Tayfun Çinleti (Tayfun Cinleti)

Publication Activity (10 Years)

Years Active: 2022-2023
Publications (10 Years): 2

Top Topics

Genome Wide Identification

Top Venues

Acta neurologica Belgica

Journal of pediatric endocrinology & metabolism : JPEM

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

Publications

Özlem Özsoy, Tayfun Çinleti, Çağatay Günay, Gamze Sarikaya Uzan, Özlem Giray Bozkaya, Ahmet Okay Çağlayan, A Semra Hiz, Uluç Yaş
Genetic, serological and clinical evaluation of childhood myasthenia syndromes- single center subgroup analysis experience in Turkey. Acta neurologica Belgica (2023)
Gizem Yildiz, Meral Torun Bayram, Tayfun Çinleti, Altug Koc, Alper Soylu, Salih Kavukcu
Late onset Bartter syndrome: Bartter syndrome type 2 presenting with isolated nephrocalcinosis and high parathyroid hormone levels mimicking primary hyperparathyroidism. Journal of pediatric endocrinology & metabolism : JPEM 35 (10) (2022)