Amyloid-β42 is preferentially accumulated in muscle fibers of patients with sporadic inclusion-body myositis

Author:

Vattemi Gaetano,Nogalska Anna,King Engel W.,D’Agostino Carla,Checler Frederic,Askanas Valerie

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Reference36 articles.

1. Askanas V, Engel WK, Alvarez RB (1992) Light-and electron microscopic localization of β-amyloid protein in muscle biopsies of patients with inclusion-body myositis. Am J Pathol 141:31–36

2. Askanas V, Alvarez RB, Engel WK (1993) Beta-amyloid precursor epitopes in muscle fibers of inclusion body myositis. Ann Neurol 34:551–560. doi: 10.1002/ana.410340408

3. Askanas V, Engel WK, Alvarez RB (1993) Enhanced detection of Congo-red positive amyloid deposits in muscle fibers of inclusion-body myositis and brain of Alzheimer’s disease using fluorescence technique. Neurology 43:1265–1267

4. Askanas V, Engel WK (1998) Does overexpression of AßPP in aging muscle have a pathogenic role and relevance to Alzheimer’s disease? Am J Pathol 153:1673–1677

5. Askanas V, Engel WK, Yang CC, Alvarez RB, Lee VM, Wisniewski T (1998) Light and electron microscopic immunolocalization of presenilin 1 in abnormal muscle fibers of patients with sporadic inclusion-body myositis and autosomal-recessive inclusion-body myopathy. Am J Pathol 152:889–895

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