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Handbook of Clinical Neurology|August 13, 2013
Recessively transmitted predominantly motor neuropathiesYeşim Parman, Esra BattaloğluBalkan Medical Journal|March 25, 2022
Clinical and Genetic Survey for Charcot-Marie-Tooth Neuropathy Based on the Findings in Turkey, a Country with a High Rate of Consanguineous MarriagesAyşe Candayan, Yeşim Parman, Esra BattaloğluJournal of Pediatric Hematology/Oncology|September 23, 2009
Low dose vincristine-induced severe polyneuropathy in a Hodgkin lymphoma patient: a case report (vincristine-induced severe polyneuropathy)Timucin Cil, Abdullah Altintas, Yusuf Tamam, et al.Neurologia I Neurochirurgia Polska|April 4, 2020
Clinical and genetic aspects of hereditary spastic paraplegia in patients from TurkeyNihan H Akçakaya, Burçak Özeş Ak, Michael A Gonzalez, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 20, 2023
A novel homozygous loss-of-function variant in SOD1 causing progressive spastic tetraplegia and axial hypotoniaArman Çakar, Emre Pekbilir, Serdar Ceylaner, et al.Neurogenetics|November 2, 2019
The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotypeAyşe Candayan, Gulshan Yunisova, Arman Çakar, et al.Acta Neurologica Scandinavica|February 7, 2022
Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorderArman Çakar, Meltem İnci, Ayşe Nur Özdağ Acarlı, et al.Acta Neurologica Belgica|June 8, 2021
Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical featuresArman Çakar, Erdi Şahin, Seden Tezel, et al.Neurology. Clinical Practice|April 12, 2021
Selective Bilateral Vestibular Neuropathy in a Turkish CMT1B Family With a Novel MPZ MutationGülden Akdal, Koray Koçoğlu, Elçin Bora, et al.Neurology. Genetics|September 3, 2021
Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish CohortAyşe Candayan, Arman Çakar, Gulshan Yunisova, et al.Pageof 2