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White matter hyperintensities are seen only inGRNmutation carriers in the GENFI cohort.
Carole H Sudre, Martina Bocchetta, David Cash, David L Thomas, Ione Woollacott, Katrina M Dick, John van Swieten, Barbara Borroni, Daniela Galimberti, Mario Masellis, Maria Carmela Tartaglia, James B Rowe, Caroline Graff, Fabrizio Tagliavini, Giovanni Frisoni, Robert Laforce, Elizabeth Finger, Alexandre de Mendonça, Sandro Sorbi, Sébastien Ourselin, M Jorge Cardoso, Jonathan D Rohrer, GENFI Genetic FTD Initiative
Nov 23, 2017
Genetic frontotemporal dementia is most commonly caused by mutations in the progranulin(GRN), microtubule-associated protein tau (MAPT)and chromosome 9 open reading frame 72(C9orf72) genes. Previous small studies have reported...
CI Confidence interval FTD Frontotemporal dementia IQR Inter Quartile Range PS Presymptomatic S Symptomatic TIV Total Intracranial volume WMH White matter hyperintensity Adult Aged C9orf72 Protein Cohort Studies Female frontotemporal dementia Humans Intercellular Signaling Peptides and Proteins Magnetic Resonance Imaging Male Middle Aged white matter tau Proteins