Search Results - "DUYCKAERTS, C"

Neurodegenerative lesions: Seeding and spreading by Duyckaerts, C.

“…Accumulation of specific proteins has replaced loss of specific populations of neurons in the definition of most neurodegenerative diseases. In some cases, the…”
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Cognitive deficit, and neuropathological correlates, in the oldest-old by Verny, M., Duyckaerts, C.

“…Several disorders are usually involved in the cognitive deficit of the oldest old. Alzheimer disease is the commonest. It is usually characterized by…”
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STochastic Optical Reconstruction Microscopy (STORM) reveals the nanoscale organization of pathological aggregates in human brain by Codron, P., Letournel, F., Marty, S., Renaud, L., Bodin, A., Duchesne, M., Verny, C., Lenaers, G., Duyckaerts, C., Julien, J.‐P., Cassereau, J., Chevrollier, A.

“…Aims Histological analysis of brain tissue samples provides valuable information about the pathological processes leading to common neurodegenerative…”
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Office of Rare Diseases Neuropathologic Criteria for Corticobasal Degeneration by DICKSON, D W, BERGERON, C, CHIN, S S, DUYCKAERTS, C, HOROUPIAN, D, IKEDA, K, JELLINGER, K, LANTOS, P L, LIPPA, C F, MIRRA, S S, TABATON, M, VONSATTEL, J P, WAKABAYASHI, K, LITVAN, I

“…A working group supported by the Office of Rare Diseases of the National Institutes of Health formulated neuropathologic criteria for corticobasal degeneration…”
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Valosin-containing protein gene mutations : Clinical and neuropathologic features by GUYANT-MARECHAL, L, LAQUERRIERE, A, DUYCKAERTS, C, DUMANCHIN, C, BOU, J, DUGNY, F, LE BER, I, FREBOURG, T, HANNEQUIN, D, CAMPION, D

“…Hereditary inclusion body myopathy (IBMPFD) with Paget disease of bone (PDB) and frontotemporal dementia (FTD) is a rare multisystem disorder with autosomal…”
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JC-virus-related progressive multifocal leukoencephalopathy in a myasthenic patient treated by rituximab by Eymard, B, Rigolet, A, Nguyen, L, Rozenberg, F, Afanasief, V, Duyckaerts, C, Benveniste, O

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Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease by LE BER, I, CAMUZAT, A, HEATH, S, CAMU, W, MARTINAUD, O, LACOMBLEZ, L, VERCELLETTO, M, SALACHAS, F, SELLAL, F, DIDIC, M, THOMAS-ANTERION, C, PUEL, M, BERGER, E, MICHEL, B.-F, BESSE, C, DUYCKAERTS, C, MEININGER, V, CAMPION, D, DUBOIS, B, BRICE, A, HANNEQUIN, D, LAQUERRIERE, A, GOLFIER, V, SEILHEAN, D, VIENNET, G, COURATIER, P, VERPILLAT, P

“…Frontotemporal dementia associated with motor neuron disease (FTD-MND) is a rare neurodegenerative disorder that may be inherited by autosomal dominant trait…”
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Alzheimer pathology disorganizes cortico-cortical circuitry: direct evidence from a transgenic animal model by Delatour, B, Blanchard, V, Pradier, L, Duyckaerts, C

“…It has been proposed that Alzheimer disease (AD) is associated with a “disconnection syndrome” due to the gradual loss of morphological and functional…”
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Neuroserpin mutation causes electrical status epilepticus of slow-wave sleep by Coutelier, M, Andries, S, Ghariani, S, Dan, B, Duyckaerts, C, van Rijckevorsel, K, Raftopoulos, C, Deconinck, N, Sonderegger, P, Scaravilli, F, Vikkula, M, Godfraind, C

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Spreading of protein misfolding: A new paradigm in neurology by Hauw, J-J, Haïk, S, Duyckaerts, C

“…Protein misfolding and spreading ("transconformation") are being better understood. Described in Prions diseases, this new paradigm in the field of…”
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Consensus Recommendations for the Postmortem Diagnosis of Alzheimer’s Disease by KHACHATURIAN, Zaven, PHELPS, Creighton, TROJANOWSKI, John Q

“…This report summarizes the consensus recommendations of a panel of neuropathologists from the United States and Europe to improve the postmortem diagnostic…”
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Frontotemporal lobar degeneration: Diversity of FTLD lesions by Seilhean, D., Bielle, F., Plu, I., Duyckaerts, C.

“…Frontotemporal lobar degeneration (FTLD) is a heterogeneous group including both sporadic and familial diseases, characterized by a macroscopic alteration. It…”
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Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease by CAIRNS, N. J, GROSSMAN, M, CRUZ-SANCHEZ, F. F, BIGIO, E. H, MACKENZIE, I. R. A, GEARING, M, JUNCOS, J. L, GLASS, J. D, YOKOO, H, NAKAZATO, Y, MOSAHEB, S, THORPE, J. R, ARNOLD, S. E, URYU, K, LEE, V. M.-Y, TROJANOWSKI, J. Q, BURN, D. J, JAROS, E, PERRY, R. H, DUYCKAERTS, C, STANKOFF, B, PILLON, B, SKULLERUD, K

“…Recently described neuronal intermediate filament inclusion disease (NIFID) shows considerable clinical heterogeneity. To assess the spectrum of the clinical…”
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Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis by Namekawa, M., Muriel, M.-P., Janer, A., Latouche, M., Dauphin, A., Debeir, T., Martin, E., Duyckaerts, C., Prigent, A., Depienne, C., Sittler, A., Brice, A., Ruberg, M.

“…Mutations in SPG3A causing autosomal dominant pure spastic paraplegia led to identification of atlastin, a new dynamin-like large GTPase. Atlastin is localized…”
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Nosology of dementias: the neuropathologist's point of view by Duyckaerts, C

“…The diagnosis of degenerative dementias heavily relies on the identification of neuronal or glial inclusions. Tauopathy is probably the largest group including…”
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Modifications of the endosomal compartment in peripheral blood mononuclear cells and fibroblasts from Alzheimer’s disease patients by Corlier, F, Rivals, I, Lagarde, J, Hamelin, L, Corne, H, Dauphinot, L, Ando, K, Cossec, J-C, Fontaine, G, Dorothée, G, Malaplate-Armand, C, Olivier, J-L, Dubois, B, Bottlaender, M, Duyckaerts, C, Sarazin, M, Potier, M-C

“…Identification of blood-based biomarkers of Alzheimer’s disease (AD) remains a challenge. Neuropathological studies have identified enlarged endosomes in…”
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Abnormal TDP-43 and FUS proteins in muscles of sporadic IBM: similarities in a TARDBP-linked ALS patient by Hernandez Lain, Aurelio, Millecamps, Stéphanie, Dubourg, Odile, Salachas, François, Bruneteau, Gaëlle, Lacomblez, Lucette, LeGuern, Eric, Seilhean, Danielle, Duyckaerts, Charles, Meininger, Vincent, Mallet, Jacques, Pradat, Pierre-François

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Clinical and neuropathologic study of a french family with a mutation in the neuroserpin gene by GOURFINKEL-AN, I, DUYCKAERTS, C, CAMUZAT, A, MEYRIGNAC, C, SONDEREGGER, P, BAULAC, M, BRICE, A

“…Familial encephalopathy with neuroserpin inclusion bodies is a recently described neurodegenerative disease that is responsible for progressive myoclonic…”
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Prevalence of nephroangiosclerosis in patients with fatal stroke by ABBOUD, H, LABREUCHE, J, DUYCKAERTS, C, HAUW, J.-J, AMARENCO, P

“…Glomerular filtration rate and decline in renal function can be improved by global cardiovascular prevention. However, the prevalence of nephroangiosclerosis…”
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P5.26 Myopathy associated with HIV, a review of 50 muscle biopsies by Allenbach, Y, Dubourg, O, Maisonobe, T, Herson, S, Duyckaerts, C, Benveniste, O

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