Yayınlar & Eserler

Yayın Ağı
SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

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) identifier identifier identifier

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 , sa.5, ss.608-617, 2024 (SCI-Expanded) identifier identifier

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) identifier identifier

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) identifier identifier

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 , 2023 (SSCI) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) identifier identifier identifier

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) Creative Commons License identifier identifier identifier identifier

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) Creative Commons License identifier identifier identifier

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) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier
Diğer Dergilerde Yayınlanan Makaleler

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) identifier

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) Creative Commons License identifier identifier

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) Sürdürülebilir Kalkınma identifier
Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

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

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

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

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
Metrikler

Yayın

18

Atıf (WoS)

7

H-İndeks (WoS)

1

Atıf (Scopus)

16

H-İndeks (Scopus)

2

Proje

1

Açık Erişim

4
BM Sürdürülebilir Kalkınma Amaçları