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Review: PrP 106‐126 – 25 years after

Neuropathology and applied neurobiology, 2019-08, Vol.45 (5), p.430-440

2019

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The many ways to frontotemporal degeneration and beyond

Neurological sciences, 2007-10, Vol.28 (5), p.241-244

Bugiani, O

2007

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Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain

Neurology, 1999-12, Vol.53 (9), p.2173

1999

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Tauopathy in human and experimental variant Creutzfeldt-Jakob disease

Neurobiology of aging, 2008-12, Vol.29 (12), p.1864-1873

2008

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A beta-related cerebral amyloid angiopathy

Neurological sciences, 2004-03, Vol.25 Suppl 1, p.S1-S2

Bugiani, O

2004

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Neuropathology of the dementias other than Alzheimer's

Neurological sciences, 2006-03, Vol.27 Suppl 1 (S1), p.S44-s46

Bugiani, O

2006

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Effectiveness of anthracycline against experimental prion disease in Syrian hamsters

Science (American Association for the Advancement of Science), 1997-05, Vol.276 (5315), p.1119-1122

1997

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Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation

Neurology, 2010-03, Vol.74 (10), p.798-806

2010

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A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene

Neurology, 2004-09, Vol.63 (5), p.910-912

2004

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Conformational polymorphism of the amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein

The Journal of biological chemistry, 1994-03, Vol.269 (11), p.7859-7862

1994

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A -related cerebral amyloid angiopathy

Neurological sciences, 2004-03, Vol.25, p.s1-s2

Bugiani, O.

2004

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Vascular Variant of Prion Protein Cerebral Amyloidosis with τ -Positive Neurofibrillary Tangles: The Phenotype of the Stop Codon 145 Mutation in PRNP

Proceedings of the National Academy of Sciences - PNAS, 1996-01, Vol.93 (2), p.744-748

1996

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CT and MR Imaging of Neuroaxonal Leukodystrophy Presenting as Early-Onset Frontal Dementia

American Journal of Neuroradiology, 2006-05, Vol.27 (5), p.1037-1039

2006

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Molecular Characteristics of a Protease-Resistant, Amyloidogenic and Neurotoxic Peptide Homologous to Residues 106-126 of the Prion Protein

Biochemical and biophysical research communications, 1993-08, Vol.194 (3), p.1380-1386

1993

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A novel phenotype of sporadic Creutzfeldt–Jakob disease

Journal of neurology, neurosurgery and psychiatry, 2007-12, Vol.78 (12), p.1379-1382

2007

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Chronic high frequency stimulation of the posteromedial hypothalamus in facial pain syndromes and behaviour disorders

Acta neurochirurgica. Supplement, 2007, Vol.97 (Pt 2), p.399

2007

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Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation

Journal of Neural Transmission, 2007-07, Vol.114 (7), p.947-950

2007

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Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria

Neurology, 1999-04, Vol.52 (7), p.1472-1472

1999

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Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene

Neurology, 2003-11, Vol.61 (9), p.1288-1291

2003

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Familial frontotemporal dementia associated with the novel MAPT mutation T427M

Journal of neurology, 2005-12, Vol.252 (12), p.1543-1545

2005

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Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene

Neurology, 2000-08, Vol.55 (3), p.405-410

2000

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Fatal familial insomnia: genetic, neuropathologic, and biochemical study of a patient from a new Italian kindred

Neurology, 1998-03, Vol.50 (3), p.688-692

1998

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Fatal familial insomnia: clinical and pathologic study of five new cases

Neurology, 1992-02, Vol.42 (2), p.312-312

1992

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Review: PrP 106‐126 – 25 years after

The many ways to frontotemporal degeneration and beyond

Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain

Tauopathy in human and experimental variant Creutzfeldt-Jakob disease

A beta-related cerebral amyloid angiopathy

Neuropathology of the dementias other than Alzheimer's

Effectiveness of anthracycline against experimental prion disease in Syrian hamsters

Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation

A family with Alzheimer disease and strokes associated with A713T mutation of the APP gene

Conformational polymorphism of the amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion protein

A -related cerebral amyloid angiopathy

Vascular Variant of Prion Protein Cerebral Amyloidosis with τ -Positive Neurofibrillary Tangles: The Phenotype of the Stop Codon 145 Mutation in PRNP

CT and MR Imaging of Neuroaxonal Leukodystrophy Presenting as Early-Onset Frontal Dementia

Molecular Characteristics of a Protease-Resistant, Amyloidogenic and Neurotoxic Peptide Homologous to Residues 106-126 of the Prion Protein

A novel phenotype of sporadic Creutzfeldt–Jakob disease

Chronic high frequency stimulation of the posteromedial hypothalamus in facial pain syndromes and behaviour disorders

Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation

Staging/typing of Lewy body related α-synuclein pathology: a study of the BrainNet Europe Consortium

Infantile neuroaxonal dystrophy: clinical spectrum and diagnostic criteria

Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene

Familial frontotemporal dementia associated with the novel MAPT mutation T427M

Assessment of β-amyloid deposits in human brain: a study of the BrainNet Europe Consortium

Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene

Fatal familial insomnia: genetic, neuropathologic, and biochemical study of a patient from a new Italian kindred

Fatal familial insomnia: clinical and pathologic study of five new cases

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