Sevim Erdem-Özdamar

Myophosphorylase (PYGM) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease

U. Giger, Y. Parman, Hüseyin Demirci, 2017, Neuromuscular Disorders.

Overexpression of amyloid beta precursor protein enhances expression and secretion of ST6Gal1 in C2C12 myogenic cell line

Sevim Erdem-Özdamar, B. Balci-Hayta, P. Dinçer, 2011, Cell biology international.

Spinal muscular atrophy type III: Molecular genetic characterization of Turkish patients.

C. Bekircan-Kurt, Sevim Erdem-Özdamar, G. Bora-Tatar, 2015, European journal of medical genetics.

Transcript levels of plastin 3 and neuritin 1 modifier genes in spinal muscular atrophy siblings

H. Topaloglu, Sevim Erdem-Özdamar, D. Dayangaç-Erden, 2017, Pediatrics international : official journal of the Japan Pediatric Society.

Neuropathic Pain Frequency in Neurology Outpatients: A Multicenter Study

B. Uludaǧ, M. Akalın, C. Boz, 2021, Noro psikiyatri arsivi.

New mutations and genotype–phenotype correlation in late-onset Pompe patients

E. Tan, E. Saka, C. Bekircan-Kurt, 2017, Acta Neurologica Belgica.