Detalhe da pesquisa
1.
Depression in Patients with Peripheral Artery Disease: An Underdiagnosis with Increased Mortality.
Ann Vasc Surg
; 95: 80-86, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-36948397
2.
Simplified COI barcoding of blow, flesh, and scuttle flies encountered in medicolegal investigations.
Forensic Sci Med Pathol
; 2023 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37222900
3.
Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young.
Genome Res
; 26(9): 1170-7, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27435932
4.
Discovery of potent selective bioavailable phosphodiesterase 2 (PDE2) inhibitors active in an osteoarthritis pain model. Part II: optimization studies and demonstration of in vivo efficacy.
Bioorg Med Chem Lett
; 23(11): 3443-7, 2013 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23597790
5.
Discovery of potent, selective, bioavailable phosphodiesterase 2 (PDE2) inhibitors active in an osteoarthritis pain model, part I: transformation of selective pyrazolodiazepinone phosphodiesterase 4 (PDE4) inhibitors into selective PDE2 inhibitors.
Bioorg Med Chem Lett
; 23(11): 3438-42, 2013 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23582272
6.
The use of diary methods to evaluate daily experiences in first-episode psychosis.
Psychiatry Res
; 312: 114548, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35453098
7.
A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart.
Am J Hum Genet
; 83(2): 200-7, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18656178
8.
Vestibular dysfunction in DFNB1 deafness.
Am J Med Genet A
; 155A(5): 993-1000, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21465647
9.
Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment.
Am J Med Genet A
; 155A(6): 1298-313, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21538838
10.
Fitness among individuals with early childhood deafness: Studies in alumni families from Gallaudet University.
Ann Hum Genet
; 74(1): 27-33, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19930248
11.
Featured Counter-Trafficking Program: RELENTLESS.
Child Abuse Negl
; 100: 104140, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31445678
12.
Branchio-oto-renal syndrome (BOR): novel mutations in the EYA1 gene, and a review of the mutational genetics of BOR.
Hum Mutat
; 29(4): 537-44, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18220287
13.
Characteristics of obese children aged 1-4 years at a referral clinic.
J Natl Med Assoc
; 100(8): 884-91, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18717137
14.
Causes of fever in adults on the Thai-Myanmar border.
Am J Trop Med Hyg
; 74(1): 108-13, 2006 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16407353
15.
Effective teamwork and communication mitigate task saturation in simulated critical care air transport team missions.
Mil Med
; 179(8 Suppl): 19-23, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25102544
16.
Psychometric properties of a valuations scale for the Marijuana Effect Expectancies Questionnaire.
Addict Behav
; 38(3): 1629-34, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23254209
17.
Health of female sex workers and their children: a call for action.
Lancet Glob Health
; 4(7): e438-9, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27185469
18.
DNA testing of sexual assault evidence: the laboratory perspective.
J Forensic Nurs
; 7(3): 145-52, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21884402
19.
Compound heterozygosity for dominant and recessive GJB2 mutations: effect on phenotype and review of the literature.
Am J Med Genet A
; 143A(14): 1567-73, 2007 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17431919
20.
NSD1 analysis for Sotos syndrome: insights and perspectives from the clinical laboratory.
Genet Med
; 7(8): 524-33, 2005 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16247291