Sema Kalkan Uçar (Sema Kalkan Ucar, Sema Kalkan Ucar, Sema K Uçar)

Publication Activity (10 Years)

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

Top Topics

Duchenne Muscular Dystrophy

Psychometric Properties

End Stage Renal Disease

Top Venues

Journal of pediatric endocrinology & metabolism : JPEM

Archivos argentinos de pediatria

Journal of inherited metabolic disease

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

Publications

Ilayda Korkmaz, Sema Kalkan Uçar, Hüseyin Onay, Eser Yıldırım Sözmen, Mahmut Çoker, Melis Palamar
Ocular Manifestations of Fabry Disease: Report from a Tertiary Eye Care Center in Türkiye. Turkish journal of ophthalmology 54 (3) (2024)
Sema Kalkan Uçar, Yasemin Atik Altınok, Yelda Mansuroglu, Ebru Canda, Havva Yazıcı, Merve Yoldas Çelik, Fehime Erdem, Ayşe Yüksel Yanbolu, Zülal Ülger, Mahmut Coker
Long-term personalized high-protein, high-fat diet in pediatric patients with glycogen storage disease type IIIa: Evaluation of myopathy, metabolic control, physical activity, growth, and dietary compliance. Journal of inherited metabolic disease (2024)
Merve Yoldas Çelik, Havva Yazıcı, Fehime Erdem, Ayse Yuksel Yanbolu, Ayca Aykut, Asude Durmaz, Selcan Zeybek, Ebru Canda, Sema Kalkan Uçar, Mahmut Coker
Unique clinical presentations and follow-up outcomes from experience with congenital disorders of glycosylation: PMM2-PGM1-DPAGT1-MPI-POMT2-B3GALNT2-DPM1-SRD5A3-CDG. Journal of pediatric endocrinology & metabolism : JPEM (2023)
Havva Yazıcı, Gunes Ak, Merve Yoldas Çelik, Fehime Erdem, Ayse Yuksel Yanbolu, Esra Er, Ayse Ergul Bozaci, Merve Saka Güvenç, Ayça Aykut, Asude Alpman Durmaz, Ebru Canda, Sema Kalkan Uçar, Mahmut Coker
Experience with carnitine palmitoyltransferase II deficiency: diagnostic challenges in the myopathic form. Journal of pediatric endocrinology & metabolism : JPEM (2023)
Havva Yazıcı, Ebru Canda, Sema Kalkan Uçar, Mahmut Coker
Severe perinatal hypophosphatasia case with a novel mutation. Archivos argentinos de pediatria 120 (1) (2022)
Murat Ç Karataş, Havva Yazıcı, Ayse Ergul Bozaci, Ebru Canda, Reşit Ertürk Levent, Sema Kalkan Uçar, Mahmut Coker
Rare coexistence of Tay-Sachs disease, coarctation of the aorta and grade V vesicoureteral reflux. Archivos argentinos de pediatria 120 (1) (2022)
Sema Kalkan Uçar, Havva Yazıcı, Ebru Canda, Esra Er, Fatma Derya Bulut, Cenk Eraslan, Hüseyin Onay, Bridget Elizabeth Bax, Mahmut Çoker
Clinical spectrum of early onset "Mediterranean" (homozygous p.P131L mutation) mitochondrial neurogastrointestinal encephalomyopathy. JIMD reports 63 (5) (2022)
Ayse Ergul Bozaci, Havva Yazıcı, Ebru Canda, Sema Kalkan Uçar, Merve Saka Guvenc, Afig Berdeli, Sara Habif, Mahmut Coker
Long-term follow-up of alkaptonuria patients: single center experience. Journal of pediatric endocrinology & metabolism : JPEM 35 (7) (2022)
Havva Yazici, Ebru Canda, Yasemin Atik Altınok, Sema Kalkan Uçar, Mahmut Coker
Two siblings with galactose mutarotase deficiency: Clinical differences. JIMD reports 63 (1) (2021)
Ayse Ergul Bozaci, Esra Er, Havva Yazici, Ebru Canda, Sema Kalkan Uçar, Merve Güvenc Saka, Cenk Eraslan, Hüseyin Onay, Sara Habif, Beat Thöny, Mahmut Coker
Tetrahydrobiopterin deficiencies: Lesson from clinical experience. JIMD reports 59 (1) (2021)