Detalhe da pesquisa
1.
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Funct Integr Genomics
; 22(3): 291-315, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35098403
2.
The effect of neoadjuvant chemotherapy on tumor-infiltrating lymphocytes in patients with breast cancer.
Future Oncol
; 18(29): 3289-3298, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-36017739
3.
Unusual Chromosomal Rearrangement Resulted in Interstitial Monosomy 9p: Case Report.
Cytogenet Genome Res
; 148(1): 19-24, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27166162
4.
AUTS2 Syndrome in a 68-year-old female: Natural history and further delineation of the phenotype.
Am J Med Genet A
; 170(12): 3231-3236, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27531620
5.
Clinical and inflammation marker features of cancer patients with COVID-19: data of Istanbul, Turkey multicenter cancer patients (2020-2022).
Curr Med Res Opin
; 39(7): 987-996, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37300513
6.
MCM-2 Levels as a Potential Biomarker for Predicting High-Risk Breast Cancer Patients According to TAILORx Classification.
Breast Cancer (Dove Med Press)
; 15: 659-669, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37674872
7.
Survival results according to Oncotype Dx recurrence score in patients with hormone receptor positive HER-2 negative early-stage breast cancer: first multicenter Oncotype Dx recurrence score survival data of Turkey.
Front Oncol
; 13: 1151733, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37448522
8.
Evaluation of Anti-Mullerian Hormone Levels, Antral Follicle Counts, and Mean Ovarian Volumes in Chemotherapy-Induced Amenorrhea among Breast Cancer Patients: A Prospective Clinical Study.
Curr Oncol
; 30(10): 9217-9229, 2023 10 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37887566
9.
Hypomyelinating spastic dyskinesia and ichthyosis caused by a homozygous splice site mutation leading to exon skipping in ELOVL1.
Brain Dev
; 44(6): 391-400, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35379526
10.
Importance of multigene panel test in patients with consanguineous marriage and family history of breast cancer.
Oncol Lett
; 23(4): 118, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-35261632
11.
Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia.
J Pediatr Endocrinol Metab
; 34(9): 1201-1205, 2021 Sep 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34142517
12.
The miRNA content of circulating exosomes in DLBCL patients and in vitro influence of DLBCL-derived exosomes on miRNA expression of healthy B-cells from peripheral blood.
Cancer Biomark
; 32(4): 519-529, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34275894
13.
Prevalence and clinical/molecular characteristics of PTEN mutations in Turkish children with autism spectrum disorders and macrocephaly.
Mol Genet Genomic Med
; 9(8): e1739, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34268892
14.
Prenatal diagnsis of intracardiac hamartoma and Turner syndrome.
Fetal Pediatr Pathol
; 29(5): 330-7, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20704479
15.
Prenatal diagnosis of VACTERL syndrome and partial caudal regression syndrome: a previously unreported association.
J Clin Ultrasound
; 37(8): 464-6, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19536863
16.
First Observation of Hemoglobin Jabalpur [Beta 3 (NA3) Leu>Pro] in the Turkish Population.
Turk J Haematol
; 31(3): 319-20, 2014 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25330532
17.
DNA fragmentation index and human papilloma virus in males with previous assisted reproductive technology failures.
Turk J Urol
; 45(1): 12-16, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29975635
18.
First Observation of Hb South Florida [beta 1(NA1) Val>Met] in Turkey.
Turk J Haematol
; 30(2): 223-4, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24385794
19.
Clonal evolution of monosomy 7 in acquired severe aplastic anemia: Two cases treated with allogeneic hematopoietic stem cell transplantation.
Turk J Haematol
; 25(2): 94-7, 2008 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27264447
20.
A Large PROP1 Gene Deletion in a Turkish Pedigree.
Case Rep Endocrinol
; 2018: 2403430, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30112224