Fatih Tepgec

Frequency of frontotemporal dementia-related gene variants in Turkey

H. Gurvit, M. Emre, S. Artan, 2021, Neurobiology of Aging.

Clinical and molecular genetic findings of hereditary Parkinson's patients from Turkey.

M. Emre, H. Hanagasi, B. Bilgiç, 2021, Parkinsonism & Related Disorders.

TREM2 variants as a possible cause of frontotemporal dementia with distinct neuroimaging features

J. Hardy, R. Guerreiro, M. Emre, 2021, European journal of neurology.

Nasu Hakola Disease: A Rare Cause of Dementia and Cystic Bone Lesions, Report of a New Turkish Family.

H. Hanagasi, O. Uyguner, M. Yetkin, 2017, Noro psikiyatri arsivi.

A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer’s disease

H. Gurvit, H. Hanagasi, B. Bilgiç, 2021, Neurological Sciences.

Eyelid myoclonic status epilepticus: A rare phenotype in spinal muscular atrophy with progressive myoclonic epilepsy associated with ASAH1 gene mutation

B. Baykan, P. Tekturk, Z. Uyguner, 2016, Seizure.

The Right Temporal Variant of Frontotemporal Dementia Is Not Genetically Sporadic: A Case Series

W. M. van der Flier, P. Scheltens, F. Barkhof, 2021, Journal of Alzheimer's disease : JAD.

Functional Connectivity Analysis in Heterozygous Glucocerebrosidase Mutation Carriers.

T. Demiralp, H. Gurvit, M. Emre, 2021, Journal of Parkinson's disease.