DPAGT1-CDG: Report of Two New Pediatric Patients and Brief Review of the LiteratureÖzlem Özsoy, Semra Hız Kurul, Uluç Yiş et al.|Molecular Syndromology|2023Cited by 6
Genetic, serological and clinical evaluation of childhood myasthenia syndromes- single center subgroup analysis experience in TurkeyÖzlem Özsoy, Uluç Yiş, Gamze Sarıkaya Uzan et al.|Acta Neurologica Belgica|2023Cited by 4
Molecular Diagnosis of Limb-Girdle Muscular Dystrophy Using Next-Generation Sequencing PanelsGamze Sarıkaya Uzan, Uluç Yiş, Ceren Yılmaz Uzman et al.|Molecular Syndromology|2023Cited by 4
A novel DOCK7 variant as a rare reason for epileptic encephalopathy, cortical blindness, dysmorphic features: A case report and brief review of the literatureÖzlem Özsoy, Uluç Yiş, Çağatay Günay et al.|Neurology Asia|2023Cited by 0
Phenotypic comparison of a novel variant (p.P164R) and A founder mutation (c.748+1G>A) in Warburg Micro syndromeTayfun Çinleti, Özlem Giray Bozkaya, Uluç Yiş et al.|Neurology Asia|2023Cited by 0