic disorder caused by the presence of an extra full or partial copy of chromosome 21 and characterized by intellectual disability. We hypothesize that performing a retrospective analysis of 73 magnetic resonance imaging (
Externí odkaz:
https://doaj.org/article/9d2cc63d20d3401ab8528ec6b4bae1ce
Autor:
Jacob Levman, Allissa MacDonald, Nicole Baumer, Patrick MacDonald, Natalie Stewart, Ashley Lim, Liam Cogger, Tadashi Shiohama, Emi Takahashi
Publikováno v:
NeuroImage: Clinical, Vol 23, Iss , Pp - (2019)
Down syndrome (DS) is a genetic disorder caused by an extra copy of all or part of chromosome 21 and is characterized by intellectual disability. We performed a retrospective analysis of 47 magnetic resonance imaging (MRI) examinations of participant
Externí odkaz:
https://doaj.org/article/df8fccc08d834c5ebea7cbfd7741de0d
Autor:
Jenifer, Lavigne, Christianne, Sharr, Al, Ozonoff, Lisa Albers, Prock, Nicole, Baumer, Campbell, Brasington, Sheila, Cannon, Blythe, Crissman, Emily, Davidson, Jose C, Florez, Priya, Kishnani, Angela, Lombardo, Jordan, Lyerly, Jessica B, McCannon, Mary Ellen, McDonough, Alison, Schwartz, Kathryn L, Berrier, Susan, Sparks, Kara, Stock-Guild, Tomi L, Toler, Kishore, Vellody, Lauren, Voelz, Brian G, Skotko
Publikováno v:
American journal of medical genetics. Part A. (11)
The Down Syndrome Study Group (DSSG) was founded in 2012 as a voluntary, collaborative effort with the goal of supporting evidenced-based health care guidelines for individuals with Down syndrome (DS). Since then, 5 DS specialty clinics have collecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0f61c517b33c95cfe3f6856482679fcd
https://pubmed.ncbi.nlm.nih.gov/26249752
https://pubmed.ncbi.nlm.nih.gov/26249752