Primary Hyperoxaluria

by Jérôme Harambat, Sonia Fargue, Justine Bacchetta, Cécile Acquaviva, Pierre Cochat
Published 2011-01-01

Bone marrow adiposity inversely correlates with bone turnover in pediatric renal osteodystrophy

by Ornatcha Sirimongkolchaiyakul, Renata C. Pereira, Barbara Gales, Justine Bacchetta, Isidro B. Salusky, Katherine Wesseling-Perry
Published 2021-12-01

Bone Disease in Nephropathic Cystinosis: Beyond Renal Osteodystrophy

by Irma Machuca-Gayet, Thomas Quinaux, Aurélia Bertholet-Thomas, Ségolène Gaillard, Débora Claramunt-Taberner, Cécile Acquaviva-Bourdain, Justine Bacchetta
Published 2020-04-01

Hypertension in Children and Adolescents: A Position Statement From a Panel of Multidisciplinary Experts Coordinated by the French Society of Hypertension

by Béatrice Bouhanick, Philippe Sosner, Philippe Sosner, Philippe Sosner, Karine Brochard, Claire Mounier-Véhier, Geneviève Plu-Bureau, Sébastien Hascoet, Bruno Ranchin, Bruno Ranchin, Christine Pietrement, Laetitia Martinerie, Jean Marc Boivin, Jean Pierre Fauvel, Jean Pierre Fauvel, Justine Bacchetta, Justine Bacchetta
Published 2021-07-01

Antibacterial responses by peritoneal macrophages are enhanced following vitamin D supplementation.

by Justine Bacchetta, Rene F Chun, Barbara Gales, Joshua J Zaritsky, Sandrine Leroy, Katherine Wesseling-Perry, Niels Boregaard, Anjay Rastogi, Isidro B Salusky, Martin Hewison
Published 2014-01-01

A prospective case–control pilot study to evaluate bone microarchitecture in children and teenagers on long-term parenteral nutrition using HR-pQCT

by Typhaine Louazon, Pierre Poinsot, Lioara Restier, Abdelouahed Belmalih, Irène Loras-Duclaux, Stéphanie Marotte, Sophie Heissat, Didier Barnoud, Cécile Chambrier, Cyrille B. Confavreux, Alain Lachaux, Justine Bacchetta, Noel Peretti
Published 2021-04-01

Response to Cysteamine in Osteoclasts Obtained from Patients with Nephropathic Cystinosis: A Genotype/Phenotype Correlation

by Thomas Quinaux, Aurélia Bertholet-Thomas, Aude Servais, Olivia Boyer, Isabelle Vrillon, Julien Hogan, Sandrine Lemoine, Ségolène Gaillard, Candide Alioli, Sophie Vasseur, Cécile Acquaviva, Olivier Peyruchaud, Irma Machuca-Gayet, Justine Bacchetta
Published 2021-09-01

Worldwide view of nephropathic cystinosis: results from a survey from 30 countries

by Aurélia Bertholet-Thomas, Julien Berthiller, Velibor Tasic, Behrouz Kassai, Hasan Otukesh, Marcella Greco, Jochen Ehrich, Rejane de Paula Bernardes, Georges Deschênes, Sally-Ann Hulton, Michel Fischbach, Kenza Soulami, Bassam Saeed, Ehsan Valavi, Carlos Jose Cobenas, Bülent Hacihamdioglu, Gabrielle Weiler, Pierre Cochat, Justine Bacchetta
Published 2017-07-01

Determinants of Statural Growth in European Children With Chronic Kidney Disease: Findings From the Cardiovascular Comorbidity in Children With Chronic Kidney Disease (4C) Study

by Rouven Behnisch, Marietta Kirchner, Ali Anarat, Justine Bacchetta, Rukshana Shroff, Yelda Bilginer, Sevgi Mir, Salim Caliskan, Dusan Paripovic, Jerome Harambat, Francesca Mencarelli, Rainer Büscher, Klaus Arbeiter, Oguz Soylemezoglu, Ariane Zaloszyc, Aleksandra Zurowska, Anette Melk, Uwe Querfeld, Franz Schaefer, and the 4C Study Consortium
Published 2019-07-01

Markers of bone metabolism are affected by renal function and growth hormone therapy in children with chronic kidney disease.

by Anke Doyon, Dagmar-Christiane Fischer, Aysun Karabay Bayazit, Nur Canpolat, Ali Duzova, Betül Sözeri, Justine Bacchetta, Ayse Balat, Anja Büscher, Cengiz Candan, Nilgun Cakar, Osman Donmez, Jiri Dusek, Martina Heckel, Günter Klaus, Sevgi Mir, Gül Özcelik, Lale Sever, Rukshana Shroff, Enrico Vidal, Elke Wühl, Matthias Gondan, Anette Melk, Uwe Querfeld, Dieter Haffner, Franz Schaefer, 4C Study Consortium
Published 2015-01-01

The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results

by Giulia Bassanese, Tanja Wlodkowski, Aude Servais, Laurence Heidet, Dario Roccatello, Francesco Emma, Elena Levtchenko, Gema Ariceta, Justine Bacchetta, Giovambattista Capasso, Augustina Jankauskiene, Marius Miglinas, Pietro Manuel Ferraro, Giovanni Montini, Jun Oh, Stephane Decramer, Tanja Kersnik Levart, Jack Wetzels, Elisabeth Cornelissen, Olivier Devuyst, Aleksandra Zurowska, Lars Pape, Anja Buescher, Dieter Haffner, Natasa Marcun Varda, Gian Marco Ghiggeri, Giuseppe Remuzzi, Martin Konrad, Germana Longo, Detlef Bockenhauer, Atif Awan, Ilze Andersone, Jaap W. Groothoff, Franz Schaefer
Published 2021-06-01

Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome

by Christelle Arrondel, Sophia Missoury, Rozemarijn Snoek, Julie Patat, Giulia Menara, Bruno Collinet, Dominique Liger, Dominique Durand, Olivier Gribouval, Olivia Boyer, Laurine Buscara, Gaëlle Martin, Eduardo Machuca, Fabien Nevo, Ewen Lescop, Daniela A. Braun, Anne-Claire Boschat, Sylvia Sanquer, Ida Chiara Guerrera, Patrick Revy, Mélanie Parisot, Cécile Masson, Nathalie Boddaert, Marina Charbit, Stéphane Decramer, Robert Novo, Marie-Alice Macher, Bruno Ranchin, Justine Bacchetta, Audrey Laurent, Sophie Collardeau-Frachon, Albertien M. van Eerde, Friedhelm Hildebrandt, Daniella Magen, Corinne Antignac, Herman van Tilbeurgh, Géraldine Mollet
Published 2019-09-01