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Duygu Onur Cura
Duygu Onur Cura
Denizli Devlet Hastanesi, Tıbbi Genetik
在 deu.edu.tr 的电子邮件经过验证
标题
引用次数
引用次数
年份
Genetik faktörlerin şiddet davranışı üzerine etkisi
DO Cura, T Çankaya
Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi 31 (2), 97-102, 2017
132017
Relationship between plasminogen activator inhibitor‐1 gene alterations and fibrosis in peritoneal dialysis patients
D Onur Cura, S Yildiz, E Ataman, S Ersan, M Tanrisev, A Ulgenalp, ...
Therapeutic Apheresis and Dialysis 25 (1), 97-102, 2021
12021
Chromosomal Evaluation Results for Transgender Individuals and Questioning the Necessity of Karyotyping
T Çankaya, D Onur Cura, H Özkalaycı, A Ulgenalp
Journal of Clinical Practice and Research 43 (2), 166, 2021
12021
Cinsiyet disforisinde genetik faktörlerin rolü
D Onur Cura, T Çankaya, A Ülgenalp
Hitit Medical Journal 2 (2), 49-55, 2020
1*2020
Unexpected Coexistence of a Derivative t (21; 21) and Complementary Mosaic r (21) in a Female with Multiple Miscarriages
D Onur Cura, E Bora, H Ozkalayci, O Kirbiyik, YB Kutbay, D Ercal, ...
Cytogenetic and Genome Research 158 (2), 83-87, 2019
12019
Broncholithiasis with recurrent lithoptysis: a case report
A Bircan, D Onur, A Yılmaz
Medical Principles and Practice 23 (1), 83-85, 2013
12013
How Much do we Know About the Findings of 22q11.2 Deletion Syndrome?: A Single-Centre Study with 11-Year Follow-Up
D Onur Cura, E Bora, O Giray Bozkaya, M Kir, D Ercal, T Cankaya
Journal of Basic and Clinical Health Sciences 4 (2), 114-117, 2020
2020
Comment on:“Gene–Diet Interactions in Type 2 Diabetes: The Chicken and Egg Debate”
D Onur Cura
International Journal of Molecular Sciences 20 (19), 4878, 2019
2019
Beslenme ve Genetik
D Onur Cura
Dahili Hastalarda Özel Beslenme ve Diyet Yönetimi, 57-73, 2019
2019
“Novel” Tiroid Stimüle Edici Hormon Reseptörü (TSHR) Mutasyonu Saptanan Konjenital Hipotiroidi Olgusu
D Onur Cura, A Ülgenalp
13. Uluslararası Katılımlı Ulusal Tıbbi Genetik Kongresi, 2019
2019
An Interesting Translocation Pattern With Phenotypically Normal Family A Daughter Inherited t(5,18) From The Mother With Two Independent Translocation t(1,2) t(5,18).
D Onur Cura, T Çankaya
13th Balkan Congress of Human Genetics, 2019
2019
Ağrı Genetiği
D Onur Cura
Orofasiyal, Baş ve Boyun Ağrılarına Multidisipliner Yaklaşım, 61-73, 2019
2019
Approach To A Case With 1p36 Deletion Via Molecular Genetic and Cytogenetics Methods
H Memiş, D Onur Cura, S Gürsoy, YB Kutbay, Ö Giray Bozkaya, ...
Erciyes Medical Journal 40 (2), 50, 2018
2018
A newborn with monosomy X in association with corpus callosum agenesis
DO Cura, B Iscan, S Gursoy, H Guleryuz, T Cankaya, T Ozturk, ...
Pediatrics & Neonatology 58 (5), 455-457, 2017
2017
Peritoneal Diyaliz Hastalarında PAi-1 Gen Değişimlerinin Fibrozisle Olan Ilişkisinin Araştırılması
DO Cura
PQDT-Global, 2017
2017
Three novel mutations of CHD7 gene in two turkish patients with charge syndrome; A double point mutation and an insertion
OG Bozkaya, E Ataman, C Randa, DO Cura, S Gürsoy, O Aksel, ...
Balkan Journal of Medical Genetics 18 (1), 65-70, 2015
2015
46,XX erkek sendromlu bir olgu
D Onur Cura, T Çankaya, Ö Öz, E Bora, A Ülgenalp, MD Erçal
Pediatri Uzmanlık Akademisi Dergisi 1 (4), 1-4, 2013
2013
The effect of genetics factors on agressive behavior
D Onur Cura, T Çankaya
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