J.-J Martin
Affiliations: | Universiteit Antwerpen (Belgium) |
Area:
Mental Health, Cognitive Psychology, Psychometrics PsychologyGoogle:
"J.-J Martin"Mean distance: 53433
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Publications
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| Smolders S, Philtjens S, Crosiers D, et al. (2021) Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease. Acta Neuropathologica Communications. 9: 25 |
| Eidhof I, Baets J, Kamsteeg EJ, et al. (2018) GDAP2 mutations implicate susceptibility to cellular stress in a new form of cerebellar ataxia. Brain : a Journal of Neurology |
| Sieben A, Van Mossevelde S, Wauters E, et al. (2018) Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family. Alzheimer's Research & Therapy. 10: 7 |
| Van den Bossche T, Sleegers K, Cuyvers E, et al. (2016) Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation. Neurology |
| 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 |
| van der Zee J, Van Langenhove T, Kovacs GG, et al. (2014) Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration. Acta Neuropathologica. 128: 397-410 |
| 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 |
| Van Langenhove T, van der Zee J, Gijselinck I, et al. (2013) Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort. Jama Neurology. 70: 365-73 |
| Scalais E, Francois B, Schlesser P, et al. (2012) Polymerase gamma deficiency (POLG): clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh's encephalopathy. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 16: 542-8 |
| van der Zee J, Pirici D, Van Langenhove T, et al. (2009) Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His. Neurology. 73: 626-32 |