Detalhe da pesquisa
1.
A Systematic Review of Evidence-Based Treatments for Adolescent and Adult Sexual Assault Victims.
J Am Psychiatr Nurses Assoc
; 30(3): 480-502, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38148646
2.
Treatment Delays in Nonsyndromic Craniosynostosis: A 30-Year Retrospective Case-Control Analysis of the Impact of Socioeconomic and Family Status on Access to Care.
Ann Plast Surg
; 90(6S Suppl 5): S499-S508, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37399479
3.
Pediatric Orthognathic Surgery: A NSQIP-P Comparison of Peri-Operative Factors and Outcome Differences Between Cleft and Noncleft Patients.
Cleft Palate Craniofac J
; : 10556656221145079, 2022 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36542329
4.
New nurses apply only basic source evaluation criteria but realize their skills are lacking: More sophisticated approaches to teaching evaluation skills are required.
Health Info Libr J
; 39(2): 166-177, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-34424597
5.
Preclinical Development of EBI-005: An IL-1 Receptor-1 Inhibitor for the Topical Ocular Treatment of Ocular Surface Inflammatory Diseases.
Eye Contact Lens
; 44(3): 170-181, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28727604
6.
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus.
Am J Hum Genet
; 92(2): 210-20, 2013 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23332918
7.
The Gene Pool: The Ethics of Genetics in Primary Care.
Annu Rev Nurs Res
; 34: 119-54, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26673380
8.
Health literacy and obesity among native Hawaiian and Pacific Islanders in the United States.
Public Health Nurs
; 32(1): 15-23, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25273848
9.
Assessing genotype-phenotype correlation in Costello syndrome using a severity score.
Genet Med
; 15(7): 554-7, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23429430
10.
Cardiac anomalies in Axenfeld-Rieger syndrome due to a novel FOXC1 mutation.
Am J Med Genet A
; 161A(1): 114-9, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23239455
11.
Orthopedic manifestations and implications for individuals with Costello syndrome.
Am J Med Genet A
; 161A(8): 1940-9, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23813656
12.
The duplication 17p13.3 phenotype: analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes.
Am J Med Genet A
; 161A(8): 1833-52, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23813913
13.
Epidemiology and Etiology of Facial Injuries in Children.
Oral Maxillofac Surg Clin North Am
; 35(4): 515-519, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37302950
14.
Determining the affinities of high-affinity antibodies using KinExA and surface plasmon resonance.
MAbs
; 15(1): 2291209, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38088807
15.
Transmission of the rare HRAS mutation (c. 173C > T; p.T58I) further illustrates its attenuated phenotype.
Am J Med Genet A
; 158A(5): 1095-101, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22488832
16.
A novel HRAS substitution (c.266C>G; p.S89C) resulting in decreased downstream signaling suggests a new dimension of RAS pathway dysregulation in human development.
Am J Med Genet A
; 158A(9): 2106-18, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22821884
17.
Megalencephaly-capillary malformation (MCAP) and megalencephaly-polydactyly-polymicrogyria-hydrocephalus (MPPH) syndromes: two closely related disorders of brain overgrowth and abnormal brain and body morphogenesis.
Am J Med Genet A
; 158A(2): 269-91, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22228622
18.
Normative growth charts for individuals with Costello syndrome.
Am J Med Genet A
; 158A(11): 2692-9, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22887473
19.
Neurocognitive, adaptive, and behavioral functioning of individuals with Costello syndrome: a review.
Am J Med Genet C Semin Med Genet
; 157C(2): 115-22, 2011 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21495179
20.
Long-term survival in TARP syndrome and confirmation of RBM10 as the disease-causing gene.
Am J Med Genet A
; 155A(10): 2516-20, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21910224