Detalhe da pesquisa
1.
Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies.
Am J Hum Genet
; 110(11): 1919-1937, 2023 11 02.
Artigo
Inglês
| MEDLINE | ID: mdl-37827158
2.
Children's and adolescents' perspectives on living with advanced cancer: A meta-synthesis of qualitative research.
Qual Life Res
; 2024 May 25.
Artigo
Inglês
| MEDLINE | ID: mdl-38795197
3.
Use of Infrared Thermography in Medical Diagnosis, Screening, and Disease Monitoring: A Scoping Review.
Medicina (Kaunas)
; 59(12)2023 Dec 09.
Artigo
Inglês
| MEDLINE | ID: mdl-38138242
4.
De Novo Variants in MAPK8IP3 Cause Intellectual Disability with Variable Brain Anomalies.
Am J Hum Genet
; 104(2): 203-212, 2019 02 07.
Artigo
Inglês
| MEDLINE | ID: mdl-30612693
5.
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.
Am J Hum Genet
; 111(5): 996, 2024 May 02.
Artigo
Inglês
| MEDLINE | ID: mdl-38701747
6.
Seasonal changes in the abundance and activity of bacterial and fungal denitrifying communities associated with different compost amendments.
Can J Microbiol
; 68(2): 91-102, 2022 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-34762539
7.
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.
Am J Hum Genet
; 103(2): 221-231, 2018 08 02.
Artigo
Inglês
| MEDLINE | ID: mdl-30057030
8.
Minimal clinically important differences in the EORTC QLQ-C30 and brief pain inventory in patients undergoing re-irradiation for painful bone metastases.
Qual Life Res
; 27(4): 1089-1098, 2018 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-29188483
9.
Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.
Am J Hum Genet
; 103(3): 456, 2018 09 06.
Artigo
Inglês
| MEDLINE | ID: mdl-30193137
10.
Susceptibility of porcine endogenous retrovirus to anti-retroviral inhibitors.
Xenotransplantation
; 23(2): 151-8, 2016 03.
Artigo
Inglês
| MEDLINE | ID: mdl-27028725
11.
Classification of painful bone metastases as mild, moderate, or severe using both EORTC QLQ-C15-PAL and EORTC QLQ-BM22.
Support Care Cancer
; 24(12): 4871-4878, 2016 12.
Artigo
Inglês
| MEDLINE | ID: mdl-27465049
12.
Revisiting classification of pain from bone metastases as mild, moderate, or severe based on correlation with function and quality of life.
Support Care Cancer
; 24(4): 1617-23, 2016 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-26399406
13.
Minimal clinically important differences in the EORTC QLQ-BM22 and EORTC QLQ-C15-PAL modules in patients with bone metastases undergoing palliative radiotherapy.
Qual Life Res
; 25(10): 2535-2541, 2016 10.
Artigo
Inglês
| MEDLINE | ID: mdl-27138964
14.
Dexamethasone in the prophylaxis of radiation-induced pain flare after palliative radiotherapy for bone metastases: a double-blind, randomised placebo-controlled, phase 3 trial.
Lancet Oncol
; 16(15): 1463-1472, 2015 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-26489389
15.
Single versus multiple fractions of repeat radiation for painful bone metastases: a randomised, controlled, non-inferiority trial.
Lancet Oncol
; 15(2): 164-71, 2014 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-24369114
16.
Dacomitinib compared with placebo in pretreated patients with advanced or metastatic non-small-cell lung cancer (NCIC CTG BR.26): a double-blind, randomised, phase 3 trial.
Lancet Oncol
; 15(12): 1379-88, 2014 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-25439692
17.
Assessment of osteopontin in early breast cancer: correlative study in a randomised clinical trial.
Breast Cancer Res
; 16(1): R8, 2014 Jan 22.
Artigo
Inglês
| MEDLINE | ID: mdl-24451146
18.
Patient Factors Associated with Missed Otolaryngology Appointments at an Urban Safety-Net Hospital.
Laryngoscope
; 2024 Apr 11.
Artigo
Inglês
| MEDLINE | ID: mdl-38602281
19.
Detailed mapping of determinants within the porcine endogenous retrovirus envelope surface unit identifies critical residues for human cell infection within the proline-rich region.
J Virol
; 86(17): 9096-104, 2012 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-22696659
20.
American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing.
Genet Med
; 15(2): 150-2, 2013 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-23328890