Mesut Gungor (Mesut Güngör)

Publication Activity (10 Years)

Years Active: 2020-2022
Publications (10 Years): 7

Top Topics

Intellectual Disability

Botulinum Toxin

Top Venues

Journal of pediatric genetics

Rheumatology international

Neuropediatrics

Pediatrics international : official journal of the Japan Pediatric Society

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

Publications

Mesut Gungor, Muhammet Akif Guler, Yuksel Sumeyra Karagoz
Management and behavior-modifying recommendation effects in childhood headache. Pediatrics international : official journal of the Japan Pediatric Society (2022)
Mesut Gungor, Evren Demirsoy, Ayfer Sakarya Güneş, Yonca Anık, Bülent Kara
Recurrent Blistering Skin Lesions and Reversible Monocular Abducens Paralysis in a Patient with CD59 Deficiency. Neuropediatrics 53 (2) (2022)
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)