A new prion disease: relationship with central and peripheral amyloidoses

Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations

(2014) R. Guerreiro et al.   HUMAN MOLECULAR GENETICS

Late onset hereditary sensory and autonomic neuropathy with cognitive impairment associated with Y163X prion mutation

(2014) Andreas C. Themistocleous et al.   JOURNAL OF NEUROLOGY

Peripheral alpha-synuclein and Parkinson's disease

(2014) C. Warren Olanow et al.   MOVEMENT DISORDERS

Accumulation of α-synuclein in the bowel of patients in the pre-clinical phase of Parkinson’s disease

(2013) David Hilton et al.   ACTA NEUROPATHOLOGICA

A novel familial prion disease causing pan-autonomic-sensory neuropathy and cognitive impairment

(2013) K. Matsuzono et al.   EUROPEAN JOURNAL OF NEUROLOGY

Submandibular Gland Biopsy for the Diagnosis of Parkinson Disease

(2013) Thomas G. Beach et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Self-propagation of pathogenic protein aggregates in neurodegenerative diseases

(2013) Mathias Jucker et al.   NATURE

Validation of next-generation sequencing technologies in genetic diagnosis of dementia

(2013) John Beck et al.   NEUROBIOLOGY OF AGING

A Novel Prion Disease Associated with Diarrhea and Autonomic Neuropathy

(2013) Simon Mead et al.   NEW ENGLAND JOURNAL OF MEDICINE

Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey

(2013) O. N. Gill et al.   BMJ-British Medical Journal

Amyloid neuropathies

(2012) David Adams et al.   CURRENT OPINION IN NEUROLOGY

Hereditary Systemic Amyloidosis Due to Asp76Asn Variant β2-Microglobulin

(2012) Sophie Valleix et al.   NEW ENGLAND JOURNAL OF MEDICINE

Plasmacytoid Dendritic Cells Sequester High Prion Titres at Early Stages of Prion Infection

(2012) Rocio Castro-Seoane et al.   PLoS Pathogens

Familial prion disease with alzheimer disease-like tau pathology and clinical phenotype

(2011) Suman Jayadev et al.   ANNALS OF NEUROLOGY

Effects of the Known Pathogenic Mutations on the Aggregation Pathway of the Amyloidogenic Peptide of Apolipoprotein A-I

(2011) Sara Raimondi et al.   JOURNAL OF MOLECULAR BIOLOGY

Variable presentations of TTR-related familial amyloid polyneuropathy in seventeen patients

(2011) Manuel Cappellari et al.   JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM

Familial amyloid polyneuropathy

(2011) Violaine Planté-Bordeneuve et al.   LANCET NEUROLOGY

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

(2011) Christopher J Klein et al.   NATURE GENETICS

Gastrointestinal dysfunction contributes to weight loss in Huntington's disease mice

(2011) Jorien M.M. van der Burg et al.   NEUROBIOLOGY OF DISEASE

Variant CJD infection in the spleen of a neurologically asymptomatic UK adult patient with haemophilia

(2010) A. PEDEN et al.   HAEMOPHILIA

Prion Strain Mutation and Selection

(2010) J. Collinge   SCIENCE

Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP

(2009) Casper Jansen et al.   ACTA NEUROPATHOLOGICA

Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies

(2009) Tamas Revesz et al.   ACTA NEUROPATHOLOGICA

Huntington's disease: The current state of research with peripheral tissues

(2009) Jenny Sassone et al.   EXPERIMENTAL NEUROLOGY

Beyond the brain: widespread pathology in Huntington's disease

(2009) Jorien MM van der Burg et al.   LANCET NEUROLOGY

Mortuary rites of the South Fore and kuru

(2008) J. T. Whitfield et al.   PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES