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Firdevs Baş

istanbul university

32H指数
344论文数
4.8K被引数
收录论文 48
发表时间
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Assessment of cardiometabolic risk using single point insulin sensitivity estimator (SPISE) in pediatric Bardet–Biedl Syndrome: a pilot study使用单点胰岛素敏感性估算器（SPISE）评估儿童巴德-比德尔综合征的心血管代谢风险：一项初步研究
errOrphanet Journal of Rare Diseases
IF3.5
err2026-08-06
err0
errOAAI
errTugce Kandemir; Melek Yildiz; Ummahan Tercan; Ozge Bayrak Demirel; Hasan Yanik; Volkan Karaman; Ayca Dilruba Aslanger; Aslı Derya Kardelen; Sukran Poyrazoglu; Feyza Darendeliler; Guven Toksoy; Firdevs Bas
err分享
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Near-final height outcomes in children with idiopathic short stature responsive to the IGF-1 generation test: a multicenter retrospective study of rhGH therapy特发性矮身材且对IGF-1生成试验有反应的儿童近最终身高结局：rhGH治疗的多中心回顾性研究
errBMC Endocrine Disorders
IF3.3
err2026-07-16
err0
errOAAI
errYavuz Özer; Hatice Ilgın Ruhi; Hande Turan; Melikşah Keskin; Sezgin Şahin; Veysel Nijat Baş; Zeynep Şıklar; Firdevs Baş; Zehra Aycan; Merih Berberoğlu; Büşra Hotaman; Ajlan Tükün; Feyza Darendeliler; Oya Ercan; Olcay Evliyaoğlu
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Gonadoblastoma with Dysgerminoma in a Virilized Adolescent with Karyotype 46,XX: A Case Report and Review of the Literature性腺母细胞瘤伴无性细胞瘤发生在性化发育的青少年（核型46,XX）：病例报告及文献综述
errJournal of Clinical Research in Pediatric Endocrinology
IF1.5
err2026-05-01
err0
PREAI
errKandemir, Tugce; Ozturan, Esin Karakilic; Dural, Ozlem; Aslanger, Ayca Dilruba; Balci, Elif Inan; Bayram, Aysel; Onder, Semen; Kardelen, Asli Derya; Yildiz, Melek; Poyrazoglu, Sukran; Bas, Firdevs; Darendeliler, Feyza
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A Rare Coexistence of Turner Syndrome and Mycosis Fungoides: A Case ReportTurner综合征与真菌样霉菌病罕见的共存：病例报告
errJournal of Clinical Research in Pediatric Endocrinology
IF1.5
err2026-05-01
err0
PREAI
errDemirel, Ozge Bayrak; Karakilic-Ozturan, Esin; Atci, Tugba; Sari, Sule Ozturk; Baykal, Can; Kardelen, Asli Derya; Yildiz, Melek; Poyrazoglu, Sukran; Bas, Firdevs; Darendeliler, Feyza
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Early-Onset Monogenic Obesity due to Leptin Receptor Deficiency: Fatal Outcome in Childhood in the Era of Precision Therapy由于瘦素受体缺陷导致的早发性单基因肥胖：精准治疗时代儿童期的致命结局
errHormone Research in Paediatrics
IF2.7
err2026-01-01
err0
PREAI
errTercan, Ummahan; Kandemir, Tugce; Kardelen, Asli Derya; Bas Ikizoglu, Nilay; Poyrazoglu, Sukran; Darendeliler, Feyza; Bas, Firdevs; Yildiz, Melek
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Olfactory Receptor Gene Deletions: A Novel Genetic Findings in Idiopathic Prepubertal Gynecomastia and Juvenile Macromastia嗅觉受体基因缺失：特发性青春期前男性乳房发育症和青少年巨乳症的全新遗传发现
errHORMONE RESEARCH IN PAEDIATRICS
IF2.7
err2025-11-01
err0
PREAI
errBas, Firdevs; Karaman, Birsen; Kardelen, Asli Derya; Heidargholizadeh, Somayyeh; Najafli, Adam; Toksoy, Guven; Koc, Cansu; Poyrazoglu, Sukran; Yildiz, Melek; Uyguner, Zehra Oya; Basaran, Seher; Darendeliler, Feyza
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The Outcome of Regular Well-Child Follow-Up From Birth on Adolescent Well-Being
errCHILD CARE HEALTH AND DEVELOPMENT
IF2
err2025-10-26
err0
PREAI
errAksakal, Melike Tugrul; Askan, Oyku Ozboru; Kayi, Alev Bakir; Sahin, Aylin Yetim; Keskindemirci, Gonca; Kuleli, Osman; Parildar, Hilal; Bas, Firdevs; Gokcay, Gulbin
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Long-term follow-up of growth and puberty in 3-M syndrome: effects of growth hormone therapy and response variability3-M综合征长期随访的生长和青春期发育：生长激素治疗的效果及反应变异性
errEndocrine
IF2.9
err2025-09-20
err0
PREAI
errAyse Pinar Ozturk; Ayca Dilruba Aslanger; Umut Altunoglu; Cagri Gulec; Esin Karakilic Ozturan; Volkan Karaman; Elif Yilmaz Gulec; Alper Gezdirici; Gozde Yesil; Guven Toksoy; Melek Yildiz; Sukran Poyrazoglu; Firdevs Bas; Zehra Oya Uyguner; Hulya Kayserili; Feyza Darendeliler
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Comprehensive clinical and molecular characterization with long-term outcomes in 40 patients with congenital hyperinsulinism40例先天性高胰岛素血症患者的全面临床与分子特征分析及长期预后
errENDOCRINE
IF2.9
err2025-05-18
err0
PREAI
errAbali, Zehra Yavas; Bas, Firdevs; Houghton, Jayne A. L.; Abali, Saygin; Ozturan, Esin Karakilic; Gulec, Cagri; Aslanger, Ayca Dilruba; Kandemir, Tugce; Durmaz, Durmus; Yucesoy, Mehmet Akif; Flanagan, Sarah E.; Poyrazoglu, Sukran; Bundak, Ruveyde; Darendeliler, Feyza
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Investigation of dysmenorrhea in adolescent girls with familial Mediterranean fever: a comparative study with healthy controls
errEUROPEAN JOURNAL OF PEDIATRICS
IF2.6
err2025-02-19
err0
errOAAI
errDemirkan, Fatma Gul; Sahin, Aylin Yetim; Cakmak, Figen; Akguen, Ozlem; Guliyeva, Vafa; Aksakal, Melike Zeynep Tugrul; Bas, Firdevs; Ayaz, Nuray Aktay
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Effect of obesity and NAFLD on leukocyte telomere length and hTERT gene MNS16A VNTR variant
errSCIENTIFIC REPORTS
IF3.9
err2024-10-23
err0
errOAAI
errKandemir, Ibrahim; Sahin, Aylin Yetim; Oyaci, Yasemin; Khudiyeva, Shahri; Sahin, Memduh; Aksakal, Melike Tugrul; Pehlivan, Mustafa; Bas, Firdevs; Pehlivan, Sacide
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17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
errENDOCRINE
IF2.9
err2024-07-17
err2
errOAAI
errSiklar, Zeynep; Camtosun, Emine; Bolu, Semih; Yildiz, Melek; Akinci, Aysehan; Bas, Firdevs; Dundar, Ismail; Bestas, Asli; Unal, Edip; Kocaay, Pinar; Guran, Tulay; Buyukyilmaz, Gonul; Ugurlu, Aylin Kilinc; Tosun, Busra Gurpinar; Turan, Ihsan; Kurnaz, Erdal; Yuksel, Bilgin; Turkkahraman, Doga; Cayir, Atilla; Celmeli, Gamze; Gonc, E. Nazli; Eklioglu, Beray Selver; Cetinkaya, Semra; Yilmaz, Seniha Kiremitci; Atabek, Mehmet Emre; Buyukinan, Muammer; Arslan, Emrullah; Mengen, Eda; Cakir, Esra Deniz Papatya; Karaoglan, Murat; Hatipoglu, Nihal; Orbak, Zerrin; Ucar, Ahmet; Akyurek, Nesibe; Akbas, Emine Demet; Isik, Emregul; Kaygusuz, Sare Betul; Sutcu, Zumrut Kocabey; Seymen, Gulcan; Berberoglu, Merih
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Evaluation of the ability of insulin resistance and lipid-related indices to predict the presence of NAFLD in obese adolescents
errLIPIDS IN HEALTH AND DISEASE
IF4.2
err2024-07-02
err4
errOAAI
errYetim, Aylin; Sahin, Memduh; Kandemir, Ibrahim; Bulakci, Betul; Aksakal, Melike Tugrul; Karapinar, Edanur; Sever, Hayrettin; Bas, Firdevs
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Novel variants ensued genomic imprinting in familial central precocious puberty
errJOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
IF3.5
err2024-02-17
err2
errOAAI
errKaraman, V.; Karakilic-Ozturan, E.; Poyrazoglu, S.; Gelmez, M. Y.; Bas, F.; Darendeliler, F.; Uyguner, Z. O.
err分享
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Ovarian and paraovarian adrenal rest tumors are not uncommon in gonadectomy materials of historical congenital adrenal hyperplasia cases in childhood
errEUROPEAN JOURNAL OF ENDOCRINOLOGY
IF5.2
err2022-06-01
err2
errOAAI
errYildiz, Melek; Bayram, Aysel; Bas, Firdevs; Karaman, Volkan; Toksoy, Guven; Poyrazoglu, Sukran; Soysal, Feryal Gun; Onder, Semen; Uyguner, Zehra Oya; Darendeliler, Feyza
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Pelvic and breast ultrasound abnormalities and associated metabolic disturbances in girls with premature pubarche due to adrenarche
errCLINICAL ENDOCRINOLOGY
IF2.4
err2021-12-27
err3
errOAAI
errAydin, Banu K.; Kadioglu, Alev; Kaya, Gamze A.; Devecioglu, Esra; Bas, Firdevs; Poyrazoglu, Sukran; Gokcay, Gulbin; Darendeliler, Feyza
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Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency
errJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
IF5.1
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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Growth and relationship of phenotypic characteristics with gonadal pathology and tumour risk in patients with 45, X/46, XY mosaicism45，X/46，XY嵌合体患者的生长及其表型特征与性腺病理和肿瘤风险的关系
errCLINICAL ENDOCRINOLOGY
IF2.4
err2021-02-17
err7
PREAI
errPoyrazoglu, Sukran; Bas, Firdevs; Karaman, Birsen; Yildiz, Melek; Basaran, Seher; Darendeliler, Feyza
err分享
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Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease
errJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
IF5.1
err2019-05-01
err53
errOAAI
errJolly, Angad; Bayram, Yavuz; Turan, Serap; Aycan, Zehra; Tos, Tulay; Abali, Zehra Yavas; Hacihamdioglu, Bulent; Akdemir, Zeynep Hande Coban; Hijazi, Hadia; Bas, Serpil; Atay, Zeynep; Guran, Tulay; Abali, Saygin; Bas, Firdevs; Darendeliler, Feyza; Colombo, Roberto; Barakat, Tahsin Stefan; Rinne, Tuula; White, Janson J.; Yesil, Gozde; Gezdirici, Alper; Gulec, Elif Yilmaz; Karaca, Ender; Pehlivan, Davut; Jhangiani, Shalini N.; Muzny, Donna M.; Poyrazoglu, Sukran; Bereket, Abdullah; Gibbs, Richard A.; Posey, Jennifer E.; Lupski, James R.
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A novel 3′ untranslated region mutation in the SLC29A3 gene associated with pigmentary hypertrichosis and non-autoimmune insulin-dependent diabetes mellitus syndrome
errPEDIATRIC DIABETES
IF5.6
err2019-04-02
err5
errOAAI
errRiachi, Melissa; Bas, Firdevs; Darendeliler, Feyza; Hussain, Khalid
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研究方向

暂时未获取到该数据
合作学者
合作期刊
R
Richard A. Gibbs
H 指数: 190 · 论文数: 1.3K
J
James R. Lupski
H 指数: 144 · 论文数: 1.1K
M
Maria I. New
H 指数: 96 · 论文数: 785
S
Shalini N. Jhangiani
H 指数: 73 · 论文数: 260
H
Hülya Kayserili
H 指数: 71 · 论文数: 350
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