Bulent Kara (Bülent Kara)

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 6

Top Topics

Patient Reported

Intellectual Disability

Ejection Fraction

Top Venues

Journal of pediatric genetics

Rheumatology international

Neuropediatrics

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

Publications

Çağatay Günay, Duygu Aykol, Özlem Özsoy, Ece Sönmezler, Yaren Sena Hanci, Bulent Kara, Deniz Akkoyunlu Sünnetçi, Naci Cine, Adnan Deniz, Tolgahan Özer, Cemile Büşra Ölçülü, Özlem Yilmaz, Seda Kanmaz, Sanem Yilmaz, Hasan Tekgül, Nihal Yildiz, Elif Acar Arslan, Ali Cansu, Nihal Olgaç Dündar, Fatma Kusgoz, Elif Didinmez, Pinar Gencpinar, Tuğçe Aksu Uzunhan, Biray Ertürk, Alper Gezdirici, Akif Ayaz, Akgün Ölmez, Müge Ayanoğlu, Ayşe Fahriye Tosun, Yasemin Topçu, Betül Kılıç, Kursad Aydin, Ezgi Çağlar, Özlem Ersoy Kosvali, Cetin Okuyaz, Şeyda Besen, Leman Tekin Orgun, İlknur Erol, Deniz Yüksel, Abdullah Sezer, Ergin Atasoy, Ülkühan Öztoprak, Serdal Güngör, Bilge Ozgor, Meral Karadağ, Cengiz Dilber, Bahtiyar Şahinoğlu, Emek Uyur Yalçın, Nilüfer Eldes Hacifazlioglu, Ahmet Yaramiş, Pinar Edem, Hande Gazeteci Tekin, Ünsal Yilmaz, Aycan Ünalp, Sevim Turay, Didem Biçer, Gülen Gül Mert, İpek Dokurel Çetin, Serkan Kırık, Gülten Öztürk, Yasemin Karal, Aslıhan Sanri, Ayşe Aksoy, Muzaffer Polat, Nezir Özgün, Didem Soydemir, Gamze Sarikaya Uzan, Döndü Ülker Üstebay, Ayşen Gök, Mehmet Can Yeşilmen, Uluç Yaş, Gökhan Karakülah, Ahmet Bursali, Yavuz Oktay, A Semra Hiz
Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study. Neuropediatrics (2023)
Adnan Deniz, Sinan Çomu, Mesut Gungor, Yonca Anık, Bulent Kara
Compound Heterozygous ROBO3 Mutation in Two Siblings Presenting with Horizontal Gaze Palsy without Scoliosis: Case-Based Review. Journal of pediatric genetics 13 (2) (2021)
Sema Aylan Gelen, Bulent Kara, Isil Eser Şimsek, Mesut Gungor, Emine Zengin, Nazan Sarper
Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5 . Journal of pediatric genetics 13 (1) (2021)
Sema Aylan Gelen, Bulent Kara, Isil Eser Şimsek, Mesut Gungor, Emine Zengin, Nazan Sarper
Autoimmune Hemolytic Anemia Due to Spondyloenchondrodysplasia with Spastic Paraparesis and Intracranial Calcification due to Mutation in ACP5 . Journal of pediatric genetics 13 (1) (2021)
Adnan Deniz, Sinan Çomu, Mesut Gungor, Yonca Anık, Bulent Kara
Compound Heterozygous ROBO3 Mutation in Two Siblings Presenting with Horizontal Gaze Palsy without Scoliosis: Case-Based Review. Journal of pediatric genetics 13 (2) (2021)
Bulent Kara, Zelal Ekinci, Sezgin Şahin, Mesut Gungor, Ayfer Sakarya Gunes, Kübra Oztürk, Amra Adrovic, Ayşe Cefle, Murat Inanç, Ahmet Gül, Ozgur Kasapcopur
Monogenic lupus due to spondyloenchondrodysplasia with spastic paraparesis and intracranial calcification: case-based review. Rheumatology international 40 (11) (2020)