Literature DB >> 12752408

Early-onset Alzheimer's disease with presenilin-1 M139V mutation: clinical, neuropsychological and neuropathological study.

A J Larner1, D G du Plessis.   

Abstract

The clinical, neuropsychological and neuropathological features of a patient with early-onset Alzheimer's disease as a result of the M139V presenilin-1 (PSEN-1) mutation are presented, and compared with previous reports of patients with the same mutation. Similarities, such as the age at onset and the relative preservation of naming skills, and differences, such as the significant basal ganglia, thalamic and cerebellar pathology, are noted. This clinical and pathological heterogeneity in patients with the same PSEN-1 mutation suggests phenotype modulation by genetic and/or epigenetic factors.

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Year:  2003        PMID: 12752408     DOI: 10.1046/j.1468-1331.2003.00597.x

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  5 in total

1.  Presenilin 1 gene mutation (M139I) in a patient with an early-onset Alzheimer's disease: clinical characteristics and genetic identification.

Authors:  Hee-Jin Kim; Hyun Young Kim; Chang-Seok Ki; Seung Hyun Kim
Journal:  Neurol Sci       Date:  2010-03-06       Impact factor: 3.307

2.  Atypical presentation of a novel Presenilin 1 R377W mutation: sporadic, late-onset Alzheimer disease with epilepsy and frontotemporal atrophy.

Authors:  Barbara Borroni; Andrea Pilotto; Cristian Bonvicini; Silvana Archetti; Antonella Alberici; Andrea Lupi; Massimo Gennarelli; Alessandro Padovani
Journal:  Neurol Sci       Date:  2011-08-06       Impact factor: 3.307

3.  Familial Alzheimer's disease mutations in presenilins: effects on endoplasmic reticulum calcium homeostasis and correlation with clinical phenotypes.

Authors:  Omar Nelson; Charlene Supnet; Huarui Liu; Ilya Bezprozvanny
Journal:  J Alzheimers Dis       Date:  2010       Impact factor: 4.472

4.  Corticobasal Syndrome in a Family with Early-Onset Alzheimer's Disease Linked to a Presenilin-1 Gene Mutation.

Authors:  Eloisa Navarro; Clara De Andrés; Carmen Guerrero; Santiago Giménez-Roldán
Journal:  Mov Disord Clin Pract       Date:  2015-07-25

Review 5.  Clinical phenotypic heterogeneity of Alzheimer's disease associated with mutations of the presenilin-1 gene.

Authors:  A J Larner; M Doran
Journal:  J Neurol       Date:  2005-11-04       Impact factor: 6.682

  5 in total

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