Zobrazeno 1 - 10 of 113 pro vyhledávání: '"Lh, Noel"'
1
Severe renal failure in acute bacterial pyelonephritis: Do not forget corticosteroids
Autor: Th, Sqalli, Hamzaoui H, Guiard E, Lh, Noel, Fadi Fakhouri
Publikováno v: Saudi Journal of Kidney Diseases and Transplantation, Vol 21, Iss 1, Pp 118-122 (2010)
Europe PubMed Central
Acute renal failure (ARF) is a rare complication of acute pyelonephritis in adult immunocompetent patients. Recovery of renal function usually occurs if antibiotics are promptly initiated. However, long-term consequences of renal scarring due to acut
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::350b455cff02312d3416c822f0133322
http://www.sjkdt.org/article.asp?issn=1319-2442
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2
Persistence of antineutrophil cytoplasmic antibodies (ANCA) in asymptomatic patients with systemic polyarteritis nodosa or Churg-Strauss syndrome: follow-up of 53 patients
Autor: Cohen P, Guillevin L, Laurence Baril, Lhote F, Lh, Noel, Lesavre P
Publikováno v: Scopus-Elsevier
Europe PubMed Central
We retrospectively analyzed the significance of persistent ANCA positivity after clinical remission in 53 consecutive patients with histologically and/or angiographically proven polyarteritis nodosa (PAN), or Churg-Strauss syndrome (CSS) followed bet
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c469e79183b2471aa5d3cf474d3b6e44
https://pubmed.ncbi.nlm.nih.gov/7656465
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5
Akademický článek
Dissecting the histological features of lupus nephritis highlights new common patterns of injury in class III/IV.
Autor: Bolognesi MM; Pathology, Department of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy maddalena.bolognesi@unimib.it., Capitoli G; Bicocca Bioinformatics Biostatistics and Bioimaging B4 Center, Department of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy., Galimberti S; Bicocca Bioinformatics Biostatistics and Bioimaging B4 Center, Department of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy., Cattoretti G; Pathology, Department of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy.; Pathology Department, ASST Monza - San Gerardo Hospital, Monza, Italy., Bajema I; Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands., Bruijn JA; Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands., Cook HT; Department for Immunology and Inflammation, Centre for Inflammatory Disease, Imperial College London, London, UK., Noel LH; Department of Pathology, Necker Hospital, Paris, France., Pagni F; Pathology, Department of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy.; Pathology Department, ASST Monza - San Gerardo Hospital, Monza, Italy., Ferrario F; Pathology Department, ASST Monza - San Gerardo Hospital, Monza, Italy., Wester Trejo M; Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands., L'Imperio V; Pathology, Department of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy.; Pathology Department, ASST Monza - San Gerardo Hospital, Monza, Italy.
Publikováno v: Annals of the rheumatic diseases [Ann Rheum Dis] 2022 Dec; Vol. 81 (12), pp. 1704-1711. Date of Electronic Publication: 2022 Aug 08.
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6
Akademický článek
The clinicopathologic characteristics of kidney diseases related to monotypic IgA deposits.
Autor: Vignon M; Department of Nephrology, Hôpital Necker Enfants Malades, Université Paris Descartes, Paris, France. Electronic address: marguerite.vignon@aphp.fr., Cohen C; Department of Nephrology, Hôpital Necker Enfants Malades, Université Paris Descartes, Paris, France., Faguer S; Department of Nephrology, CHU Rangueil, Toulouse, France., Noel LH; Department of Pathology, Hôpital Necker Enfants Malades, Université Paris Descartes, Paris, France., Guilbeau C; Department of Pathology, CHU Rangueil, Toulouse, France., Rabant M; Department of Pathology, Hôpital Necker Enfants Malades, Université Paris Descartes, Paris, France., Higgins S; Department of Pathology, Hôpital Necker Enfants Malades, Université Paris Descartes, Paris, France., Hummel A; Department of Nephrology, Hôpital Necker Enfants Malades, Université Paris Descartes, Paris, France., Hertig A; Department of Nephrology, Hôpital Tenon, Université Pierre et Marie Curie, Paris, France., Francois H; Department of Nephrology, CHU de Bicêtre, Université Paris Sud, Bicêtre, France., Lequintrec M; Department of Nephrology, CHU de Montpellier, Montpellier, France., Vilaine E; Department of Nephrology, CHU Ambroise Paré, Université de Versailles Saint-Quentin-en-Yvelines, Boulogne, France., Knebelmann B; Department of Nephrology, Hôpital Necker Enfants Malades, Université Paris Descartes, Paris, France., Pourrat J; Department of Nephrology, CHU Rangueil, Toulouse, France., Chauveau D; Department of Nephrology, CHU Rangueil, Toulouse, France., Goujon JM; Departments of Pathology and Ultrastructural Pathology, CHU Poitiers, Centre de référence maladies rares amylose AL et autres maladies par dépôts d'immunoglobulines monoclonales, Poitiers, France., Javaugue V; Department of Nephrology, CHU Poitiers, Centre de référence maladies rares amylose AL et autres maladies par dépôts d'immunoglobulines monoclonales, Poitiers, France., Touchard G; Departments of Pathology and Ultrastructural Pathology, CHU Poitiers, Centre de référence maladies rares amylose AL et autres maladies par dépôts d'immunoglobulines monoclonales, Poitiers, France; Department of Nephrology, CHU Poitiers, Centre de référence maladies rares amylose AL et autres maladies par dépôts d'immunoglobulines monoclonales, Poitiers, France., El Karoui K; Department of Nephrology, Hôpital Henri Mondor, Université Paris Est, Créteil, France., Bridoux F; Department of Nephrology, CHU Poitiers, Centre de référence maladies rares amylose AL et autres maladies par dépôts d'immunoglobulines monoclonales, Poitiers, France; Department of Immunology, National Center for Scientific Research, Joint Research Unit 7276, University of Limoges, Centre de référence maladies rares amylose AL et autres maladies par dépôts d'immunoglobulines monoclonales, Limoges, France.
Publikováno v: Kidney international [Kidney Int] 2017 Mar; Vol. 91 (3), pp. 720-728. Date of Electronic Publication: 2017 Jan 06.
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7
Akademický článek
Pauci-immune crescentic glomerulonephritis without ANCA in a patient presenting with Candida parapsilosis endocarditis.
Autor: Scemla A; Service des maladies infectieuses et tropicales, centre d'infectiologie Necker-Pasteur, IHU Imagine, université Paris Descartes, AP-HP, 75743 Paris cedex 15, France., Charlier C; Service des maladies infectieuses et tropicales, centre d'infectiologie Necker-Pasteur, IHU Imagine, université Paris Descartes, AP-HP, 75743 Paris cedex 15, France. Electronic address: caroline.charlier@aphp.fr., Noel LH; Service d'anatomopathologie, hôpital Necker, Paris, France., Amazzough K; Service des maladies infectieuses et tropicales, centre d'infectiologie Necker-Pasteur, IHU Imagine, université Paris Descartes, AP-HP, 75743 Paris cedex 15, France., Von Rosen FT; Service des maladies infectieuses et tropicales, centre d'infectiologie Necker-Pasteur, IHU Imagine, université Paris Descartes, AP-HP, 75743 Paris cedex 15, France., Lesavre P; Service de néphrologie, hôpital Necker, Paris, France., Lortholary O; Service des maladies infectieuses et tropicales, centre d'infectiologie Necker-Pasteur, IHU Imagine, université Paris Descartes, AP-HP, 75743 Paris cedex 15, France.
Publikováno v: Medecine et maladies infectieuses [Med Mal Infect] 2016 May; Vol. 46 (3), pp. 163-5. Date of Electronic Publication: 2016 Feb 17.
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8
Akademický článek
Light and heavy chain deposition disease associated with CH1 deletion.
Autor: Cohen C; Service de néphrologie , hôpital Necker , Paris , France., El-Karoui K; Service de néphrologie , hôpital Necker , Paris , France., Alyanakian MA; Service d'immunologie , hôpital Necker , Paris , France., Noel LH; Service d'anatomo-pathologie , hôpital Necker , Paris , France., Bridoux F; Service de néphrologie , CHU Poitiers , Poitiers , France., Knebelmann B; Service de néphrologie , hôpital Necker , Paris , France.
Publikováno v: Clinical kidney journal [Clin Kidney J] 2015 Apr; Vol. 8 (2), pp. 237-9. Date of Electronic Publication: 2015 Jan 28.
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9
Akademický článek
Improving mutation screening in familial hematuric nephropathies through next generation sequencing.
Autor: Morinière V; Departments of Genetics, and Assistance Publique des Hôpitaux de Paris, Reference Center for Renal Hereditary Disease for Children and Adults (MARHEA), Paris, France;, Dahan K; Department of Genetics, Institute of Pathology and Genetics, Gosselies, Belgium;, Hilbert P; Department of Genetics, Institute of Pathology and Genetics, Gosselies, Belgium;, Lison M; Department of Genetics, Institute of Pathology and Genetics, Gosselies, Belgium;, Lebbah S; Assistance Publique des Hôpitaux de Paris, Reference Center for Renal Hereditary Disease for Children and Adults (MARHEA), Paris, France;, Topa A; Department of Clinical Genetics, Sahlgrenska University Hospital, Gothenburg, Sweden;, Bole-Feysot C; Genomics Platform, Imagine Institute, Paris, France;, Pruvost S; Genomics Platform, Imagine Institute, Paris, France;, Nitschke P; Bioinformatics Platform, Paris Descartes-Sorbonne Paris Cité University, Paris, France;, Plaisier E; Assistance Publique des Hôpitaux de Paris, Nephrology Service, Tenon Hospital, Paris, France;, Knebelmann B; Nephrology Service and., Macher MA; Assistance Publique des Hôpitaux de Paris, Pediatric Nephrology Service, Robert Debré Hospital, Paris, France; and., Noel LH; Pathology, and., Gubler MC; Institut National de la Santé et de la Recherche Médicale, Inserm UMR 1163, Laboratory of Inherited Kidney Diseases, Imagine Institute, Paris, France., Antignac C; Departments of Genetics, and Assistance Publique des Hôpitaux de Paris, Reference Center for Renal Hereditary Disease for Children and Adults (MARHEA), Paris, France; Institut National de la Santé et de la Recherche Médicale, Inserm UMR 1163, Laboratory of Inherited Kidney Diseases, Imagine Institute, Paris, France Paris Descartes-Sorbonne Paris Cité University, and corinne.antignac@inserm.fr., Heidet L; Assistance Publique des Hôpitaux de Paris, Reference Center for Renal Hereditary Disease for Children and Adults (MARHEA), Paris, France; Pediatric Nephrology Service, Assistance Publique des Hôpitaux de Paris, Necker-Enfants Malades Hospital, Paris, France;
Publikováno v: Journal of the American Society of Nephrology : JASN [J Am Soc Nephrol] 2014 Dec; Vol. 25 (12), pp. 2740-51. Date of Electronic Publication: 2014 May 22.
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10
Akademický článek
A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS.
Autor: Huynh Cong E; INSERM U1163, Laboratory of Hereditary Kidney Diseases, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France;, Bizet AA; INSERM U1163, Laboratory of Hereditary Kidney Diseases, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France;, Boyer O; INSERM U1163, Laboratory of Hereditary Kidney Diseases, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France; Assistance Publique-Hôpitaux de Paris, Department of Pediatric Nephrology, Necker Hospital, Paris, France;, Woerner S; INSERM U1163, Laboratory of Hereditary Kidney Diseases, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France;, Gribouval O; INSERM U1163, Laboratory of Hereditary Kidney Diseases, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France;, Filhol E; INSERM U1163, Laboratory of Hereditary Kidney Diseases, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France;, Arrondel C; INSERM U1163, Laboratory of Hereditary Kidney Diseases, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France;, Thomas S; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France; INSERM U1163, Laboratory of Embryology and Genetics of Congenital Malformations, Paris, France;, Silbermann F; INSERM U1163, Laboratory of Hereditary Kidney Diseases, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France;, Canaud G; Assistance Publique-Hôpitaux de Paris, Department of Nephrology and Transplantation and Intensive Care Unit, Necker Hospital, Paris, France;, Hachicha J; Department of Nephrology, University of Sfax, Hedi Chaker Hospital, Sfax, Tunisia;, Ben Dhia N; Department of Nephrology, Faculty of Medicine, Monastir, Tunisia;, Peraldi MN; INSERM U940, Paris Diderot University and Nephrology Unit, Saint-Louis Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France;, Harzallah K; Faculty of Medicine, Military Hospital of Tunis, Tunis, Tunisia;, Iftene D; Department of Nephrology-Dialysis, Army Central Hospital, Kouba, Alger, Algeria;, Daniel L; Assistance Publique-Hôpitaux de Marseille, Department of Pathology, la Timone Hospital, Marseille, France;, Willems M; INSERM U844, Department of Medical Genetics, Arnaud de Villeneuve Hospital, Montpellier, France;, Noel LH; Assistance Publique-Hôpitaux de Paris, Department of Nephrology and Transplantation and Intensive Care Unit, Necker Hospital, Paris, France;, Bole-Feysot C; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France; Imagine Institute, Genomic Core Facility, Paris, France;, Nitschké P; Paris-Descartes Sorbonne Paris-Cité University, Bioinformatics Core Facility, Paris, France., Gubler MC; INSERM U1163, Laboratory of Hereditary Kidney Diseases, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France;, Mollet G; INSERM U1163, Laboratory of Hereditary Kidney Diseases, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France;, Saunier S; INSERM U1163, Laboratory of Hereditary Kidney Diseases, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France;, Antignac C; INSERM U1163, Laboratory of Hereditary Kidney Diseases, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France; Assistance Publique-Hôpitaux de Paris, Department of Genetics, Necker Hospital, Paris, France; corinne.antignac@inserm.fr.
Publikováno v: Journal of the American Society of Nephrology : JASN [J Am Soc Nephrol] 2014 Nov; Vol. 25 (11), pp. 2435-43. Date of Electronic Publication: 2014 May 29.
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