Kismet Çıkı (Kısmet Çıkı)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 8

Top Topics

End Stage Renal Disease

Polycyclic Aromatic Hydrocarbons

Hypertrophic Cardiomyopathy

Top Venues

Journal of pediatric endocrinology & metabolism : JPEM

Metabolic brain disease

Balkan medical journal

Klinische Padiatrie

This page only lists publications with an associated author ORCID identifier.

Publications

Ceren Alavanda, Emine İpek Ceylan, Sebile Kılavuz, Kismet Çıkı
Comprehensive analyses of phenylalanine hydroxylase variants and phenotypic characteristics of patients in the eastern region of Türkiye. Journal of pediatric endocrinology & metabolism : JPEM 37 (6) (2024)
Ceren Alavanda, Emine İpek Ceylan, Sebile Kılavuz, Kismet Çıkı
Comprehensive analyses of phenylalanine hydroxylase variants and phenotypic characteristics of patients in the eastern region of Türkiye. Journal of pediatric endocrinology & metabolism : JPEM (2024)
Ceren Alavanda, Emine İpek Ceylan, Sebile Kılavuz, Kismet Çıkı
Comprehensive analyses of phenylalanine hydroxylase variants and phenotypic characteristics of patients in the eastern region of Türkiye. Journal of pediatric endocrinology & metabolism : JPEM 37 (6) (2024)
Kismet Çıkı, Rıza Köksal Özgül, Yılmaz Yildiz
Genetic Counseling for Phenylketonuria Complicated by Undiagnosed Parental Hyperphenylalaninemia in a Single Family. Klinische Padiatrie (2022)
Kismet Çıkı, H Tuna Akar, R Köksal Özgül, Basri Gülbakan, Yilmaz Yildiz
Perplexing Etiology of Hyperphenylalaninemia in an Infant Referred via Newborn Screening. Clinical chemistry 67 (10) (2022)
Özge Yanık, Kismet Çıkı, Emin Ozmert, Hatice Serap Sivri
Vascular and structural analyses of retinal and choroidal alterations in Fabry disease: the effect of hyperreflective foci and retinal vascular tortuosity. Ophthalmic genetics 43 (3) (2022)
Halil Tuna Akar, Yilmaz Yildiz, Gökhan Güvenkaya, Kismet Çıkı, Ayça Burcu Kahraman, Izzet Erdal, Turgay Coşkun, Hatice Serap Sivri, Ayşegül Tokatlı
Single Institutional Experience with GM1 Gangliosidosis: Clinical and Laboratory Results of 14 Patients Balkan medical journal 39 (5) (2022)
Kismet Çıkı, Yilmaz Yildiz, Didem Yücel Yılmaz, Emine Pektaş, Ayşegül Tokatlı, Rıza Köksal Özgül, Hatice Serap Sivri, Ali Dursun
DNACJ12 deficiency in patients with unexplained hyperphenylalaninemia: two new patients and a novel variant. Metabolic brain disease 36 (6) (2021)