Area of research
Molecular Biology · Neurology
Research interest
Research interests include Prion Diseases and Protein Misfolding, Neurological diseases and metabolism, Trace Elements in Health, and Glioma Diagnosis and Treatment.
High-Depth PRNP Sequencing in Brains With Sporadic Creutzfeldt-Jakob Disease.
Serpin Signatures in Prion and Alzheimer's Diseases.
Wide distribution of prion infectivity in the peripheral tissues of vCJD and sCJD patients.
Association of baseline hematoma and edema volumes with one-year outcome and long-term survival after spontaneous intracerebral hemorrhage: A community-based inception cohort study.
Prion strains associated with iatrogenic CJD in French and UK human growth hormone recipients.
Prevalence in Britain of abnormal prion protein in human appendices before and after exposure to the cattle BSE epizootic.
Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures.
Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates.
Spinal subependymoma surgery: do no harm. Little may be more!
Convalescent plasma for administration of passive antibodies against viral agents.
Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.
Frequency and signature of somatic variants in 1461 human brain exomes.
Variably protease-sensitive prionopathy mimicking frontotemporal dementia.
Frequency and signature of somatic variants in 1461 human brain exomes
A European randomised controlled trial of the addition of etoposide to standard vincristine and carboplatin induction as part of an 18-month treatment programme for childhood (≤16 years) low grade glioma – A final report
Prion seeding activity and infectivity in skin samples from patients with sporadic Creutzfeldt-Jakob disease
Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains
Human stem cell–derived astrocytes replicate human prions in a <i>PRNP</i> genotype–dependent manner
Vascular cognitive impairment neuropathology guidelines (VCING): the contribution of cerebrovascular pathology to cognitive impairment
Post-mortem histopathology underlying β-amyloid PET imaging following flutemetamol F 18 injection
Florbetaben PET imaging to detect amyloid beta plaques in Alzheimer's disease: Phase 3 study
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy
BrainNet Europe’s Code of Conduct for brain banking
Current concepts in the prevention of pathogen transmission via blood/plasma-derived products for bleeding disorders
Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium
Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA
Neuropathology of the hippocampus in FTLD‐Tau with Pick bodies: a study of the BrainNet Europe Consortium
The need to unify neuropathological assessments of vascular alterations in the ageing brain