Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Dongnhu T, Truong"'
Autor:
Abolfazl Doostparast Torshizi, Dongnhu T. Truong, Liping Hou, Bart Smets, Christopher D. Whelan, Shuwei Li
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-16 (2024)
Abstract Parkinson’s disease is highly heterogeneous across disease symptoms, clinical manifestations and progression trajectories, hampering the identification of therapeutic targets. Despite knowledge gleaned from genetics analysis, dysregulated
Externí odkaz:
https://doaj.org/article/af48a3f67403494c92d6384ce4e6936d
Autor:
Lisa A. Gabel, Alexandria Battison, Dongnhu T. Truong, Esther R. Lindström, Kelsey Voss, Yih-Choung Yu, Sorawit Roongruengratanakul, Khaknazar Shyntassov, Samantha Riebesell, Nicole Toumanios, Christiana M. Nielsen-Pheiffer, Steven Paniagua, Jeffrey R. Gruen
Publikováno v:
Dev Neurosci
Reading disability (RD), which affects between 5 and 17% of the population worldwide, is the most prevalent form of learning disability, and is associated with underactivation of a universal reading network in children. However, recent research sugge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ede71d36968ee5d5e9c82d1bec46c383
https://doi.org/10.1159/000527480
https://doi.org/10.1159/000527480
Autor:
Steven Paniagua, Dongnhu T. Truong, Erin M. Murray, Lisa A. Gabel, Karla Cariño, Evelyn S. Johnson, Jeffrey R. Gruen, Esther R. Lindström, Christiana M. Nielsen, Kelsey Voss
Publikováno v:
Developmental Neuroscience. 43:116-133
Dyslexia is a common learning disability that affects processing of written language despite adequate intelligence and educational background. If learning disabilities remain untreated, a child may experience long-term social and emotional problems,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4876922dfb962a8c7c90784119691b17
https://doi.org/10.1159/000516667
https://doi.org/10.1159/000516667
Autor:
Julio Molineros, Katherine Elliott, Dongnhu T Truong, Hai Fang, Amy Hart, Shuwei Li, Dawn Waterworth, Julian C Knight, Mary Helen Black
Publikováno v:
The Journal of Immunology. 208:160.02-160.02
Prevalence of immune mediated disease (IMD) within N. European populations varies from common (atopic dermatitis AD=10%) to rarer (giant cell arteritis-GCA=0.02%; hidradenitis suppurativa-HS=0.77%). This directly affects statistical power to detect g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc7aa348a9ea6609d7dbb817bac34ff4
https://doi.org/10.4049/jimmunol.208.supp.160.02
https://doi.org/10.4049/jimmunol.208.supp.160.02
Autor:
Dongnhu T Truong, Julio Molineros, Yanqing Chen, Meijian Guan, Amy Hart, Bryce Keyes, Karsten B. Seiber, Shuwei Li, Dawn Waterworth, Mary Helen Black
Publikováno v:
The Journal of Immunology. 208:60.03-60.03
Background Dupilumab is the only approved biologic used to treat moderate to severe atopic dermatitis (AD) but has a non-response rate of 55–60%. This suggests underlying heterogeneity in AD etiology, requiring alternate therapies for patients. Stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::468e931420e1fed8f18bcce1489b31e2
https://doi.org/10.4049/jimmunol.208.supp.60.03
https://doi.org/10.4049/jimmunol.208.supp.60.03
Publikováno v:
PLoS ONE, Vol 8, Iss 9, p e73144 (2013)
Disruption of neuronal migration in humans is associated with a wide range of behavioral and cognitive outcomes including severe intellectual disability, language impairment, and social dysfunction. Furthermore, malformations of cortical development
Externí odkaz:
https://doaj.org/article/f1f564c2abb348e99ae281113b3a9f61
Akademický článek
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Autor:
Andrew K. Adams, Richard K. Olson, Bruce F. Pennington, Dongnhu T. Truong, Shelley D. Smith, Erik G. Willcutt, Jeffrey R. Gruen, John C. DeFries
Publikováno v:
Human Genetics
Eleven loci with prior evidence for association with reading and language phenotypes were sequenced in 96 unrelated subjects with significant impairment in reading performance drawn from the Colorado Learning Disability Research Center collection. Ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c9170dcbf527a217e5585836a1188bc
https://doi.org/10.1007/s00439-017-1838-z
https://doi.org/10.1007/s00439-017-1838-z
Autor:
Jeffrey R. Gruen, Mellissa M C DeMille, Jan C. Frijters, Joan Bosson-Heenan, Miao Li, Maureen W. Lovett, Jeffrey G. Malins, Dongnhu T. Truong
Publikováno v:
Child Neuropsychol
Recent studies of co-occurring reading disorder (RD) and attention deficit/hyperactivity disorder (ADHD), and co-occurring RD and language impairment (LI), support a core disability plus co-occurrence model focused on language and attention. Genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::417f1bb53ebf12984c1e0e17fd0c4b12
https://pubmed.ncbi.nlm.nih.gov/31411106
https://pubmed.ncbi.nlm.nih.gov/31411106
Autor:
Richard Boada, Andrew K. Adams, Maryanne Wolf, Jan C. Frijters, Jeffrey R. Gruen, John C. DeFries, Simon E. Fisher, Clyde Francks, Bruce F. Pennington, Dongnhu T. Truong, Shelley D. Smith, Joan Bosson-Heenan, E. Mark Mahone, Dina E. Hill, Richard K. Olson, Maureen W. Lovett, Steven Paniagua, Alessandro Gialluisi, Erik G. Willcutt
Publikováno v:
Journal of Medical Genetics
Journal of Medical Genetics, 56, 557-566
Journal of Medical Genetics, 56, 8, pp. 557-566
Journal of Medical Genetics, 56, 557-566
Journal of Medical Genetics, 56, 8, pp. 557-566
BackgroundRapid automatised naming (RAN) and rapid alternating stimulus (RAS) are reliable predictors of reading disability. The underlying biology of reading disability is poorly understood. However, the high correlation among RAN, RAS and reading c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::166df76a7cc465784b33c841ce197116
https://doi.org/10.1136/jmedgenet-2018-105874
https://doi.org/10.1136/jmedgenet-2018-105874
