Scientific Publication
Distinctive pattern of temporal atrophy in patients with frontotemporal dementia and the I383V variant in TARDBP
JOURNAL OF NEUROLOGY, NEUROSURGERY & PSYCHIATRY, 2021
Merel O. Mol, Sebastiaan W.R. Nijmeijer, Jeroen G. J. van Rooij, Resie M. L. van Spaendonk, Yolande A. L. Pijnenburg, Sven J. van der Lee, Rick van Minkelen, Laura Donker Kaat, Annemieke J. M. Rozemuller, Mark R. Janse van Mantgem, Wouter van Rheenen, Michael A. van Es, Jan H. Veldink, Frederic A. M. Hennekam, Meike Vernooij, John C. van Swieten, Petra E. Cohn-Hokke, Harro Seelaar, Elise G.P. Dopper
January 15, 2021
- This study examines the genetic cause of frontotemporal dementiaand finds a distinctive pattern of temporal atrophy in patients with one specific gene-variant.
- In this study, Quantib® ND was used for quantitative assessment of volume loss across lobar brain regions.
