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Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies.
Forrest, Shelley L; Kril, Jillian J; Stevens, Claire H; Kwok, John B; Hallupp, Marianne; Kim, Woojin S; Huang, Yue; McGinley, Ciara V; Werka, Hellen; Kiernan, Matthew C; Götz, Jürgen; Spillantini, Maria Grazia; Hodges, John R; Ittner, Lars M; Halliday, Glenda M.
Affiliation
  • Forrest SL; Charles Perkins Centre and Discipline of Pathology, Sydney Medical School, University of Sydney, Australia.
  • Kril JJ; Charles Perkins Centre and Discipline of Pathology, Sydney Medical School, University of Sydney, Australia.
  • Stevens CH; Dementia Research Unit, School of Medical Sciences, University of New South Wales, Australia.
  • Kwok JB; Brain and Mind Centre and Central Clinical School, Sydney Medical School, University of Sydney, Australia.
  • Hallupp M; Neuroscience Research Australia, Sydney, Australia.
  • Kim WS; School of Medical Sciences, University of New South Wales, Australia.
  • Huang Y; Brain and Mind Centre and Central Clinical School, Sydney Medical School, University of Sydney, Australia.
  • McGinley CV; Brain and Mind Centre and Central Clinical School, Sydney Medical School, University of Sydney, Australia.
  • Werka H; Neuroscience Research Australia, Sydney, Australia.
  • Kiernan MC; School of Medical Sciences, University of New South Wales, Australia.
  • Götz J; School of Medical Sciences, University of New South Wales, Australia.
  • Spillantini MG; Charles Perkins Centre and Discipline of Pathology, Sydney Medical School, University of Sydney, Australia.
  • Hodges JR; Charles Perkins Centre and Discipline of Pathology, Sydney Medical School, University of Sydney, Australia.
  • Ittner LM; Brain and Mind Centre and Central Clinical School, Sydney Medical School, University of Sydney, Australia.
  • Halliday GM; Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, The University of Queensland, Australia.
Brain ; 141(2): 521-534, 2018 02 01.
Article de En | MEDLINE | ID: mdl-29253099
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Protéines tau / Tauopathies / Démence frontotemporale / Mutation Type d'étude: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Aged / Female / Humans / Male / Middle aged Langue: En Journal: Brain Année: 2018 Type de document: Article Pays d'affiliation: Australie
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Protéines tau / Tauopathies / Démence frontotemporale / Mutation Type d'étude: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Aged / Female / Humans / Male / Middle aged Langue: En Journal: Brain Année: 2018 Type de document: Article Pays d'affiliation: Australie