Ahmet R. Ormeci
Istanbul, Turkey
Last Updated: 09/26/2026
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Found 13 publications
Is anterior segment OCT superior to slit-lamp biomicroscopic examination for Kayser Flesicher ring in Wilson's disease?
Journal: European review for medical and pharmacological sciences
Published: August 02, 2022
Amino acids and fatty acids in patients with beta thalassemia major.
Journal: Acta bio-medica : Atenei Parmensis
Published: April 16, 2018
Can Helicobacter pylori be eradicated with high-dose proton pump inhibitor in extensive metabolizers with the CYP2C19 genotypic polymorphism?
Journal: European review for medical and pharmacological sciences
Published: May 24, 2016
Effect of cytochrome P450 2C19 polymorphisms on the Helicobacter pylori eradication rate following two-week triple therapy with pantoprazole or rabeprazole.
Journal: European review for medical and pharmacological sciences
Published: March 25, 2016
VACTERL association with a rare vertebral anomaly (butterfly vertebra) in a case of monochorionic twin.
Journal: Genetic counseling (Geneva, Switzerland)
Published: July 26, 2014
A new case of holoprosencephaly-polydactyly syndrome with alobar holoprosencephaly, preaxial polydactyly and congenital glaucoma.
Journal: Genetic counseling (Geneva, Switzerland)
Published: May 03, 2014
Bamforth syndrome: is porencephaly a new finding?
Journal: Genetic counseling (Geneva, Switzerland)
Published: December 18, 2013
De novo terminal 4q deletion syndrome with new ocular findings in Turkish twins: case report.
Journal: Genetic counseling (Geneva, Switzerland)
Published: September 17, 2013
Seroepidemiology of pertussis in 10-15 years old healthy children in Isparta province, Turkey
Journal: Mikrobiyoloji bulteni
Published: August 27, 2013
Unilateral Renal Vein Thrombosis and Adrenal Hemorrhage in A Newborn with Homozygous Factor V Leiden and Heterozygous Of MTHFR-677T, MTHFR-1298C Gene Mutations.
Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
Published: July 08, 2013
A case of ring chromosome 13 with ambiguous genitalia and primary hypothyroidism.
Journal: Genetic counseling (Geneva, Switzerland)
Published: February 26, 2013
Last Updated: 09/26/2026