Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jennifer Archibald"'
Publikováno v:
Journal of dentistry for children (Chicago, Ill.). 88(2)
GAPO syndrome is a rare autosomal recessive genetic disorder, characterized by growth retardation, alopecia, pseudoanodontia, and progressive ocular changes. This disorder is caused by recessive mutations in the ANTXR1 gene and has characteristic dys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::35e1e8c8e967da89a1340b8640559f81
https://pubmed.ncbi.nlm.nih.gov/34321146
https://pubmed.ncbi.nlm.nih.gov/34321146
Autor:
Yara A. Halasa-Rappel, Michael Hong, Paulina Miller, Rosalyn Sulyanto, Jennifer Archibald, Man Wai Ng, R. Frederick Lambert
Publikováno v:
The Journal of the American Dental Association. 152:832-841.e4
Background In this study, the authors examine the cost-effectiveness of light-polymerized resin-based fluoride sealants on primary molars in high caries risk children younger than 6 years. Methods The authors examined the cost-effectiveness of pit-an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02d2351a5fe009d1f89f3400fe384251
https://doi.org/10.1016/j.adaj.2021.05.005
https://doi.org/10.1016/j.adaj.2021.05.005
Publikováno v:
Developmental Neuropsychology. 25:21-36
Children with closed head injury (CHI) perform poorly on complex tasks requiring working memory (WM). It is unclear to what extent WM itself is compromised, and whether WM varies with factors related to the CHI, such as injury severity, age at injury
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37d5181d6dc22c1e1780e5d9804536fd
https://doi.org/10.1207/s15326942dn2501&2_3
https://doi.org/10.1207/s15326942dn2501&2_3
Autor:
Rosemary Tannock, Jillian M. Couto, Barbara Anderson, Lissette Gomez, Tasha Cate-Carter, Tom Humphries, Karen Wigg, Jennifer Archibald, Elizabeth Kerr, Maureen W. Lovett, Cathy L. Barr
Publikováno v:
Journal of neurogenetics. 22(4)
A locus on chromosome 1p34-36 (DYX8) has been linked to developmental dyslexia or reading disabilities (RD) in three independent samples. In the current study, we investigated a candidate gene KIAA0319-Like (KIAA0319L) within DYX8, as it is homologou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f5c4842da825243d88bb38b537d58da
https://pubmed.ncbi.nlm.nih.gov/19085271
https://pubmed.ncbi.nlm.nih.gov/19085271
Autor:
Jennifer Archibald, Marcia A. Barnes, Lifang Zhang, Garland Roberson, Gerri Hanten, James Song, Maureen Dennis, Harvey S. Levin
Publikováno v:
Developmental neuropsychology. 25(1-2)
We studied the metacognitive functioning of children with severe and mild traumatic brain injury (TBI) and typically developing children. To test metacognition for memory, children were tested on a modified Judgment of Learning task. We found that ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4933f787b110eb78cd97033f758cc66d
https://pubmed.ncbi.nlm.nih.gov/14984330
https://pubmed.ncbi.nlm.nih.gov/14984330