Yayınlar & Eserler

Yayın Ağı
Makaleler 8
Tümü (8)
SCI-E, SSCI, AHCI (8)
SCI-E, SSCI, AHCI, ESCI (8)
Scopus (8)
TRDizin (1)

1. Immunodeficiency-Associated Childhood Interstitial Lung Diseases: Data from the Türkiye chILD Registry

Kekeç H., ŞİŞMANLAR EYÜBOĞLU T., Tana Aslan A., MEDENİ V., ZİREK F., Tekin M., et al.
Balkan medical journal , cilt.43, sa.3, ss.125-135, 2026 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier

2. Variable Response to Elexacaftor/Tezacaftor/Ivacaftor in [L467F;F508del] Homozygous Patients: A Case Series

Akgül Erdal M., Yalçın E., Ceylan A. C., Dayangaç D., ERDEM ERALP E., EMİRALİOĞLU ORDUKAYA N., et al.
Pediatric Pulmonology , cilt.61, sa.2, 2026 (SCI-Expanded, Scopus) identifier identifier

3. Evaluation of postinfectious bronchiolitis obliterans patients in the Childhood Interstitial Lung Diseases Registry of Türkiye

KULA N., ASLAN A. T., ŞİŞMANLAR EYÜBOĞLU T., KEKEÇ H., Oksay S. C., Bilgin G., et al.
EUROPEAN RESPIRATORY JOURNAL , 2024 (SCI-Expanded, Scopus) identifier

4. Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study

Cavusoglu D., Ozturk G., TÜRKDOĞAN D., HIZ A. S., YİŞ U., Komur M., et al.
Cerebellum , 2024 (SCI-Expanded, Scopus) identifier identifier identifier

5. Sertoli-Leydig cell tumor, thyroid follicular carcinoma and rhabdomyosarcoma of the uterine cervix in a prepubertal girl with pathogenic germline variant in DICER1 gene

KARNAK İ., Ceylan A. C., HALİLOĞLU M., Ozon A., ORHAN D., Kutluk T.
TURKISH JOURNAL OF PEDIATRICS , cilt.63, sa.3, ss.500-505, 2021 (SCI-Expanded, Scopus) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

6. A special association between Charcot-Marie-Tooth type 1A disease and relapsing remitting multiple sclerosis

DOĞAN Y., GÜL Ş., Ceylan A. C., Kutsal Y. G.
MULTIPLE SCLEROSIS AND RELATED DISORDERS , cilt.35, ss.83-85, 2019 (SCI-Expanded, Scopus) identifier identifier identifier

7. Clinical heterogeneity associated with TUBB3 gene mutation in a Turkish family with congenital fibrosis of the extraocular muscles

CEYLAN A. C., Gursoy H., YILDIRIM N., BAŞMAK H., EROL N., ÇİLİNGİR O.
OPHTHALMIC GENETICS , cilt.38, sa.3, ss.288-290, 2017 (SCI-Expanded, Scopus) identifier identifier identifier

8. Two patients with microdeletion and microduplication involving 1q21.1

CEYLAN A. C., ÜTİNE G. E., ALİKAŞİFOĞLU M., BODUROĞLU O. K.
CHROMOSOME RESEARCH , cilt.23, 2015 (SCI-Expanded, Scopus) identifier
Metrikler

Yayın

8

Yayın (WoS)

8

Yayın (Scopus)

8

Atıf (WoS)

5

H-İndeks (WoS)

1

Atıf (Scopus)

1

H-İndeks (Scopus)

1

Açık Erişim

2
BM Sürdürülebilir Kalkınma Amaçları