Detalhe da pesquisa
1.
Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome.
Am J Hum Genet
; 103(6): 968-975, 2018 12 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30414627
2.
Abuse-Deterrent Opioid Formulations and the Opioid Crisis: A Pharmacist's Perspective.
Ther Drug Monit
; 43(1): 35-41, 2021 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33278243
3.
The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis.
Genet Med
; 22(2): 389-397, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31388190
4.
Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis.
Genet Med
; 22(3): 669, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31844176
5.
CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum.
Genet Med
; 21(12): 2723-2733, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31239556
6.
Pregnancy and the Opioid Crisis: Heightened Effects of COVID-19.
J Addict Med
; 16(1): e2-e4, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34282083
7.
Brief intervention medication therapy management: Establishment of an opioid misuse intervention model delivered in a community pharmacy.
Am J Health Syst Pharm
; 78(4): 310-319, 2021 02 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33386733
8.
Addressing opioid use disorder among rural pregnant and postpartum women: a study protocol.
Addict Sci Clin Pract
; 15(1): 33, 2020 10 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-33129355
9.
Expanding the clinical and phenotypic heterogeneity associated with biallelic variants in ACO2.
Ann Clin Transl Neurol
; 7(6): 1013-1028, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32519519