Lucila Autilio-Gambetti

Affiliations: 
Case Western Reserve University, Cleveland Heights, OH, United States 
Area:
Alzheimer disease
Google:
"Lucila Autilio-Gambetti"
Cross-listing: Neurotree - Neuropathology Tree

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Publications

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Parchi P, Petersen RB, Chen SG, et al. (1998) Molecular pathology of fatal familial insomnia. Brain Pathology (Zurich, Switzerland). 8: 539-48
Chen SG, Parchi P, Brown P, et al. (1997) Allelic origin of the abnormal prion protein isoform in familial prion diseases. Nature Medicine. 3: 1009-15
Petersen RB, Tabaton M, Chen SG, et al. (1995) Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17. Neurology. 45: 1062-7
Chen SG, Teplow DB, Parchi P, et al. (1995) Truncated forms of the human prion protein in normal brain and in prion diseases. The Journal of Biological Chemistry. 270: 19173-80
Parchi P, Castellani R, Cortelli P, et al. (1995) Regional distribution of protease-resistant prion protein in fatal familial insomnia. Annals of Neurology. 38: 21-9
Tabaton M, Nunzi MG, Xue R, et al. (1994) Soluble amyloid beta-protein is a marker of Alzheimer amyloid in brain but not in cerebrospinal fluid. Biochemical and Biophysical Research Communications. 200: 1598-603
Petersen RB, Goldfarb LG, Tabaton M, et al. (1994) A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene). Molecular Neurobiology. 8: 99-103
Monari L, Chen SG, Brown P, et al. (1994) Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism. Proceedings of the National Academy of Sciences of the United States of America. 91: 2839-42
Bacci B, Cochran E, Nunzi MG, et al. (1994) Amyloid beta precursor protein and ubiquitin epitopes in human and experimental dystrophic axons. Ultrastructural localization. The American Journal of Pathology. 144: 702-10
Gambetti P, Petersen R, Monari L, et al. (1993) Fatal familial insomnia and the widening spectrum of prion diseases. British Medical Bulletin. 49: 980-94
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