Metrikler
Yayın
23
Açık Erişim
4
BM Sürdürülebilir Kalkınma Amaçları
Araştırma Alanları
Tıp
Akademik Faaliyetlere Dayalı Araştırma Alanları
Avesis Araştırma Alanları
WoS Araştırma Alanları
Scopus Araştırma Alanları
Makaleler
Tümü (19)
SCI-E, SSCI, AHCI (15)
SCI-E, SSCI, AHCI, ESCI (17)
ESCI (2)
Scopus (16)
TRDizin (6)
2025
20251. Glutathione synthetase deficiency: severe hemolysis and metabolic acidosis with symptoms in the intrauterine period
Demirsu A., Aliyev F., Yucel E., ÇIKI K., YILDIZ Y., Urel-Demir G., et al.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
, 2025 (SCI-Expanded, Scopus)
2025
20252. A comprehensive integrated disease management program for phenylketonuria (IDMP-PKU) from Türkiye: rationale, design and patient characteristics
BALCI M. C., KOR D., YILDIZ Y., KARACA M., BULUT F. D., Kahraman A. B., et al.
ORPHANET JOURNAL OF RARE DISEASES
, cilt.20, sa.1, 2025 (SCI-Expanded, Scopus)
2025
20253. Comprehensive analysis of 1103 infants referred to a single center due to positive newborn screening test for phenylketonuria
KAHRAMAN A. B., ÇIKI K., POŞUL B., Guvercin M., YILDIZ Y., DURSUN A., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.67, sa.2, ss.175-185, 2025 (SCI-Expanded, Scopus, TRDizin)
2025
20254. Clinical and laboratory characteristics of propionic acidemia in a Turkish cohort
AKAR H. T., KAHRAMAN A. B., YILDIZ Y., Baran B., ÇIKI K., COŞKUN T., et al.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
, sa.4, ss.399-405, 2025 (SCI-Expanded, Scopus)
2025
20255. Impact of the COVID-19 Era on Phenylalanine Levels and Classical Phenylketonuria Patients Follow-Up: A Retrospective Analysis
KAHRAMAN A. B., YILDIZ Y., GEÇİCİ N. N., ÇIKI K., ERDAL İ., AKAR H. T., et al.
Türkiye Çocuk Hastalıkları Dergisi
, cilt.19, sa.2, ss.59-63, 2025 (TRDizin)
2025
20256. High prevalence of low bone mineral density in young adults with phenylketonuria
ÇIKI K., KAHRAMAN A. B., AKAR H. T., YILDIZ Y., DURSUN A., Tokatli A., et al.
POSTGRADUATE MEDICINE
, sa.1, ss.86-92, 2025 (SCI-Expanded, Scopus)
2024
20247. Comprehensive analysis of genotypic and phenotypic characteristics of biotinidase deficiency patients in the eastern region of Türkiye
Ciki K., Alavanda C., Ceylan E. I., Tanyalcin T., Kilavuz S.
TURKISH JOURNAL OF PEDIATRICS
, cilt.66, sa.5, ss.608-617, 2024 (SCI-Expanded, Scopus, TRDizin)
2023
20238. Predictors of eventual requirement of phenylalanine-restricted diet in young infants with phenylalanine hydroxylase deficiency initially managed with sapropterin monotherapy
ÇIKI K., YILDIZ Y., KAHRAMAN A. B., ÖZGÜL R. K., COŞKUN T., DURSUN A., et al.
Molecular Genetics and Metabolism
, cilt.140, sa.3, 2023 (SCI-Expanded, Scopus)
2023
20239. Efficacy of Tele-CO-OP in Children With Organic Acidemia: A Pilot Randomized Controlled Trial
Dursun E. L., BUMİN G., ÇIKI K., SİVRİ S.
OTJR Occupation, Participation and Health
, sa.3, ss.417-425, 2023 (SSCI, Scopus)
2023
202310. COVID-19 in inherited metabolic disorders: Clinical features and risk factors for disease severity
KAHRAMAN A. B., YILDIZ Y., ÇIKI K., Erdal I., AKAR H. T., DURSUN A., et al.
Molecular Genetics and Metabolism
, cilt.139, sa.2, 2023 (SCI-Expanded, Scopus)
2022
202211. Vascular and structural analyses of retinal and choroidal alterations in Fabry disease: the effect of hyperreflective foci and retinal vascular tortuosity
YANIK ODABAŞ Ö., ÇIKI K., ÖZMERT E., Sivri S.
OPHTHALMIC GENETICS
, cilt.43, sa.3, ss.344-353, 2022 (SCI-Expanded, Scopus)
2021
202112. Evaluation of sleep-disordered breathing and its relationship with respiratory parameters in children with mucopolysaccharidosis Type IVA and VI
Ademhan Tural D., EMİRALİOĞLU N., DOĞRU ERSÖZ D., Ozsezen B., Ipek O. F., SUNMAN B., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
, cilt.185, sa.8, ss.2306-2314, 2021 (SCI-Expanded, Scopus)
2021
202113. The Complication of Endotracheal Intubation in a Patient with Mucopolysaccharidosis Type IIIA
Tural D. A., EMİRALİOĞLU N., Ozsezen B., ÇIKI K., Ozcan N., ARDIÇLI B., et al.
INTERNATIONAL JOURNAL OF PEDIATRICS-MASHHAD
, cilt.9, sa.2, ss.12909-12913, 2021 (ESCI)
2021
202114. Cardiomyopathy in patients with type 1 tyrosinemia, and the effect of nitisinone treatment on cardiomyopathy
BİLGİNER GÜRBÜZ B., AYKAN H. H., ÇIKI K., KARAGÖZ T., Sivri S., DURSUN A., et al.
CUKUROVA MEDICAL JOURNAL
, cilt.46, sa.4, ss.1419-1425, 2021 (ESCI, TRDizin)
2020
202015. Caring for a Child with Phenylketonuria: Parental Experiences from a Eurasian Country
ZENGİN AKKUŞ P., BİLGİNER GÜRBÜZ B., ÇIKI K., İLTER BAHADUR E., KARAHAN S., ÖZMERT E. N., et al.
JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS
, cilt.41, sa.3, ss.195-202, 2020 (SCI-Expanded, SSCI, Scopus)
2020
202016. A rare cause of acute abdominal pain in a patient with Primary ciliary dyskinesia with situs inversus totalis
Ciki K., Turer Ö., Hizal M., Tugcu G. D., EMİRALİOĞLU N., Yalcin E., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.62, sa.1, ss.156-159, 2020 (SCI-Expanded, Scopus, TRDizin)
2019
201917. Pulmonary complications following hematopoietic stem cell transplantation in children
ÇIKI K., DOĞRU ERSÖZ D., Kuskonmaz B. B., EMİRALİOĞLU N., Yalcin E., Ozcelik U., et al.
TURKISH JOURNAL OF PEDIATRICS
, cilt.61, sa.1, ss.59-70, 2019 (SCI-Expanded, Scopus, TRDizin)
2017
201718. A fatal Clostridium perfringens infection with hemolysis after chemotherapy in an adolescent
Kukul M. G., Ciki K., Karadag-Oncel E., CENGİZ A. B., Kuskonmaz B. B., Tavil B., et al.
ARCHIVOS ARGENTINOS DE PEDIATRIA
, cilt.115, sa.2, 2017 (SCI-Expanded, Scopus)
2017
201719. Clinical evaulation of patients with congenital lung malformations Konjenital akciger malformasyonu olan hastalarin klinik degerlendirmesi
EMİRALİOĞLU N., Çiki K., Tugcu G. D., Yalçin E., Ersöz D., Kiper N., et al.
Cocuk Sagligi ve Hastaliklari Dergisi
, cilt.60, sa.1, ss.1-6, 2017 (Scopus)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
2019
20191. Listening Parents Caring A Child With Phenylketonuria
ZENGİN AKKUŞ P., BİLGİNER GÜRBÜZ B., ÇIKI K., İLTER BAHADUR E., KARAHAN S., ÖZMERT E. N., et al.
3rd International Developmental Pediatrics Association Congress, 9 - 12 Aralık 2019, (Özet Bildiri)
2019
20192. Fenilketonüri ile Yaşamak: Anne Ve Babaların Penceresinden
ZENGİN AKKUŞ P., BİLGİNER GÜRBÜZ B., ÇIKI K., İLTER BAHADUR E., KARAHAN S., ÖZMERT E. N., et al.
63. Türkiye Milli Pediatri Kongresi, Türkiye, 30 Ekim - 03 Kasım 2019, (Özet Bildiri)
2019
20193. Hyperphenylalaninemia due to novel JCDNA12 mutation
SİVRİ H. S., ÇIKI K., YÜCEL YILMAZ D., GÜRSES CİLA H. E., ÖZGÜL R. K., TOKATLI A., et al.
SSIEM 2019: Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Rotterdam, Hollanda, 3 - 06 Eylül 2019, cilt.42, ss.324, (Özet Bildiri)
2017
20174. Antibiotic resistance of Haemophilus influenzae in primary Ciliary Dyskinesia patients
ÇIKI K., SANCAK B., DEMİRCİ S., EMİRALİOĞLU N., TUĞCU G. D., EŞREF S., et al.
2nd BEAT-PCD Conference and 3rd PCD training School, Valencia, İspanya, 18 - 21 Nisan 2017, (Özet Bildiri)