Zehra Yavaş Abalı (Zehra Yavas Abalı, Zehra Yavas Abali)

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 6

Top Topics

Top Venues

Journal of clinical research in pediatric endocrinology

Hormones (Athens, Greece)

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Esin Karakılıc Ozturan, Umut Altunoglu, Ayse Pinar Ozturk, Asli Derya Kardelen Al, Zehra Yavaş Abalı, Sahin Avci, Bernd Wollnik, Şükran Poyrazoğlu, Firdevs Baş, Zehra Oya Uyguner, Hülya Kayserili, Feyza Darendelıler
Evaluation of growth, puberty, osteoporosis, and the response to long-term bisphosphonate therapy in four patients with osteoporosis-pseudoglioma syndrome. American journal of medical genetics. Part A 188 (7) (2022)
Rüveyde Bundak, Zehra Yavaş Abalı, Andrzej Furman, Feyza Darendelıler, Emine Gülbin Gökçay, Firdevs Baş, Hülya Günöz, Olcay Neyzi
Comparison of National Growth Standards for Turkish Infants and Children with World Health Organization Growth Standards Journal of clinical research in pediatric endocrinology 14 (2) (2022)
Neşe Akcan, Zehra Oya Uyguner, Firdevs Baş, Umut Altunoglu, Güven Toksoy, Birsen Karaman, Sahin Avci, Zehra Yavaş Abalı, Şükran Poyrazoğlu, Agharza Aghayev, Volkan Karaman, Rüveyde Bundak, Seher Başaran, Feyza Darendelıler
Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD Journal of clinical research in pediatric endocrinology 14 (2) (2022)
Asli Derya Kardelen Al, Manolya Kara, Dilek Güller, Esin Karakılıc Ozturan, Zehra Yavaş Abalı, Serdar Ceylaner, Ayça Kiykim, Serdar Cantez, Selda Hancerlı Torun, Şükran Poyrazoğlu, Firdevs Baş, Feyza Darendelıler
LRBA deficiency: a rare cause of type 1 diabetes, colitis, and severe immunodeficiency. Hormones (Athens, Greece) 20 (2) (2020)
Firdevs Baş, Zehra Yavaş Abalı, Güven Toksoy, Şükran Poyrazoğlu, Rüveyde Bundak, Çağrı Güleç, Zehra Oya Uyguner, Feyza Darendeliler
Precocious or early puberty in patients with combined pituitary hormone deficiency due to POU1F1 gene mutation: case report and review of possible mechanisms. Hormones (Athens, Greece) 17 (4) (2018)
Şükran Poyrazoğlu, Rüveyde Bundak, Zehra Yavaş Abalı, Hasan Önal, Sevil Sarıkaya, Abdurrahman Akgün, Serpil Baş, Saygın Abalı, Abdullah Bereket, Erdal Eren, Ömer Tarım, Ayla Güven, Metin Yıldız, Derya Karaman Aksakal, Ayşegül Yüksel, Gülcan Seymen-Karabulut, Şükrü Hatun, İlker Tolga Özgen, Yaşar Cesur, Mehmet Azizoğlu, Emine Dilek, Filiz Tütüncüler Kökenli, Esra Deniz Papatya Çakır, Mesut Dursun, Saadet Olcay Evliyaoglu, Songül Karadeniz, Fatma Dursun, Semih Bolu, Ilknur Arslanoglu, Gül Yeşiltepe Mutlu, Heves Kirmizibekmez, Şükriye Pınar İşgüven, Ala Üstyol, Servet Erdal Adal, Ahmet Uçar, Ayse Nurcan Cebeci, Diğdem Bezen, Çiğdem Binay, Serap Semiz, Hüseyin Anil Korkmaz, Nihal Memioğlu, Elif Sağsak, Havva Nur Peltek Kendirci, Melek Yıldız, Teoman Akçay, Serap Turan, Tülay Güran, Zeynep Atay, Neşe Akcan, Filiz Mine Çizmecioğlu-Jones, Oya Ercan, Aydilek Dagdeviren Cakir, Firdevs Baş, Halim Issever, Feyza Darendelıler
Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey Journal of clinical research in pediatric endocrinology 10 (4) (2018)