Experimental Neurobiology Unit

Stratifying the presymptomatic phase of genetic frontotemporal dementia by serum NfL and pNfH : a longitudinal multicentre study

Source
Annals of neurology - ISSN 1531-8249-91:1 (2022) p. 33-47
Author(s)
    Carlo Wilke, Selina Reich, John C. van Swieten, Barbara Borroni, Raquel Sanchez-Valle, Fermin Moreno, Robert Laforce, Caroline Graff, Daniela Galimberti, James B. Rowe, Mario Masellis, Maria Carmela Tartaglia, Elizabeth Finger, Rik Vandenberghe, Alexandre de Mendonça, Fabrizio Tagliavini, Isabel Santana, Simon Ducharme, Chris R. Butler, Alexander Gerhard, Johannes Levin, Adrian Danek, Markus Otto, Giovanni Frisoni, Roberta Ghidoni, Sandro Sorbi, Martina Bocchetta, Emily Todd, Jens Kuhle, Christian Barro, Rose Bruffaerts, Jonathan D. Rohrer, Matthis Synofzik
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A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study.

Source
JAMA neurology - ISSN 1750-1326-16:1 (2021) p.
Author(s)
    Sofia Bergström, Linn Öijerstedt, Julia Remnestål, Jennie Olofsson, Abbe Ullgren, Harro Seelaar, John C van Swieten, Matthis Synofzik, Raquel Sanchez-Valle, Fermin Moreno, Elizabeth Finger, Mario Masellis, Carmela Tartaglia, Rik Vandenberghe, Robert Laforce, Daniela Galimberti, Barbara Borroni, Chris R Butler, Alexander Gerhard, Simon Ducharme, Jonathan D Rohrer, Anna Månberg, Caroline Graff, Peter Nilsson, Rose Bruffaerts, et al

Cognitive and behavioral manifestations in ALS : beyond motor system involvement

Source
Diagnostics - ISSN 2075-4418-11:4 (2021) p.
Author(s)
Citation link

Shared heritability of human face and brain shape

Source
Nature genetics - ISSN 1061-4036-53:6 (2021) p. 830-839
Author(s)
    Sahin Naqvi, Yoeri Sleyp, Hanne Hoskens, Karlijne Indencleef, Jeffrey P. Spence, Rose Bruffaerts, Ahmed Radwan, Ryan J. Eller, Stephen Richmond, Mark D. Shriver, John R. Shaffer, Seth M. Weinberg, Susan Walsh, James Thompson, Jonathan K. Pritchard, Stefan Sunaert, Hilde Peeters, Joanna Wysocka, Peter Claes
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A 3D deep learning model to predict the diagnosis of dementia with Lewy bodies, Alzheimer's disease, and mild cognitive impairment using brain 18F-FDG PET

Source
European journal of nuclear medicine and molecular imaging - ISSN 1619-7070- (2021) p.
Author(s)
    Kobra Etminani, Amira Soliman, Anette Davidsson, Jose R. Chang, Begona Martinez-Sanchis, Stefan Byttner, Valle Camacho, Matteo Bauckneht, Roxana Stegeran, Marcus Ressner, Marc Agudelo-Cifuentes, Andrea Chincarini, Matthias Brendel, Axel Rominger, Rose Bruffaerts, Rik Vandenberghe, Milica G. Kramberger, Maja Trost, Nicolas Nicastro, Giovanni B. Frisoni, Afina W. Lemstra, Bart N.M. van Berckel, Andrea Pilotto, Alessandro Padovani, Silvia Morbelli, Dag Aarsland, Flavio Nobili, Valentina Garibotto, Miguel Ochoa-Figueroa
Citation link

Neurochemistry and Behaviour

European Academy of Neurology/European Alzheimer's Disease Consortium position statement on diagnostic disclosure, biomarker counseling, and management of patients with mild cognitive impairment

Source
European journal of neurology - ISSN 1351-5101-28:7 (2021) p. 2147-2155
Author(s)
    Kristian Steen Frederiksen, T. Rune Nielsen, Bengt Winblad, Reinhold Schmidt, Milica G. Kramberger, Roy W. Jones, Jakub Hort, Timo Grimmer, Jean Georges, Lutz Frolich, Sebastiaan Engelborghs, Bruno Dubois, Gunhild Waldemar

Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease

Source
Acta neuropathologica communications - ISSN 2051-5960-9:1 (2021) p.
Author(s)

Distinct amyloid-β and tau-associated microglia profiles in Alzheimer’s disease

Source
Acta neuropathologica - ISSN 0001-6322-141 (2021) p. 681-696
Author(s)
    Emma Gerrits, Nieske Brouwer, Susanne M. Kooistra, Maya E. Woodbury, Yannick Vermeiren, Mirjam Lambourne, Jan Mulder, Markus Kummer, Thomas Möller, Knut Biber, Wilfred F.A. den Dunnen, Peter Paul De Deyn, Bart J.L. Eggen, Erik W.G.M. Boddeke

Neuronal Circuit Research

The resting membrane potential of hSC-CM in a syncytium is more hyperpolarised than that of isolated cells

Source
Channels - ISSN 1933-6950-15:1 (2021) p. 239-252
Author(s)

A human importin-β-related disorder : syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8

Source
The American journal of human genetics - ISSN 0002-9297-108:6 (2021) p. 1115-1125
Author(s)