Evidence of CNS β-amyloid deposition in Nasu-Hakola disease due to the TREM2 Q33X mutation-Reference-Cited by-同舟云学术

Evidence of CNS β-amyloid deposition in Nasu-Hakola disease due to the TREM2 Q33X mutation

Published:2017-11-15 Issue:24 Volume:89 Page:2503-2505
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Ghezzi Laura,Carandini Tiziana,Arighi Andrea,Fenoglio Chiara,Arcaro Marina,De Riz Milena,Pietroboni Anna M.,Fumagalli Giorgio G.,Basilico Paola,Calvi Alberto,Scarioni Marta,Colombi Annalisa,Serpente Maria,Marotta Giorgio,Benti Riccardo,Scarpini Elio,Galimberti Daniela

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Reference7 articles.

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2. Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL): a new report of an Italian woman and review of the literature;Bock;J Neurol Sci,2013

3. A case of Nasu-Hakola disease without fractures or consanguinity diagnosed using exome sequencing and treated with sodium valproate;Yamazaki;Clin Psychopharmacol Neurosci,2015

4. Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement

5. TREM2 Variants in Alzheimer's Disease

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