Detalhe da pesquisa
1.
Emergence of acute promyelocytic leukemia in a patient with granulomatosis with polyangiitis during treatment with cyclophosphamide: a rare case report.
Reumatismo
; 75(4)2023 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38115775
2.
Enhancing the Vortex Whistle for Measures of Respiratory Capacity Via Computational Fluid Dynamics and Computational Aero-Acoustic Analysis.
J Biomech Eng
; 144(11)2022 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35579176
3.
Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse.
PLoS Genet
; 14(3): e1007297, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29590114
4.
Persistent confirmed low-grade dysplasia in Barrett's esophagus is a risk factor for progression to high-grade dysplasia and adenocarcinoma in a US Veterans cohort.
Dis Esophagus
; 33(2)2020 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31274147
5.
Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss.
Hum Mutat
; 40(1): 53-72, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30303587
6.
Human neonatal stem cell-derived skin substitute improves healing of severe burn wounds in a rat model.
Cell Biol Int
; 43(2): 147-157, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30443955
7.
Inframe deletion of human ESPN is associated with deafness, vestibulopathy and vision impairment.
J Med Genet
; 55(7): 479-488, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29572253
8.
A biomarker panel predicts progression of Barrett's esophagus to esophageal adenocarcinoma.
Dis Esophagus
; 32(1)2019 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30496496
9.
Dysplasia severity is associated with poor quality of life in patients with Barrett's esophagus referred for endoscopic eradication therapy.
Dis Esophagus
; 32(1)2019 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30169612
10.
Spectral/Cepstral Analyses of Phonation in Parkinson's Disease before and after Voice Treatment: A Preliminary Study.
Folia Phoniatr Logop
; 71(5-6): 275-285, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31117110
11.
Impact of smoking, alcohol consumption, and NSAID use on risk for and phenotypes of eosinophilic esophagitis.
Dis Esophagus
; 31(1): 1-7, 2018 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29025076
12.
Natural history of eosinophilic esophagitis: a systematic review of epidemiology and disease course.
Dis Esophagus
; 31(8)2018 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29617744
13.
Validation of a biomarker panel in Barrett's esophagus to predict progression to esophageal adenocarcinoma.
Dis Esophagus
; 31(11)2018 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29635420
14.
Association of sporadic and familial Barrett's esophagus with breast cancer.
Dis Esophagus
; 31(4)2018 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29528378
15.
Whole-Exome Sequencing Identifies Novel Variants that Co-segregates with Autosomal Recessive Retinal Degeneration in a Pakistani Pedigree.
Adv Exp Med Biol
; 1074: 219-228, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29721947
16.
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome.
PLoS Genet
; 11(3): e1005097, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25807530
17.
Transplantation of stromal-derived factor 1α and basic fibroblast growth factor primed insulin-producing cells reverses hyperglycaemia in diabetic rats.
Growth Factors
; 35(2-3): 88-99, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28835141
18.
Serum from CCl4-induced acute rat injury model induces differentiation of ADSCs towards hepatic cells and reduces liver fibrosis.
Growth Factors
; 35(4-5): 144-160, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29110545
19.
Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86.
Am J Hum Genet
; 94(1): 144-52, 2014 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-24387994
20.
The role of Heller myotomy and POEM for nonachalasia motility disorders.
Dis Esophagus
; 30(4): 1-5, 2017 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28375487