Ayşe Candayan
Bogaziçi Üniversitesi
H-index: 5
Asia-Turkey
Top articles of Ayşe Candayan
Distinct Genetic Distribution of Distal Hereditary Motor Neuropathy in Turkey: A Single Centre Experience (P2-11.009)
2024/4/14
Genotypic And Phenotypic Features of Patients with GJB1 Mutations: Single Center Experience (P11-8.003)
2023/4/25
Phenotypic and genetic heterogeneity of adult patients with hereditary spastic paraplegia from Serbia
Cells
2022/9/8
Ayşe Candayan
H-Index: 3
Nikola Momčilović
H-Index: 5
Igor Petrović
H-Index: 1
Albena Jordanova
H-Index: 36
Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features
Acta Neurologica Belgica
2022/8
Single Center Experience of SORD Neuropathy in Turkey (P1-1. Virtual)
Neurology
2022/5/3
Central Nervous System Involvement in HINT1 Neuropathy: An Overlooked Phenotypical Feature?(P8-13.001)
2022/5/3
Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder
Acta Neurologica Scandinavica
2022/5
Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity
The American Journal of Human Genetics
2022/3/3
Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort (vol 7, e621, 2021)
NEUROLOGY-GENETICS
2022/2/1
Clinical and genetic survey for Charcot-Marie-Tooth neuropathy based on the findings in Turkey, a country with a high rate of consanguineous marriages
Balkan Medical Journal
2022/1
Ayşe Candayan
H-Index: 3
Esra Battaloğlu
H-Index: 16
Investigation of novel recessive causative genes and gene/allele frequency for CMT disease in Turkey
2021
Ayşe Candayan
H-Index: 3
Genotypic and phenotypic features of mutations in the HINT1 gene among Turkish patients with hereditary axonal neuropathy
2021
The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype
neurogenetics
2020/1
