Sahin Avci (Şahin Avcı)

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 6

Top Topics

Intellectual Disability

Temporal Lobe Epilepsy

Top Venues

Epileptic disorders : international epilepsy journal with videotape

American journal of medical genetics. Part A

Journal of clinical research in pediatric endocrinology

Clinical genetics

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

Publications

Selen Üçem, Sahin Avci, Candan GÜrses
A genetic cause for intractable seizures: Atypical Gaucher disease with a novel pathological variant. Epileptic disorders : international epilepsy journal with videotape (2024)
Selen Üçem, Sahin Avci, Candan GÜrses
A genetic cause for intractable seizures: Atypical Gaucher disease with a novel pathological variant. Epileptic disorders : international epilepsy journal with videotape 26 (3) (2024)
Ece Çepni, Esra Börklü, Sahin Avci, Tuğba Kalaycı, Serpil Eraslan, Hülya Kayserili
Revisiting TOP2B-related phenotypes: Three new cases and literature review. Clinical genetics (2023)
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)
Tuğba Kalaycı, Umut Altunoglu, Aytul Çorbacioglu Esmer, Sahin Avci, Tugba Sarac Sivrikoz, Birsen Karaman, İbrahim Kalelioğlu, Recep Has, Zehra Oya Uyguner, Atıl Yüksel, Seher Başaran, Hülya Kayserili
Fetal skeletal dysplasia cohort of a single tertiary referral center in Istanbul, Turkey. American journal of medical genetics. Part A (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)