Stayko Sarafov

Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of<i>TTR</i>gene mutations*

Isabel Conceição, Thibaud Damy, Manuel Jesús Romero-Jiménez et al. · Amyloid · 2019 · 180 citations · Full text

Genetic Testing, Genetic Epidemiology, Diagnosis +21

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Julie van der Zee, Tim Van Langenhove, Gábor G. Kovács et al. · Acta Neuropathologica · 2014 · 113 citations · Full text

<i>TBK1</i> Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde et al. · Human Mutation · 2016 · 102 citations · Full text

Neurogenomics, Neurological Disorder, Genetics +28

Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients

Lubina Dillen, Tim Van Langenhove, Sebastiaan Engelborghs et al. · Neurobiology of Aging · 2013 · 40 citations

Genetic Disorder, Genetics, Genetic Epidemiology +12

Peripheral nerve ultrasonography in patients with transthyretin amyloidosis

Simon Podnar, Stayko Sarafov, Ivailo Tournev et al. · Clinical Neurophysiology · 2017 · 39 citations

Alzheimer's Disease, Engineering, Peripheral Nerve Ultrasonography +6