J.-J Martin

Universiteit Antwerpen (Belgium) 
Mental Health, Cognitive Psychology, Psychometrics Psychology
"J.-J Martin"
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Van den Bossche T, Sleegers K, Cuyvers E, et al. (2016) Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation. Neurology
Van Mossevelde S, van der Zee J, Gijselinck I, et al. (2015) Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort. Brain : a Journal of Neurology
Gijselinck I, Van Mossevelde S, van der Zee J, et al. (2015) Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort. Neurology
Janssens J, Philtjens S, Kleinberger G, et al. (2015) Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains. Acta Neuropathologica Communications. 3: 68
Gijselinck I, Van Mossevelde S, van der Zee J, et al. (2015) The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter. Molecular Psychiatry
Semmler AL, Sacconi S, Bach JE, et al. (2014) Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies. Orphanet Journal of Rare Diseases. 9: 121
Kleinberger G, Yamanishi Y, Suárez-Calvet M, et al. (2014) TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis. Science Translational Medicine. 6: 243ra86
Götzl JK, Mori K, Damme M, et al. (2014) Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis. Acta Neuropathologica. 127: 845-60
Gallagher MD, Suh E, Grossman M, et al. (2014) TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions. Acta Neuropathologica. 127: 407-18
Dohrn MF, Röcken C, De Bleecker JL, et al. (2013) Diagnostic hallmarks and pitfalls in late-onset progressive transthyretin-related amyloid-neuropathy. Journal of Neurology. 260: 3093-108
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