Jean Jacques Hauw

Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Disease Phenotype Determined by a DNA Polymorphism

Lev G. Goldfarb, Robert B. Petersen, Massimo Tabaton et al. · Science · 1992 · 716 citations

Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann–Sträussler–Scheinker disease

Piero Parchi, Shu G. Chen, Paul Brown et al. · Proceedings of the National Academy of Sciences · 1998 · 213 citations

A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition

Anne Couturier‐Tarrade, Coralie Fassier, Sabrina Courageot et al. · Human Molecular Genetics · 2006 · 196 citations · Full text

Microtubule Composition, Cytoskeleton, Mechanotransduction +19

Interlaboratory Comparison of Assessments of Alzheimer Disease-Related Lesions: A Study of the BrainNet Europe Consortium

Irina Alafuzoff, Maria Pikkarainen, Safa Al‐Sarraj et al. · Journal of Neuropathology & Experimental Neurology · 2006 · 115 citations

The extent of neurofibrillary pathology in perforant pathway neurons is the key determinant of dementia in the very old

Francisco García‐Sierra, Jean Jacques Hauw, Charles Duyckaerts et al. · Acta Neuropathologica · 2000 · 68 citations

Alzheimer's Disease, Dementia, Neurofibrillary Pathology +12