| Genotype and phenotype evaluation of patients with primary ciliary dyskinesia: first results from Turkey N Emiralioğlu, EZ Taşkıran, C Koşukcu, E Bilgiç, P Atilla, B Kaya, ... Pediatric pulmonology 55 (2), 383-393, 2020 | 61 | 2020 |
| Etiology and outcome of hydrops fetalis: report of 62 cases S Takci, M Gharibzadeh, M Yurdakok, O Ozyuncu, A Korkmaz, Z Akcoren, ... Pediatrics & Neonatology 55 (2), 108-113, 2014 | 55 | 2014 |
| Does aeroallergen sensitivity and allergic rhinitis in children cause milder COVID-19 infection? E Vezir, M Hizal, BC Yayla, K Aykac, A Yilmaz, G Kaya, PD Oygar, ... Allergy and asthma proceedings 42 (6), 522, 2021 | 25 | 2021 |
| Diagnostic value of lung ultrasonography in children with COVID‐19 M Hizal, K Aykac, BCC Yayla, A Yilmaz, D Altun, HE Akkaya, GI Bayhan, ... Pediatric pulmonology 56 (5), 1018-1025, 2021 | 21 | 2021 |
| Developmental and behavioral problems in preschool-aged primary ciliary dyskinesia patients P Zengin Akkus, M Gharibzadeh Hizal, E Ilter Bahadur, EN Ozmert, ... European journal of pediatrics 178, 995-1003, 2019 | 15 | 2019 |
| Risk factors for recurrent pulmonary exacerbation in idiopathic pulmonary hemosiderosis M Hizal, S Eryilmaz Polat, T Ramasli Gursoy, B Ozsezen, ... Pediatric Pulmonology 56 (5), 1060-1068, 2021 | 11 | 2021 |
| Evaluation of pulmonary complications and affecting factors in children for repaired esophageal atresia and tracheoesophageal fistula GD Tuğcu, T Soyer, SE Polat, M Hizal, N Emiralioğlu, E Yalçın, D Doğru, ... Respiratory medicine 181, 106376, 2021 | 8 | 2021 |
| Nonmyeloablative hematopoietic stem cell transplantation in a patient with hereditary pulmonary alveolar proteinosis U Ozcelik, S Aytac, B Kuskonmaz, E Yalcin, D Dogru, V Okur, A Kara, ... Pediatric pulmonology 56 (2), 341-343, 2021 | 8 | 2021 |
| Respiratory viruses: What is their role in acute exacerbations in children with cystic fibrosis? M Hizal, E Yalcin, A Alp, M Ozden, J Karakaya, S Eryilmaz Polat, G Tugcu, ... Pediatric Pulmonology 55 (7), 1646-1652, 2020 | 8 | 2020 |
| Impact of mannose‐binding lectin 2 gene polymorphisms on disease severity in noncystic fibrosis bronchiectasis in children D Dogru, SE Polat, Ç Tan, İ Tezcan, SS Yalçın, E Utine, B Oğuz, İ Yaz, ... Pediatric Pulmonology 55 (5), 1190-1198, 2020 | 8 | 2020 |
| Levels of pro-and anti-inflammatory cytokines in cystic fibrosis patients with or without gingivitis O Duruel, E Berker, C Özşin-Özler, M Gharibzadeh-Hızal, Ö Gürpınar, ... Cytokine 127, 154987, 2020 | 8 | 2020 |
| Sleep disordered breathing in patients with Prader Willi syndrome: impact of underlying genetic mechanism B Ozsezen, N Emiralioglu, A Özön, O Akın, DA Tural, B Sunman, ... Respiratory medicine 187, 106567, 2021 | 6 | 2021 |
| Clinical features of pseudo-Bartter syndrome in cystic fibrosis M Hizal, K Ciki, S Esref, A Birbilen, G Tugcu, N Emiralioglu, E Yalcin, ... | 6 | 2017 |
| Obstructive sleep apnea in children with Down syndrome: is it possible to predict severe apnea? M Hizal, O Satırer, SE Polat, DA Tural, B Ozsezen, B Sunman, S Karahan, ... European Journal of Pediatrics, 1-9, 2022 | 5 | 2022 |
| The frequency and related factors of non‐tuberculosis mycobacteria infections among patients with cystic fibrosis D Ademhan Tural, N Emiralioglu, B Ozsezen, Z Saribas, N Ozcan, A Alp, ... Pediatrics International 63 (11), 1369-1375, 2021 | 5 | 2021 |
| Plasma ceramides and sphingomyelins of pediatric patients increase in primary ciliary dyskinesia but decrease in cystic fibrosis D Bal Topçu, G Tugcu, F Ozcan, M Aslan, A Yalcinkaya, SE Polat, M Hizal, ... Lipids 55 (3), 213-223, 2020 | 5 | 2020 |
| Geographical barriers to timely diagnosis of cystic fibrosis and anxiety level of parents during newborn screening in Turkey Y Gokdemir, TS Eyuboglu, N Emiralioglu, B Er, V Sen, S Pekcan, ... Pediatric Pulmonology 56 (10), 3223-3231, 2021 | 4 | 2021 |
| Differentially expressed genes associated with disease severity in siblings with cystic fibrosis İB Ekinci, M Hızal, N Emiralioğlu, U Özçelik, E Yalçın, D Doğru, N Kiper, ... Pediatric Pulmonology 56 (5), 910-920, 2021 | 4 | 2021 |
| Mutations of the CFTR gene and novel variants in Turkish patients with cystic fibrosis: 24-years experience D Dayangaç-Erden, M Atalay, N Emiralioğlu, M Hızal, S Polat, U Özçelik, ... Clinica Chimica Acta 510, 252-259, 2020 | 4 | 2020 |
| Two cases of Vici syndrome presenting with corpus callosum agenesis, albinism, and severe developmental delay M Hızal, B Yeke, Y Yıldız, A Öztürk, BB Gürbüz, T Coşkun The Turkish Journal of Pediatrics 62 (3), 474-478, 2020 | 4 | 2020 |
