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Hasan Önal

university of health sciences

19H指数
138论文数
1.1K被引数
收录论文 21
发表时间
Expanding the clinical and molecular spectrum of NGLY1 deficiency: A multicenter cohort扩大NGLY1缺乏症的临床和分子谱:一项多中心队列研究
err2026-06-01
err0
PREAI
errYilmaz-Gumus, Emel; Kilavuz, Sebile; Demir, Senol; Aydogan, Ayca; Genc, Emine; Akar, Halil Tuna; Akbeyaz, Ismail Hakki; Cakar, Nafiye Emel; Er, Esra; Gulbahce, Aliye; Gunes, Hatice; Kardas, Fatih; Kilic, Mustafa; Teke-Kisa, Pelin; Kosukcu, Can; Onal, Hasan; Tas, Ibrahim; Turkdogan, Dilsad; Dursun, Ali; Ozturk-Hismi, Burcu
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Profiles of paediatric patients experiencing stroke-like episodes associated with mitochondrial disease线粒体疾病相关的卒中样发作患儿的临床特征
err2025-12-08
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errOAAI
errGülhan Karakaya Molla; Özlem Ünal Uzun; Hanım Babazade Agakisili; Emine Genç; Zümrüt Arslan Gülten; Tarık Yıldırım; Aydan Sezgin Ersoy; Belkıs Ak; Aliye Gülbahçe; Sevil Yıldız; Nafiye Emel Çakar; Meryem Karaca; Tanyel Zübarioğlu; Burcu Öztürk Hişmi; Şahin Erdöl; Hasan Önal; Bülent Kara; Gülden Fatma Gökçay
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Impact of Growth-promoting Therapies on Puberty, Growth, and Final Height in Classical 21-hydroxylase Deficiency生长促进疗法对经典型21-羟化酶缺乏症患者青春期、生长及最终身高的影响
err2025-12-01
err0
PREAI
errYavas Abali, Zehra; Yildiz, Melek; Abali, Saygin; Moniri, Ariorad; Bas, Firdevs; Onal, Hasan; Cilsaat, Gizem; Toksoy, Guven; Turan, Serap; Poyrazoglu, Sukran; Uyguner, Zehra Oya; Bundak, Ruveyde; Bereket, Abdullah; Darendeliler, Feyza; Guran, Tulay
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Developmental outcomes of children with biotinidase deficiency and the psychological state of their parents
err2025-03-10
err0
PREAI
errCelebi, Seda Bozduman; Akdag, Berhan; Cimbar, Hatice; Dag, Canan; Topal, Fatma; Noyan, Bilge; Onal, Hasan
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A novel graphene oxide-based fluorescence method for detection of urine glycosaminoglycans
err2024-03-06
err0
PREAI
errKoesoglu, Ceren Bakir; Dede, Sureyya; Karakus, Emine; Erdogmus, Ali; Keskin, Bahadir; Onal, Hasan
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Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency
err2021-04-08
err20
errOAAI
errYildiz, Melek; Isik, Emregul; Abali, Zehra Yavas; Keskin, Mehmet; Ozbek, Mehmet Nuri; Bas, Firdevs; Ucakturk, Seyit Ahmet; Buyukinan, Muammer; Onal, Hasan; Kara, Cengiz; Storbeck, Karl-Heinz; Darendeliler, Feyza; Cayir, Atilla; Unal, Edip; Anik, Ahmet; Demirbilek, Huseyin; Cetin, Tugba; Dursun, Fatma; Catli, Gonul; Turan, Serap; Falhammar, Henrik; Baris, Tugba; Yaman, Ali; Haklar, Goncagul; Bereket, Abdullah; Guran, Tulay
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The frequency of and factors affecting functional gastrointestinal disorders in infants that presented to tertiary care hospitals
err2021-04-03
err16
PREAI
errBeser, Omer Faruk; Cokugras, Fugen Cullu; Dogan, Guzide; Akgun, Ozlem; Elevli, Murat; Yilmazbas, Pinar; Ocal, Meric; Bayrak, Nevzat Aykut; Yamanel, Rabia Gonul Sezer; Bozaykut, Abdulkadir; Celtik, Coskun; Polat, Esra; Gerenli, Nelgin; Bozlak, Serdar; Civan, Hasret Ayyildiz; Saglam, Neslihan Ozkul; Hatipoglu, Sadik Sami; Ozgurhan, Gamze; Silistre, Eda Sunnetci; Solmaz, Burcu; Kutluk, Gunsel; Genc, Hamide Sevinc; Onal, Hasan; Usta, Ayse Merve; Urganci, Nafiye; Sahin, Ayse; Cam, Sebahat; Yildirim, Sema; Yildirim, Asilay; Vandenplas, Yvan
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Clinical Characteristics and Long-term Follow-of Patients with Diabetes Due To PTF1A Enhancer Mutations
err2020-09-07
err6
errOAAI
errDemirbilek, Huseyin; Cayir, Atilla; Flanagan, Sarah E.; Yildirim, Ruken; Kor, Yilmaz; Gurbuz, Fatih; Haliloglu, Belma; Yildiz, Melek; Baran, Riza Taner; Akbas, Emine Demet; Demiral, Meliha; Unal, Edip; Arslan, Gulcin; Vuralli, Dogus; Buyukyilmaz, Gonul; Al-Khawaga, Sara; Saeed, Amira; Al Maadheed, Maryam; Khalifa, Amel; Onal, Hasan; Yuksel, Bilgin; Ozbek, Mehmet Nuri; Bereket, Abdullah; Hattersley, Andrew T.; Hussain, Khalid; De Franco, Elisa
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Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases
err2020-01-17
err23
errOAAI
errGuran, Tulay; Kara, Cengiz; Yildiz, Melek; Bitkin, Eda C.; Haklar, Goncagul; Lin, Jen-Chieh; Keskin, Mehmet; Barnard, Lise; Anik, Ahmet; Catli, Gonul; Guven, Ayla; Kirel, Birgul; Tutunculer, Filiz; Onal, Hasan; Turan, Serap; Akcay, Teoman; Atay, Zeynep; Yilmaz, Gulay C.; Mamadova, Jamala; Akbarzade, Azad; Sirikci, Onder; Storbeck, Karl-Heinz; Baris, Tugba; Chung, Bon-Chu; Bereket, Abdullah
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Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross-sectional study
err2019-07-04
err7
errOAAI
errHatun, S.; Mutlu, G. Yesiltepe; Cinaz, P.; Turan, S.; Ekberzade, A.; Bereket, A.; Erbas, M. Y.; Akcay, T.; Onal, H.; Bolu, S.; Arslanoglu, I.; Doger, E.; Yilmaz, A. A.; Ucakturk, A.; Karabulut, G. S.; Tuhan, H. U.; Demir, K.; Erdeve, S. S.; Aycan, Z.; Nalbantoglu, O.; Kara, C.; Gungor, N.; Darendeliler, Feyza; Bundak, Ruveyde; Anik, Ahmet; Ucar, Ahmet; Cayir, Atilla; Ergur, Ayca Torel; Ozcabi, Bahar; Haliloglu, Belma; Ozkan, Behzat; Eklioglu, Beray Selver; Kirel, Birgul; Bezen, Digdem; Vuralli, Dogus; Unal, Edip; Sagsak, Elif; Bugrul, Fuat; Catli, Gonul; Korkmaz, Huseyin Anil; Ozbek, Mehmet Nuri; Tayfun, Meltem; Genens, Mikayir; Buyuk, Muammer; Hatipoglu, Nihal; Abali, Saygin; Kiremitci, Seniha; Curek, Yusuf; Siklar, Zeynep
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A nucleotide deletion and frame-shift cause analbuminemia in a Turkish family核苷酸缺失和移码导致土耳其家庭中的蛋白血症
err2016-01-01
err4
errOAAI
errCaridi, Gianluca; Gulec, Elif Yilmaz; Campagnoli, Monica; Lugani, Francesca; Onal, Hasan; Kilic, Duzgun; Galliano, Monica; Minchiotti, Lorenzo
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A novel mutation in the SLC25A15 gene in a Turkish patient with HHH syndrome: Functional analysis of the mutant protein
err2014-05-01
err22
errOAAI
errTunali, Nagehan Ersoy; Marobbio, Carlo M. T.; Tiryakioglu, N. Ozan; Punzi, Giuseppe; Saygili, Seha K.; Onal, Hasan; Palmieri, Ferdinando
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Is daily 400 IU of vitamin D supplementation appropriate for every country: a cross-sectional study
err2010-02-19
err22
PREAI
errOnal, Hasan; Adal, Erdal; Alpaslan, Secil; Ersen, Atilla; Aydin, Ahmet
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