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2022 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus

Molecular Syndromology

Novel technique of cytolithotripsy for large bladder stones

6 6

2013 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

ASIAN JOURNAL OF ENDOSCOPIC SURGERY

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

0 0

2022 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

Functional & Integrative Genomics

Fluoroless ureteroscopy in whom and when

1 1

2015 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

UROLITHIASIS

The prevelance of human papillomavirus (HPV) genotypes detected by PCR in women with normal and abnormal cervico-vaginal cytology

0 0

2018 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

Ginekologia Polska

The Effect of Estrogen Usage on Eccentric Exercise Induced Damage in Rat Testes

0 0

2015 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

IRANIAN RED CRESCENT MEDICAL JOURNAL

The frequency of toll-like receptor 4 gene polymorphism in ankylosing spondylitis and its relationship between disease activity

0 0

2018 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

The European Research Journal

Pilates for Better Sex Changes in Sexual Functioning in Healthy Turkish Women After Pilates Exercise

13 13

2016 Özgün Makale SCI/SSCI/AHCI ESCI Scopus

JOURNAL OF SEX & MARITAL THERAPY

It Suddenly Occurred Extensive Subcutaneous Emphysema after Bipolar Transurethral Resection of Prostate

Aşırı aktif mesanede farmakoterapiye güncel bakış Current evaluation of pharmacotherapy for overactive bladder

Evaluation about complications of specialists in 2220 circumcision

The combination of furosemide and intravenoushydration does not affect the success of shock wavelithotripsy in renal stone treatment a prospectiverandomised single blinded trial

The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance

A Cause of Renal Dysfunction A Giant Bladder Stone

A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C&gt;T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels

Familial intragenic X-linked OPHN1 gene deletion in a newborn male infant with low birth weight and distinctive facial appearance that diagnosed by advanced microarray-CGH method

Copy number variations in patients with idiopathic recurrent pregnancy loss: an array- CGH approach

Brucellar epididymo orchitis A retrospective multicenter study of 28 cases and review of the literature

Are P-glycoprotein (ABCB1/MDR1) and endothelial nitric oxide synthase (eNOS) polymorphisms related to severity of the coronary artery disease?

PlasmaKinetic versus Cold Knife Internal Urethrotomy in Terms of Recurrence Rates A Prospective Randomized Study

A New Case of Rare Microdeletion 10q22.3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor Retardation