Literature DB >> 1985297

Early-onset Alzheimer's disease in 2 large Belgian families.

J J Martin1, J Gheuens, M Bruyland, P Cras, A Vandenberghe, C L Masters, K Beyreuther, R Dom, C Ceuterick, U Lübke.   

Abstract

Familial Alzheimer's disease (FAD) is a dominantly inherited condition that may present with an early onset, and myoclonus occurs frequently in the course of the disease. We report clinical and neuropathologic data on 2 large Belgian families with FAD in which we obtained 17 autopsies of the CNS. In family A, each of 11 autopsies had the typical neuropathologic features of Alzheimer's disease (AD), and there were a few cerebellar plaques in the molecular layer. In family B, in addition to the typical characteristics of AD in 6 autopsies, there were numerous amyloid plaques in the cortical cerebellar layers. In both families, we immunostained the amyloid deposits for the A4 protein, and they were negative for prion-associated protein immunoreactivity.

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Year:  1991        PMID: 1985297     DOI: 10.1212/wnl.41.1.62

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  11 in total

1.  Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease.

Authors:  D M Mann; S M Pickering-Brown; A Takeuchi; T Iwatsubo
Journal:  Am J Pathol       Date:  2001-06       Impact factor: 4.307

2.  Segregation analysis reveals evidence of a major gene for Alzheimer disease.

Authors:  L A Farrer; R H Myers; L Connor; L A Cupples; J H Growdon
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

3.  Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutation.

Authors:  M Anheim; D Hannequin; C Boulay; C Martin; D Campion; C Tranchant
Journal:  J Neurol Neurosurg Psychiatry       Date:  2007-12       Impact factor: 10.154

4.  Familial cases presenting very early onset autosomal dominant Alzheimer's disease with I143T in presenilin-1 gene: implication for genotype-phenotype correlation.

Authors:  Noritoshi Arai; Atsushi Kishino; Yuji Takahashi; Daiji Morita; Koichiro Nakamura; Takahiro Yokoyama; Tomoji Watanabe; Masayoshi Ida; Jun Goto; Shoji Tsuji
Journal:  Neurogenetics       Date:  2007-10-30       Impact factor: 2.660

5.  The PSEN1 I143T mutation in a Swedish family with Alzheimer's disease: clinical report and quantification of Aβ in different brain regions.

Authors:  Lina Keller; Hedvig Welander; Huei-Hsin Chiang; Lars O Tjernberg; Inger Nennesmo; Asa K Wallin; Caroline Graff
Journal:  Eur J Hum Genet       Date:  2010-07-14       Impact factor: 4.246

Review 6.  Correlating familial Alzheimer's disease gene mutations with clinical phenotype.

Authors:  Natalie S Ryan; Martin N Rossor
Journal:  Biomark Med       Date:  2010-02       Impact factor: 2.851

7.  Paired helical filaments in astrocytes: electron microscopy and immunohistochemistry in a case of atypical Alzheimer's disease.

Authors:  I Nakano; T Iwatsubo; N Otsuka; M Kamei; K Matsumura; T Mannen
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

8.  Presenilin-1 regulates the expression of p62 to govern p62-dependent tau degradation.

Authors:  Ying-Tsen Tung; Bo-Jeng Wang; Wen-Ming Hsu; Ming-Kuan Hu; Guor Mour Her; Wei-Pang Huang; Yung-Feng Liao
Journal:  Mol Neurobiol       Date:  2013-06-23       Impact factor: 5.590

Review 9.  Genetic dissection of Alzheimer disease, a heterogeneous disorder.

Authors:  G D Schellenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1995-09-12       Impact factor: 11.205

Review 10.  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

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