Ahmet Cevdet Ceylan (A C Ceylan)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 8

Top Topics

Intellectual Disability

Botulinum Toxin

Top Venues

Journal of pediatric endocrinology & metabolism : JPEM

Molecular cytogenetics

The journal of gene medicine

Journal of intellectual disability research : JIDR

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

Publications

Ayşenur Engin Erdal, Burak Yürek, Oya Kıreker Köylü, Ahmet Cevdet Ceylan, Ayşegül Neşe Çıtak Kurt, Çiğdem Seher Kasapkara
Hereditary spastic paraplegia type 35 in a Turkish girl with fatty acid hydroxylase-associated neurodegeneration. Journal of pediatric endocrinology & metabolism : JPEM 37 (3) (2024)
Ayşenur Engin Erdal, Burak Yürek, Oya Kıreker Köylü, Ahmet Cevdet Ceylan, Ayşegül Neşe Çıtak Kurt, Çiğdem Seher Kasapkara
Hereditary spastic paraplegia type 35 in a Turkish girl with fatty acid hydroxylase-associated neurodegeneration. Journal of pediatric endocrinology & metabolism : JPEM (2024)
Ayşenur Engin Erdal, Burak Yürek, Oya Kıreker Köylü, Ahmet Cevdet Ceylan, Ayşegül Neşe Çıtak Kurt, Çiğdem Seher Kasapkara
Hereditary spastic paraplegia type 35 in a Turkish girl with fatty acid hydroxylase-associated neurodegeneration. Journal of pediatric endocrinology & metabolism : JPEM 37 (3) (2024)
Ayşenur Engin Erdal, Burak Yürek, Oya Kıreker Köylü, Ahmet Cevdet Ceylan, Ayşegül Neşe Çıtak Kurt, Çiğdem Seher Kasapkara
Hereditary spastic paraplegia type 35 in a Turkish girl with fatty acid hydroxylase-associated neurodegeneration. Journal of pediatric endocrinology & metabolism : JPEM 37 (3) (2024)
Ahmet Cevdet Ceylan, Oya Kireker Köylü, Hamit Özyürek, Eda Özaydin, Mehmet İlker Yön, Çiğdem Seher Kasapkara
Homozygous SLC20A2 mutations cause congenital CMV infection-like phenotype. Acta neurologica Belgica (2022)
Saide Betül Arslan Satılmış, Emin Emre Kurt, Ebru Perim Akçay, Ali Sazci, Ahmet Cevdet Ceylan
A novel missense mutation in the UBE2A gene causes intellectual disability in the large X-linked family. The journal of gene medicine 23 (2) (2021)
Ahmet Cevdet Ceylan, I Sahin, H B Erdem, G Kayhan, P O Simsek-Kiper, G E Utine, F Percin, K Boduroglu, M Alikasifoglu
An eight-case 1q21 region series: novel aberrations and clinical variability with new features. Journal of intellectual disability research : JIDR 63 (6) (2019)
Ahmet Cevdet Ceylan, Senol Citli, Haktan Bagis Erdem, Ibrahim Sahin, Elif Acar Arslan, Murat Erdogan
Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders. Molecular cytogenetics 11 (2018)