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European Journal of Medical Genetics|April 3, 2020
A homozygote frameshift mutation in OCLN gene result in Pseudo-TORCH syndrome type I: A case report extending the phenotype with central diabetes insipidus and renal dysfunctionFaruk Ekinci, Riza Dincer Yildizdas, Ozden Ozgur Horoz, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|February 12, 2013
Pollen aero allergens and the climate in Mediterranean region and allergen sensitivity in allergic rhinoconjunctivitis and allergic asthma patientsArzu Didem Yalcin, Saime Basaran, Atil Bisgin, et al.
Human Gene Therapy|April 16, 2021
Current Update on Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Development with a Special Emphasis on Gene Therapy Viral Vector Design and Construction for VaccinationAtil Bisgin, Ahter D Sanlioglu, Yunus Emre Eksi, et al.
JPMA. the Journal of the Pakistan Medical Association|April 5, 2021
The cumulative effects of MEFV gene polymorphisms and mutations in patients with inflammatory bowel diseasesMehmet Agin, Atil Bisgin, Mustafa Yilmaz, et al.
European Journal of Medical Genetics|September 19, 2017
A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitisRabia Miray Kisla Ekinci, Sibel Balci, Atil Bisgin, et al.
Rheumatology International|March 7, 2020
Altered expression of apoptosis-related, circulating cell-free miRNAs in children with familial Mediterranean fever: a cross-sectional studyEmin Murat Karpuzoglu, Rabia Miray Kisla Ekinci, Sibel Balci, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|October 3, 2013
Increased serum S-TRAIL level in newly diagnosed stage-IV lung adenocarcinoma but not squamous cell carcinoma is correlated with age and smokingAysegul Kargi, Atil Bisgin, Arzu Didem Yalcin, et al.
CEN Case Reports|May 7, 2020
Recurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency?Rabia Miray Kisla Ekinci, İbrahim Altun, Atil Bisgin, et al.
Annals of Indian Academy of Neurology|February 24, 2021
Different Clinical Manifestations of Three Prime Repair Exonuclease 1 Mutation: A Case SeriesFaruk Incecik, Sibel Balci, Rabia Miray Kisla Ekinci, et al.
Scottish Medical Journal|March 14, 2019
Hyperimmunoglobulinemia D syndrome with recurrent perianal abscess successfully treated with canakinumabRabia Miray Kisla Ekinci, Sibel Balcı, Atil Bisgin, et al.
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