Detalhe da pesquisa
1.
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.
Am J Hum Genet
; 104(4): 767-773, 2019 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30929741
2.
What we think about professional and unprofessional behaviors: differences between the perception of clinical faculty members and medical students.
BMC Med Educ
; 22(1): 866, 2022 Dec 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-36517813
3.
Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder.
Genet Med
; 23(7): 1246-1254, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33824500
4.
Pre-implantation genetic diagnosis in an Iranian family with a novel mutation in MUT gene.
BMC Med Genet
; 21(1): 22, 2020 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32013889
5.
Expanding the molecular and clinical phenotypes of FUT8-CDG.
J Inherit Metab Dis
; 43(4): 871-879, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32049367
6.
The protective effect of rifampicin on behavioral deficits, biochemical, and neuropathological changes in a cuprizone model of demyelination.
Cytokine
; 113: 417-426, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30539784
7.
2-(Bipiperidin-1-yl)-5-(nitroaryl)-1,3,4-thiadiazoles: Synthesis, evaluation of in vitro leishmanicidal activity, and mechanism of action.
Bioorg Med Chem
; 27(16): 3682-3691, 2019 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31300318
8.
A novel splice site mutation in WAS gene in patient with Wiskott-Aldrich syndrome and chronic colitis: a case report.
BMC Med Genet
; 19(1): 123, 2018 07 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-30029636
9.
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.
Am J Hum Genet
; 104(6): 1251, 2019 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31173719
10.
Infected Ruptured Pseudo-aneurysm in Descending Aorta; a Case Report.
Arch Acad Emerg Med
; 12(1): e23, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38572220
11.
The Efficacy of Long-Pulsed, 1064-nm Nd:YAG Laser Versus Aluminum Chloride 20% Solution in the Treatment of Axillary Hyperhidrosis.
J Lasers Med Sci
; 14: e71, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38318217
12.
WWFedCBMIR: World-Wide Federated Content-Based Medical Image Retrieval.
Bioengineering (Basel)
; 10(10)2023 Sep 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37892874
13.
Prenatal diagnosis of Sex determining region Y -box transcription factor 2 anophthalmia syndrome caused by germline mosaicism using next-generation sequencing: A case report.
Int J Reprod Biomed
; 21(8): 667-672, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37885978
14.
Deep Learning for Skin Melanocytic Tumors in Whole-Slide Images: A Systematic Review.
Cancers (Basel)
; 15(1)2022 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36612037
15.
Pre-Implantation Genetic Testing for Monogenic Disorders (PGT-M) in A Family with A Novel Mutation in DPAGT1 Gene.
Cell J
; 23(5): 593-597, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34837688
16.
Distribution of Class 1-3 Integrons in Carbapenem-Resistant Pseudomonas aeruginosa Isolated from Inpatients in Shiraz, South of Iran.
Ethiop J Health Sci
; 31(4): 719-724, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-34703170
17.
Identification of novel microsatellite markers flanking GJB2 gene in order to use in preimplantation genetic diagnosis of hearing loss: A comparison of whole-genome amplification and semi-nested PCR.
Eur J Med Genet
; 63(4): 103796, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31669356
18.
Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.
Front Genet
; 11: 585136, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33414805
19.
HIV-1 Tat protein attenuates the clinical course of experimental autoimmune encephalomyelitis (EAE).
Int Immunopharmacol
; 78: 105943, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31830622
20.
A comparative study on generating hydroxyl radicals by single and two-frequency ultrasound with gold nanoparticles and protoporphyrin IX.
Australas Phys Eng Sci Med
; 42(4): 1039-1047, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31617155