Zobrazeno 1 - 10 of 74 pro vyhledávání: '"Béatrice Mougenot"'
1
ANCA-related crescentic glomerulonephritis in systemic sclerosis: revisiting the ?normotensive scleroderma renal crisis?
Autor: Laurent Arnaud, Emmanuelle Plaisier, Antoine Huart, Béatrice Mougenot, J.P. Rougier, K Tiev, Hélène François, A Kettaneh, Pierre Ronco
Publikováno v: Clinical Nephrology. 68:165-170
The scleroderma renal crisis is characterized by acute onset of severe hypertension and by rapidly progressive hyperreninemic renal failure. There is, however, a very limited subset of patients with rapidly progressive renal failure who remain normot
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb93b8908f990a5b828e030162651825
https://doi.org/10.5414/cnp68165
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3
Risk Factors for Early Epithelial to Mesenchymal Transition in Renal Grafts
Autor: P. Sebe, Alexandre Hertig, Denis Glotz, Chantal Jouanneau, Nacera Ouali, Jérôme Verine, Eric Rondeau, Pierre-Yves Ancel, Yi-Chun Xu-Dubois, Béatrice Mougenot
Publikováno v: American Journal of Transplantation. 6:2937-2946
Epithelial-to-mesenchymal transition (EMT) of tubular epithelial cells (TECs) may participate in the pathogenesis of renal fibrosis. We performed a prospective study of EMT markers in protocol biopsies obtained 3 months after engraftment from 56 pati
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44f9d667cdfb8ca1c8afe129731f94ef
https://doi.org/10.1111/j.1600-6143.2006.01559.x
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4
Immunoglobulin light (heavy)-chain deposition disease: from molecular medicine to pathophysiology-driven therapy.: Light-chain deposition disease
Autor: Pierre Aucouturier, Pierre Ronco, Béatrice Mougenot, Emmanuelle Plaisier
Publikováno v: Clinical Journal of the American Society of Nephrology
Clinical Journal of the American Society of Nephrology, American Society of Nephrology, 2006, 1 (6), pp.1342-50. ⟨10.2215/CJN.01730506⟩
Clinical Journal of the American Society of Nephrology, 2006, 1 (6), pp.1342-50. ⟨10.2215/CJN.01730506⟩
8 pages; Light-, light- and heavy-, and heavy-chain deposition diseases belong to a family of diseases that include light-chain (AL)-amyloid, nonamyloid fibrillary and immunotactoid glomerulonephritis, and cryoglobulinemic glomerulonephritis, in whic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0e12116e4984386f6748859e4b68e5e
https://doi.org/10.2215/cjn.01730506
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5
Glomerular Permeability Is Altered by Loss of P0, a Myelin Protein Expressed in Glomerular Epithelial Cells
Autor: Chantal Jouanneau, Rudolf Martini, Dontscho Kerjaschki, Joan J. Archelos, Pierre Ronco, Béatrice Mougenot, Marie Christine Verpont, Emmanuelle Plaisier
Publikováno v: Journal of the American Society of Nephrology. 16:3350-3356
The myelin protein 0 (MPZ or P0) is a transmembrane glycoprotein that represents the most abundant myelin component. Mutations in the P0 gene are associated with one form of autosomal dominant demyelinating peripheral neuropathy, Charcot-Marie-Tooth
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00cff46f6d6846acdf21e37526303646
https://doi.org/10.1681/asn.2005050509
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6
A Cluster of Mutations in the UMOD Gene Causes Familial Juvenile Hyperuricemic Nephropathy with Abnormal Expression of Uromodulin
Autor: Corinne Antignac, Didier Vertommen, Christine Verellen-Dumoulin, Dominique Chauveau, Béatrice Mougenot, Guy Loute, Pierre Cochat, Marie-France Gagnadoux, Christian Jacquot, Mark H. Rider, Jean-Pierre Cosyns, Yves Pirson, Karin Dahan, Olivier Devuyst, M Smaers, Béatrice Viron, Jean-Michel Poux, Mathias Büchler
Publikováno v: Journal of the American Society of Nephrology. 14:2883-2893
Familial juvenile hyperuricemic nephropathy (FJHN [MIM 162000]) is an autosomal-dominant disorder characterized by abnormal tubular handling of urate and late development of chronic interstitial nephritis leading to progressive renal failure. A locus
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4592ac59bee5d55f5818f09032024e2a
https://doi.org/10.1097/01.asn.0000092147.83480.b5
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7
The Spectrum of Systemic Involvement in Adults Presenting with Renal Lesion and Mitochondrial tRNA(Leu) Gene Mutation
Autor: Sophie Lebon, Agnès Rötig, Béatrice Mougenot, Laure-Hélène Noël, Dominique Chauveau, Christine Bellané-Chantelot, Pierre Clavel, Pierre Rustin, Jean-Pierre Grünfeld, Bruno Guéry, Gabriel Choukroun
Publikováno v: ResearcherID
The A3243G mutation of the mitochondrial tRNA(Leu) gene has been recently reported in rare patients with focal and segmental glomerulosclerosis (FSGS). However, the full spectrum of systemic and kidney manifestations in adults presenting with this mu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86fb4bfe2a381fd4332b080425f2c113
https://doi.org/10.1097/01.asn.0000080180.51098.02
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8
Antenatal Membranous Glomerulonephritis with Vascular Injury Induced by Anti-Neutral Endopeptidase Antibodies
Autor: Albert Bensman, Jean-Philippe Haymann, Vincent Guigonis, Pierre Ronco, Georges Deschênes, Hanna Debiec, Béatrice Mougenot
Publikováno v: Scopus-Elsevier
Membranous glomerulonephritis is a major cause of nephrotic syndrome and chronic renal insufficiency. This condition may be associated with a wide spectrum of infections, cancers, autoimmune diseases, and drugs, although primary forms of the disease
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::866f34a8378c42c8be1ca863ff5b0642
https://doi.org/10.1097/01.asn.0000067649.64849.75
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9
Anti-glomerular basement membrane nephritis and bullous pemphigoid caused by distinct anti-α3(IV)NC1 and anti-BP180 antibodies in a patient with Crohn's disease
Autor: Marie-José Wattiaux, Luca Borradori, Béatrice Mougenot, Thomas Hellmark, Béatrice Flageul, Pierre Ronco, Emmanuelle Plaisier
Publikováno v: American Journal of Kidney Diseases. 40:649-654
Background: Anti-glomerular basement membrane (GBM) nephritis is a rare disease induced by antibodies directed against alpha3(IV)NC1, the Goodpasture antigen. We report a patient with Crohn's disease who developed anti-GBM nephritis and the skin blis
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d91224819521937a9bf293a2442beeb3
https://doi.org/10.1053/ajkd.2002.34929
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10
Adult haemolytic and uraemic syndrome: causes and prognostic factors in the last decade
Autor: Cécile Vigneau, Marie-Alyette Costa, Jean-Daniel Sraer, Antoine Flahault, Isabelle Tostivint, Jean-Philippe Haymann, Béatrice Mougenot, Eric Rondeau
Publikováno v: Nephrology, Dialysis, Transplantation, Vol. 17, No 7 (2002) pp. 1228-34
Background. Haemolytic uraemic syndrome (HUS) is a rare and severe disease of various aetiologies in adults. The effect of fresh frozen plasma (FFP) infusion in adults suffering from HUS is not well defined. The aim of this retrospective study was to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62b42a2aca02b142c8490fe59a9c9ca9
https://doi.org/10.1093/ndt/17.7.1228
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