No association of chromatin-modifying protein 2B with sporadic frontotemporal dementia-Reference-Cited by-同舟云学术

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No association of chromatin-modifying protein 2B with sporadic frontotemporal dementia

Published:2007-11 Issue:11 Volume:28 Page:1789-1790
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Schumacher Axel,Friedrich Patricia,Diehl-Schmid Janine,Ibach Bernd,Eisele Tamara,Laws Simon M.,Förstl Hans,Kurz Alexander,Riemenschneider Matthias

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference13 articles.

1. Haploview: analysis and visualization of LD and haplotype maps;Barrett;Bioinformatics,2005

2. CHMP2B mutations are not a common cause of frontotemporal lobar degeneration;Cannon;Neurosci Lett,2006

3. ‘Mini Mental State’. A practical method for grading the cognitive state of patients for the clinician;Folstein;J Psychiat Res,1975

4. A common LRRK2 mutation in idiopathic Parkinson's disease;Gilks;Lancet,2005

5. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17;Hutton;Nature,1998

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1. Frontotemporal dementia;Neurogenetics, Part II;2018

2. Frontotemporal dementia: latest evidence and clinical implications;Therapeutic Advances in Psychopharmacology;2017-11-10

3. FTD and ALS: A Tale of Two Diseases;Current Alzheimer Research;2011-05-01

4. Novel Missense Mutation in Charged Multivesicular Body Protein 2B in a Patient With Frontotemporal Dementia;Alzheimer Disease & Associated Disorders;2010-10

5. Mutations inCHMP2Bare not a cause of frontotemporal lobar degeneration in Finnish patients;European Journal of Neurology;2010-04-20

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