Detalhe da pesquisa
1.
Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic care.
Brain
; 145(3): 925-938, 2022 04 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35355055
2.
Discrimination and Adverse Perinatal Health Outcomes: A Latent Class Analysis.
Prev Chronic Dis
; 20: E96, 2023 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37917614
3.
Group vs traditional prenatal care for improving racial equity in preterm birth and low birthweight: the Centering and Racial Disparities randomized clinical trial study.
Am J Obstet Gynecol
; 227(6): 893.e1-893.e15, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36113576
4.
Membrane transporters in cell physiology, cancer metabolism and drug response.
Dis Model Mech
; 16(11)2023 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38037877
5.
Interdisciplinary views of fNIRS: Current advancements, equity challenges, and an agenda for future needs of a diverse fNIRS research community.
Front Integr Neurosci
; 17: 1059679, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36922983
6.
Palatal and oral manifestations of Muenke syndrome (FGFR3-related craniosynostosis).
J Craniofac Surg
; 23(3): 664-8, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22565872
7.
Using fNIRS to Identify Transparency- and Reliability-Sensitive Markers of Trust Across Multiple Timescales in Collaborative Human-Human-Agent Triads.
Front Neurogenom
; 3: 838625, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-38235468
8.
Advances in understanding illness anxiety.
Curr Psychiatry Rep
; 10(4): 311-7, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18627669
9.
Diffuse Gastric Ganglioneuromatosis: Novel Presentation of PTEN Hamartoma Syndrome-Case Report and Review of Gastric Ganglioneuromatous Proliferations and a Novel PTEN Gene Mutation.
Case Rep Med
; 2018: 4319818, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29770149
10.
Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature.
Am J Med Genet A
; 143A(24): 3204-15, 2007 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18000976
11.
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy.
Neurology
; 86(23): 2171-8, 2016 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27164704
12.
Novel mitochondrial DNA mutations associated with myopathy, cardiomyopathy, renal failure, and deafness.
Am J Med Genet A
; 140(20): 2216-22, 2006 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16955414