Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Flavio Bandin"'
Autor:
Aymeric Dallocchio, Flavio Bandin, Brigitte Llanas, L. Ichay, Astrid Godron, Stéphane Bouchet, Peggy Gandia, F Saint-marcoux, Vincent Guigonis, Jérôme Harambat, Karine Brochard, Stéphane Decramer, Denis Morin, Pierre Marquet, Stéphanie Tellier
Publikováno v:
Clinical Journal of the American Society of Nephrology. 11:1777-1782
Background and objectives Therapeutic drug monitoring of mycophenolic acid can improve clinical outcome in organ transplantation and lupus, but data are scarce in idiopathic nephrotic syndrome. The aim of our study was to investigate whether mycophen
Autor:
Stanislas Faguer, Dominique Chauveau, Antoine Huart, Joost P. Schanstra, Nicolas Chassaing, Flavio Bandin, Audrey Casemayou, Patrick Calvas, Stéphane Decramer, Arnaud Garnier, Cathie Prouheze
Publikováno v:
Kidney International
Kidney International, 2014, 86 (5), pp.1007-1015. ⟨10.1038/ki.2014.202⟩
Kidney International, Nature Publishing Group, 2014, 86 (5), pp.1007-1015. ⟨10.1038/ki.2014.202⟩
Kidney International, 2014, 86 (5), pp.1007-1015. ⟨10.1038/ki.2014.202⟩
Kidney International, Nature Publishing Group, 2014, 86 (5), pp.1007-1015. ⟨10.1038/ki.2014.202⟩
International audience; HNF1B-related disease is an emerging condition characterized by an autosomal-dominant inheritance, a 50% rate of de novo mutations, and a highly variable phenotype (renal involvement, maturity-onset diabetes of the young type
Autor:
Vincent Guigonis, Nicolas Chassaing, Stanislas Faguer, Stéphane Decramer, Flavio Bandin, Dominique Chauveau
Publikováno v:
Néphrologie & Thérapeutique. 9:393-397
HNF1B encodes for a transcription factor involved in the early development of the kidney, pancreas, liver and genital tract. Mutations in HNF1B are dominantly inherited and consist of whole-gene deletion, or small mutation. De novo mutation occurs in
Autor:
Stéphanie Tellier, Stéphane Decramer, Arnaud Garnier, Brigitte Llanas, Aurélia Bertholet-Thomas, Sylvie Nathanson, Flavio Bandin, Mathilde Cailliez, Vincent Guigonis, Christine Pietrement, Olivier Dunand, L. Ichay, Karine Brochard
Publikováno v:
Pediatric Nephrology. 28:911-918
Rituximab (RTX) has recently showed promising results in the treatment of steroid-dependent idiopathic nephrotic syndrome (SDNS).This was a retrospective multicenter study of 18 children treated with RTX for SDNS, with a mean follow-up of 3.2 years.
Autor:
Christine Azema, Flavio Bandin, Renata Vitkevic, Hala Wannous, Isabelle Brocheriou, Patrice Callard, Tim Ulinski, Stéphane Decramer, Bilal Aoun
Publikováno v:
Pediatric Nephrology. 28:493-498
Protocol biopsies can detect subclinical rejection and early signs of calcineurin inhibitor-induced nephrotoxicity.In a prospective study, protocol biopsies 3 and 12 months after transplant in transplanted children from two centers were studied. One
Autor:
Stéphane Decramer, Justyna Siwy, Joost P. Schanstra, Harald Mischak, Benjamin Breuil, Flavio Bandin, Jean-Loup Bascands
Publikováno v:
Journal of Urology
Journal of Urology, 2012, 187 (3), pp.1006-11. ⟨10.1016/j.juro.2011.10.169⟩
Journal of Urology, Elsevier, 2012, 187 (3), pp.1006-11. ⟨10.1016/j.juro.2011.10.169⟩
Journal of Urology, 2012, 187 (3), pp.1006-11. ⟨10.1016/j.juro.2011.10.169⟩
Journal of Urology, Elsevier, 2012, 187 (3), pp.1006-11. ⟨10.1016/j.juro.2011.10.169⟩
International audience; PURPOSE: Severe ureteropelvic junction obstruction is treated surgically. However, for milder cases most clinical teams adopt a watchful waiting approach and only operate in the presence of significant decline of renal functio
Autor:
Nicolas Chassaing, Stanislas Faguer, Stéphane Decramer, Benoit Arveiler, Dominique Chauveau, Patrick Calvas, Flavio Bandin, Marie-Béatrice Nogier, Cathie Prouheze, Caroline Rooryck
Publikováno v:
European Journal of Medical Genetics. 54:e437-e440
Chromosomal imbalance of the 17q12 region (which includes the HNF1B transcription factor) has recently emerged as a frequent condition. 17q12 deletion was found in patients with various renal abnormalities, diabetes mellitus (MODY type 5), genital tr
Autor:
Cécile Caubet, Jean-Loup Bascands, Mathieu Miravete, Rana Chaaya, Julien Gonzalez, Bénédicte Buffin-Meyer, Joost P. Schanstra, Stéphane Decramer, Julie Klein, Flavio Bandin
Publikováno v:
International Journal of Experimental Pathology. 92:168-192
Ureteropelvic junction (UPJ) obstruction is the most frequently observed cause of obstructive nephropathy in children. Neonatal and foetal animal models have been developed that mimic closely what is observed in human disease. The purpose of this rev
Autor:
Gérard Champion, Muriel Brun, Tim Ulinski, Guylhène Bourdat-Michel, Emma Allain Launay, Bruno Ranchin, Jérôme Harambat, Marina Charbit, Georges Deschênes, Monique Elmaleh, Christine Pietrement, Sylvie Nathanson, Flavio Bandin, Theresa Kwon, Sylvie Cloarec
Publikováno v:
Clinical Journal of the American Society of Nephrology. 5:1218-1228
Background and objectives: Neurologic involvement is the most threatening complication of diarrhea-associated hemolytic uremic syndrome (D+HUS). Design, setting, participants, & measurements: We report a retrospective multicenter series of 52 patient
Autor:
Joao-Bosco Pesquero, David J. Salant, Stéphane Decramer, Eric Neau, J.P. Schanstra, Julie Klein, Peter Heeringa, Flavio Bandin, Jean-Loup Bascands, Julien Gonzalez
Publikováno v:
Journal of the American Society of Nephrology, 21(7), 1157-1164. AMER SOC NEPHROLOGY
Journal of the American Society of Nephrology
Journal of the American Society of Nephrology, 2010, 21 (7), pp.1157-64. ⟨10.1681/ASN.2009090887⟩
Journal of the American Society of Nephrology
Journal of the American Society of Nephrology, 2010, 21 (7), pp.1157-64. ⟨10.1681/ASN.2009090887⟩
International audience; Severe inflammation characterizes rapidly progressive glomerulonephritides, and expression of the kinin B1 receptor (B1R) associates with inflammation. Delayed B1R blockade reduces renal inflammation in a model of unilateral u