R B Alvarez

发表

Fourteen Newly Recognized Proteins at the Human Neuromuscular Junctions‐and Their Nonjunctional Accumulation in Inclusion‐Body Myositisa a

W. Engel, V. Askanas, V Askanas, 1998, Annals of the New York Academy of Sciences.

beta-Amyloid protein immunoreactivity in muscle of patients with inclusion-body myositis.

W. Engel, G. Glenner, V. Askanas, 1992, Lancet.

Immunocytochemical localization of ubiquitin in inclusion body myositis allows its light‐microscopic distinction from polymyositis

W. Engel, V. Askanas, V Askanas, 1992, Neurology.

Strong immunoreactivity of beta-amyloid precursor protein, including the beta-amyloid protein sequence, at human neuromuscular junctions.

W. Engel, V. Askanas, V Askanas, 1992, Neuroscience letters.

Prion protein is abnormally accumulated in inclusion‐body myositis

W. Engel, F. Tomé, V. Askanas, 1993, Neuroreport.

Nitric oxide-induced oxidative stress in autosomal recessive and dominant inclusion-body myopathies.

W. Engel, S. Heller, V. Askanas, 1998, Brain : a journal of neurology.

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.

W. Engel, T. Wisniewski, V. Askanas, 1998, The American journal of pathology.

Enhanced detection of Congo‐red‐positive amyloid deposits in muscle fibers of inclusion body myositis and brain of Alzheimer's disease using fluorescence technique

W. Engel, V. Askanas, V Askanas, 1993, Neurology.

Light and electron microscopic localization of beta-amyloid protein in muscle biopsies of patients with inclusion-body myositis.

W. Engel, V. Askanas, V Askanas, 1992, The American journal of pathology.

beta-Amyloid precursor epitopes in muscle fibers of inclusion body myositis.

W. Engel, V. Askanas, V Askanas, 1993, Annals of neurology.

Difference in Expression of Phosphorylated Tau Epitopes between Sporadic Inclusion‐body Myositis and Hereditary Inclusion‐body Myopathies

W. Engel, M. Mirabella, V. Askanas, 1996, Journal of neuropathology and experimental neurology.

βAPP gene transfer into cultured human muscle induces inclusion‐body myositis aspects

W. Engel, V. Askanas, V Askanas, 1997 .

Increase of nitric oxide synthases and nitrotyrosine in inclusion‐body myositis

W. Engel, V. Askanas, V Askanas, 1996, Neuroreport.

Paired helical filaments of inclusion-body myositis muscle contain RNA and survival motor neuron protein.

V Askanas, W K Engel, R B Alvarez, 2000, The American journal of pathology.

Twisted tubulofilaments of inclusion body myositis muscle resemble paired helical filaments of Alzheimer brain and contain hyperphosphorylated tau.

D. Selkoe, W. Engel, V. Askanas, 1994, The American journal of pathology.

beta-Amyloid precursor protein mRNA is increased in inclusion-body myositis muscle.

W. Engel, V. Askanas, V Askanas, 1993, Neuroreport.