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Laure-Hélène Noël

Researcher at Necker-Enfants Malades Hospital

Publications -  241
Citations -  13955

Laure-Hélène Noël is an academic researcher from Necker-Enfants Malades Hospital. The author has contributed to research in topics: Kidney & Glomerulonephritis. The author has an hindex of 61, co-authored 241 publications receiving 12042 citations. Previous affiliations of Laure-Hélène Noël include Centre national de la recherche scientifique & Paris Descartes University.

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Case report and literature review: Glomerular and neurologic thrombotic microangiopathy as a primary manifestation of multicentric castleman disease.

Adrien Flahault, +8 more
- 01 Oct 2016 - 
TL;DR: Although rare, this diagnosis is worth knowing, as specific treatment has to be started as soon as possible and proved to be efficient in this case as well as in other reports in the literature.
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Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies

Aude Servais, +20 more
- 02 Aug 2012 - 
TL;DR: A critical role of fluid-phase alternative pathway dysregulation in the pathogenesis of C3 glomerulopathies as well as in immune complex-mediated glomerular diseases is suggested.
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Clinical spectrum associated with hepatocyte nuclear factor-1β mutations

Christine Bellanné-Chantelot, +10 more
- 06 Apr 2004 - 
TL;DR: Detailed phenotypic analysis underlines the systemic spectrum of the disease and its wide variability, leading to different modes of presentation, and confirms that MODY5 may occur because of de novo mutation in HNF-1.
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Polyarteritis nodosa related to hepatitis B virus. A prospective study with long-term observation of 41 patients.

Loïc Guillevin, +7 more
- 01 Sep 1995 - 
TL;DR: This protocol is proposed as the first treatment for HBV-related PAN, because it surpasses the conventional treatment with corticosteroids and cyclophosphamide, which facilitates viral replication and the development of chronic HBV infection.
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C3 glomerulopathy: a new classification

Fadi Fakhouri, +4 more
- 06 Jul 2010 - 
TL;DR: It is suggested that glomerular pathologies that are characterized by the isolated deposition of C3 could usefully be classified by the term C3 glomerulopathy, and this classification would alert the pathologist and nephrologist to the importance of screening for acquired and genetic abnormalities in complement regulation.