Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Frontotemporal Lobar Degeneration and CHMP2B[original query] |
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| Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland. BMC neurology 2008 8 48. Kaivorinne Anna-Lotta, Krüger Johanna, Kuivaniemi Katja, Tuominen Hannu, Moilanen Virpi, Majamaa Kari, Remes Anne |
| CHMP2B mutations are rare in French families with frontotemporal lobar degeneration. Journal of neurology 2010 Dec 257 (12): 2032-6. Ghanim Mustapha, Guillot-Noel Léna, Pasquier Florence, Jornea Ludmila, Deramecourt Vincent, Dubois Bruno, Le Ber Isabelle, Brice Alexis, |
| Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patients. European journal of neurology : the official journal of the European Federation of Neurological Societies 2010 Nov 17 (11): 1393-5. Kaivorinne A-L, Krüger J, Udd B, Majamaa K, Remes A |
| Mutation Analysis of the Genes Linked to Early Onset Alzheimer's Disease and Frontotemporal Lobar Degeneration. Journal of Alzheimer's disease : JAD 2019 May . Luukkainen Laura, Helisalmi Seppo, Kytövuori Laura, Ahmasalo Riitta, Solje Eino, Haapasalo Annakaisa, Hiltunen Mikko, Remes Anne M, Krüger Johan |
| The association between repeat number in C9orf72 and phenotypic variability in Turkish patients with frontotemporal lobar degeneration. Neurobiology of aging 2019 1 76 216.e1-216.e7. Erzurumluoglu Ebru, Cilingir Oguz, Ozbabalik Adapinar Belgin Demet, Bilgic Basar, Kocagil Sinem, Ozen Hulya, Durak Aras Beyhan, Yenilmez Cinar, Artan Sevilh |
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- Page last updated:Dec 01, 2023
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