Fatih Tepgeç

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

Hülya Uluğut Erkoyun, Sven J. van der Lee, Bas Nijmeijer et al. · Journal of Alzheimer s Disease · 2021 · 26 citations · Full text

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

Emel Oğuz Akarsu, Pınar Tektürk, Fatih Tepgeç et al. · Seizure · 2016 · 15 citations · Full text

Rare Diseases, Progressive Myoclonic Epilepsy, Ophthalmology +13

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

Emel Köseoğlu, Fatih Tepgeç, Mehmet Fatih Yetkin et al. · Nöro Psikiyatri Arşivi · 2017 · 11 citations

<i>TREM2</i> variants as a possible cause of frontotemporal dementia with distinct neuroimaging features

Bedia Samancı, Özlem Gelişin, Fatih Tepgeç et al. · European Journal of Neurology · 2021 · 10 citations