Výsledky vyhledávání - "Jean-Claude Davin"

A randomized clinical trial indicates that levamisole increases the time to relapse in children with steroid-sensitive idiopathic nephrotic syndrome

Autor: Jean-Claude Davin, Mariken P. Gruppen, Ashima Gulati, Elisabeth A.M. Cornelissen, Antonia H. Bouts, Laura Massella, Maria Van Dyck, Aleksandra Zurowska, Marijke C. Jansen-van der Weide, Michał Maternik, Maruschka P. Merkus, Arvind Bagga, Johan Vande Walle, Patrick Niaudet, Ann Raes, Thierry Schurmans, Francesco Emma

Publikováno v: Kidney international, 93 (2
KIDNEY INTERNATIONAL
Kidney international, 93(2), 510-518. Nature Publishing Group
Kidney International, 93, 510-518
Kidney International, 93, 2, pp. 510-518

Levamisole has been considered the least toxic and least expensive steroid-sparing drug for preventing relapses of steroid-sensitive idiopathic nephrotic syndrome (SSINS). However, evidence for this is limited as previous randomized clinical trials w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::837fc8be0c1669afb2bba4f017ef69fc
https://doi.org/10.1016/j.kint.2017.08.011

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Eculizumab in Pediatric Dense Deposit Disease

Autor: Sandrine Florquin, Bernd Hoppe, Pietrik J. Schriemer, Michiel J. S. Oosterveld, Jaap W. Groothoff, Jean-Claude Davin, L.P.W.J. van den Heuvel, Mark R. Garrelfs, Kerstin Amann, Antonia H. M. Bouts, Joris J. T. H. Roelofs

Publikováno v: Clinical Journal of the American Society of Nephrology, 10, 1773-1782
Clinical journal of the American Society of Nephrology, 10(10), 1773-1782. American Society of Nephrology
Clinical Journal of the American Society of Nephrology, 10, 10, pp. 1773-1782

Dense deposit disease (DDD), a subtype of C3 glomerulopathy, is a rare disease affecting mostly children. Treatment options are limited. Debate exists whether eculizumab, a monoclonal antibody against complement factor C5, is effective in DDD. Report

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85993f84895b27201e04a1a9f32dd5bf
https://doi.org/10.2215/cjn.01360215

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The difficulty in considering modifiable pathology risk factors in children with IgA nephropathy: crescents and timing of renal biopsy

Autor: Rosanna Coppo, Jean-Claude Davin

Publikováno v: Pediatric nephrology (Berlin, Germany), 30(2), 189-192. Springer Verlag

The need for an early diagnosis of primary IgA nephropathy (IgAN) is particularly felt in children since they have a long life expectancy. However, IgAN has a slowly progressive course and renal function can even remain unchanged for decades. The lon

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::558bee344c4c21f01ddfb1bedd101108
https://doi.org/10.1007/s00467-014-2954-9

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Henoch-Schönlein purpura nephritis in children

Autor: Jean-Claude Davin, Rosanna Coppo

Publikováno v: Nature reviews. Nephrology. 10(10):563-573

Nephritis is observed in around 30% of children with Henoch–Schonlein purpura (HSP). The treatment of these patients is complicated by similarity to IgA nephropathy. Here, the authors discuss advances in understanding of the pathophysiology, diagno

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b45b752bb5afdaa559334420e56885a
https://doi.org/10.1038/nrneph.2014.126

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Pitfalls in recommending evidence-based guidelines for a protean disease like Henoch-Schönlein purpura nephritis

Autor: Rosanna Coppo, Jean-Claude Davin

Publikováno v: Pediatric nephrology (Berlin, Germany), 28(10), 1897-1903. Springer Verlag

The long-term prognosis of Henoch–Schonlein purpura nephritis (HSPN) depends on the severity of initial clinical symptoms and histological features [1, 2]. The risk of evolution into a chronic kidney disease (CKD) may be as high as 50, 40 and 15 %

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3022db651f6c2dbf20f535e3d5e0d3e
https://doi.org/10.1007/s00467-013-2550-4

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Prevention of steroid-induced low bone mineral density * in children with renal diseases: a systematic review

Autor: Antonia H. M. Bouts, Mariken P. Gruppen, Michiel F. Schreuder, Jean-Claude Davin, Michiel J. S. Oosterveld, Eiske M. Dorresteijn, Sharon P. Kramer

Publikováno v: Nephrology Dialysis Transplantation, 28, 2099-2106. Oxford University Press
Nephrology, Dialysis, Transplantation, 28, 2099-106
Nephrology, Dialysis, Transplantation, 28, 8, pp. 2099-106

Item does not contain fulltext BACKGROUND: Children with renal diseases who are treated with glucocorticoids are at increased risk of developing osteoporosis and fractures. However, there is no common strategy for prevention of corticosteroid-induced

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::441a790a7020e8a30ec9e5fb0239703c
https://hdl.handle.net/2066/186655

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The glomerular permeability factors in idiopathic nephrotic syndrome

Autor: Jean-Claude Davin

Publikováno v: Pediatric nephrology, 31 (2
Pediatric Nephrology (Berlin, Germany)

It is currently postulated that steroid-sensitive idiopathic nephrotic syndrome (SSNS) and steroid-resistant idiopathic nephrotic syndrome (SRNS), which are not related to the mutation of a gene coding for podocyte structures or for glomerular baseme

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d491310f313f547c82a7e95726e3355c
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/253386

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Henoch-Schonlein Purpura Nephritis: Pathophysiology, Treatment, and Future Strategy

Autor: Jean-Claude Davin

Publikováno v: American Society of Nephrology. Clinical Journal, 6 (3

Henoch-Schönlein purpura nephritis is a rare kidney disease leading to chronic kidney disease in a non-negligible percentage of patients. Although retrospective studies suggest beneficial effects of some therapies, prospective randomized clinical tr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::177fa578f55bbf9d709e2ceab9578bc0
https://doi.org/10.2215/cjn.06710810

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Non-atheromatous arterial stenoses in atypical haemolytic uraemic syndrome associated with complement dysregulation

Autor: Chantal Loirat, Monique Elmaleh-Bergès, Raphaël Blanc, Jacques Moret, Charles Majoie, Theresa Kwon, Véronique Frémeaux-Bacchi, Georges Deschênes, Timothy H.J. Goodship, Marie-Alice Macher, Jean-Claude Davin, Julien Savatovsky

Publikováno v: Nephrology, dialysis, transplantation, 25(10), 3421-3425. Oxford University Press

Background. A child, who presented atypical haemolytic uraemic syndrome (aHUS) at the age of 1 month, developed cerebral ischaemic events at the age of 10 years. Results. Stenoses of both carotid arteries, left subclavian and vertebral arteries, seve

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::395ffcbbffb1f58daa410cfda3d16cce
https://doi.org/10.1093/ndt/gfq319

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Maintenance of Kidney Function Following Treatment With Eculizumab and Discontinuation of Plasma Exchange After a Third Kidney Transplant for Atypical Hemolytic Uremic Syndrome Associated With a CFH Mutation

Autor: Antonia H. Bouts, Jaap W. Groothoff, Jean-Claude Davin, Valentina Gracchi, Lisa Strain, Timothy H.J. Goodship

Publikováno v: American journal of kidney diseases, 55(4), 708-711. W.B. Saunders Ltd

Kidney transplant in patients with atypical hemolytic uremic syndrome (aHUS) is associated with a poor outcome because of recurrent disease, especially in patients known to have a factor H mutation. Long-term prophylactic plasma exchange and combined

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4abc6edf1c16ed39296467f5cc98643
https://doi.org/10.1053/j.ajkd.2009.08.011

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