Gizem Ürel-Demir (Gizem Urel-Demir, Gizem Urel Demir)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 6

Top Topics

Extracorporeal Membrane Oxygenation

Dna Methylation

Newly Diagnosed

Top Venues

American journal of medical genetics. Part A

Journal of human genetics

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

Publications

Ezgi Burgac, İrem Kaplan, Burcu Köseci, Esra Kara, Deniz Kor, Fatma Derya Bulut, Anıl Atmıs, Ferhat Can Piskin, Sevcan Tuğ Bozdoğan, Gizem Ürel-Demir, Faruk Incecik, Halise Neslihan Onenli Mungan
Early diagnostic clues of mucolipidosis type II: Significance of radiological findings. American journal of medical genetics. Part A 194 (6) (2024)
Ezgi Burgac, İrem Kaplan, Burcu Köseci, Esra Kara, Deniz Kor, Fatma Derya Bulut, Anıl Atmıs, Ferhat Can Piskin, Sevcan Tuğ Bozdoğan, Gizem Ürel-Demir, Faruk Incecik, Halise Neslihan Onenli Mungan
Early diagnostic clues of mucolipidosis type II: Significance of radiological findings. American journal of medical genetics. Part A 194 (6) (2024)
Ezgi Burgac, İrem Kaplan, Burcu Köseci, Esra Kara, Deniz Kor, Fatma Derya Bulut, Anıl Atmıs, Ferhat Can Piskin, Sevcan Tuğ Bozdoğan, Gizem Ürel-Demir, Faruk Incecik, Halise Neslihan Onenli Mungan
Early diagnostic clues of mucolipidosis type II: Significance of radiological findings. American journal of medical genetics. Part A (2024)
Akçahan Akalın, Ercan Ayaz, Merve Soğukpınar, Enise Avci Durmusalioglu, Gizem Ürel-Demir, Adalet Elcin Yildiz, Tahir Atik, Nursel H Elcioglu, Gülen Eda Utine, Pelin Özlem Şimsek Kiper
Further defining the molecular spectrum and long-term follow-up of 17 patients with Dyggve-Melchior-Clausen and Smith-McCort dysplasia type 2. American journal of medical genetics. Part A (2024)
Pelin Özlem Şimsek Kiper, Gizem Ürel-Demir, Ekim Z Taskiran, Umut Ece Arslan, Banu Nur, Ercan Mihci, Mithat Haliloglu, Yasemin Alanay, Gulen Eda Utine, Koray Boduroglu
Further defining the clinical and molecular spectrum of acromesomelic dysplasia type maroteaux: a Turkish tertiary center experience. Journal of human genetics 66 (6) (2020)
Gizem Ürel-Demir, Pelin Ozlem Simsek-Kiper, Özlem Akgün-Doğan, Rahşan Göçmen, Zheng Wang, Naomichi Matsumoto, Noriko Miyake, Gülen Eda Utine, Gen Nishimura, Shiro Ikegawa, Koray Boduroglu
Further expansion of the mutational spectrum of spondylo-meta-epiphyseal dysplasia with abnormal calcification. Journal of human genetics 63 (9) (2018)