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Characterization of the human analogue of a Scrapie-responsive geneIncreased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathologyCerebellar infarction in the territory of the anterior and inferior cerebellar artery. A clinicopathological study of 20 casesParamyotonia congenita: genotype to phenotype correlations in two families and report of a new mutation in the sodium channel geneQuantitative study of lateral horn cells in 15 cases of multiple system atrophyGanglioside GD1b is the target antigen for a biclonal IgM in a case of sensory-motor axonal polyneuropathy: involvement of N-acetylneuraminic acid in the epitopePeripheral-nerve lipid abnormalities in patients on perhexiline maleateElectron microscopic study of nerve, muscle and skin lesions induced by perhexiline maleate (author's transl)Peripheral neuropathies due to perhexiline maleate (author's transl)Diffuse polymorphous inclusions in a patient treated with perhexiline maleate (author's transl)Neurological disorders and perhexiline maleate therapy. Clinical study of 10 cases. Neuropathological, pharmacocinetic and biochemical studies (author's transl)Analysis of the major lipid classes in human peripheral nerve biopsies. Age group differences and abnormalities of ganglioside level in perhexiline maleate therapyAmiodaron neuropathy: clinical and pathological study of a new drug induced lipidosis (author's transl)Beyond PrP9res) type 1/type 2 dichotomy in Creutzfeldt-Jakob diseaseIs the urea cycle involved in Alzheimer's disease?In vivo detection of thalamic gliosis: a pathoradiologic demonstration in familial fatal insomnia.Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strains.Rapid onset frontal leukodystrophy with decreased diffusion coefficient and neuroaxonal spheroids.Nodes of ranvier and paranodes in chronic acquired neuropathiesTwo populations of neuronal intranuclear inclusions in SCA7 differ in size and promyelocytic leukaemia protein content.Selective loss of cholinergic neurons in the ventral striatum of patients with Alzheimer disease.Mixed dementia: epidemiology, diagnosis, and treatment.Dementia, the fate of brain? Neuropathological point of view.Adaptation of the bovine spongiform encephalopathy agent to primates and comparison with Creutzfeldt-- Jakob disease: implications for human healthBrain targeting through the autonomous nervous system: lessons from prion diseases.Fragmentation of the Golgi apparatus of motor neurons in amyotrophic lateral sclerosisDifferent patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease.Golgi apparatus, GERL, and lysosomes of neurons in rat dorsal root ganglia, studied by thick section and thin section cytochemistry.[Quantitative and electron microscope study of the nerve in seven cases of sporadic idiopathic sensory neuropathy (author's transl)].Pathways of migration of transplanted Schwann cells in the demyelinated mouse spinal cord.Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USAADAM30 Downregulates APP-Linked Defects Through Cathepsin D Activation in Alzheimer's Disease.Neuropathology of central nervous system arterial syndromes. Part I: the supratentorial circulation.Neuropathology of sleep disorders: a review.
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P50
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neuropatólogo francés
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neuropatólogu francés
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Jean-Jacques Hauw
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Jean-Jacques Hauw
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1941-08-26T00:00:00Z
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