Detalhe da pesquisa
1.
Neuromuscular disease genetics in under-represented populations: increasing data diversity.
Brain
; 146(12): 5098-5109, 2023 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37516995
2.
Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency.
Eur J Pediatr
; 183(3): 1341-1351, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38141137
3.
Impact of Inflammation-Related Genes on COVID-19: Prospective Study at Turkish Cohort.
Tohoku J Exp Med
; 261(3): 179-185, 2023 Nov 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37635061
4.
Clinical and Demographic Characteristics of Cutaneous Mastocytosis in Childhood: Single-center Experience.
J Pediatr Hematol Oncol
; 44(1): e227-e232, 2022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34001789
5.
Contribution of Inherited Variants to Hereditary Cancer Syndrome Predisposition.
Tohoku J Exp Med
; 258(4): 319-325, 2022 11 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36288950
6.
The effectiveness of anti-interleukin-1 therapy on subclinical inflammation parameters during the attack-free period in familial Mediterranean fever patients: A case-control study.
Turk J Med Sci
; 52(2): 522-523, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36161616
7.
The effectiveness of anti-interleukin-1 therapy on subclinical inflammation parameters during the attack-free period in familial Mediterranean fever patients: A case-control study.
Turk J Med Sci
; 52(2): 494-504, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-38812979
8.
Phenotype 2 familial mediterranean fever: evaluation of 22 case series and review of the literature on phenotype 2 FMF.
Ren Fail
; 35(2): 226-30, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23228227
9.
Relationship between asthma and IL-17 gene polymorphism in a Turkish population.
Ir J Med Sci
; 192(1): 269-275, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-35325374
10.
High diagnostic yield with algorithmic molecular approach on hereditary neuropathies.
Rev Assoc Med Bras (1992)
; 69(2): 233-239, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36790232
11.
Determination of homeodomain interacting protein kinase 2 polymorphisms rs2058265, rs6464214, and rs7456421 in patients with kidney stone.
Cir Cir
; 91(4): 474-478, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37677956
12.
Low plasma vitamin D levels in patients with familial Mediterranean fever.
Rheumatol Int
; 32(12): 3845-9, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22193220
13.
Concomitance of Gitelman syndrome and familial Mediterranean fever: a rare case presentation.
Ren Fail
; 34(10): 1333-4, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23009175
14.
Are angiotensin converting enzyme (ACE1/ACE2) gene variants associated with the clinical severity of COVID-19 pneumonia? A single-center cohort study.
Anatol J Cardiol
; 26(2): 133-140, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35190362
15.
Emphasis of FAS/FASL gene polymorphism in patients with non-muscle invasive bladder cancer.
Ir J Med Sci
; 187(4): 1115-1119, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-29453645
16.
The increased expression of Piezo1 and Piezo2 ion channels in human and mouse bladder carcinoma.
Adv Clin Exp Med
; 27(8): 1025-1031, 2018 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-30010255
17.
High diagnostic yield with algorithmic molecular approach on hereditary neuropathies
Rev. Assoc. Med. Bras. (1992, Impr.)
; 69(2): 233-239, Feb. 2023. tab
Artigo
em Inglês
|
LILACS-Express
| ID: biblio-1422632
18.
Clinical characteristics and HLA alleles of a family with simultaneously occurring alopecia areata.
Cutis
; 97(6): E30-6, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27416096
19.
Potential role of melastatin-related transient receptor potential cation channel subfamily M gene expression in the pathogenesis of urinary bladder cancer.
Oncol Lett
; 12(6): 5235-5239, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28101241
20.
Focal epithelial hyperplasia associated with human papillomavirus 13 and common human leukocyte antigen alleles in a Turkish family.
Int J Dermatol
; 54(2): 174-8, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24738569