Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Caroline Galeotti"'
Autor:
Isabelle Touitou, Sophie Georgin-Lavialle, Linda Rossi-Semerano, Caroline Galeotti, Bilade Cherqaoui, Véronique Hentgen, P. Dusser, Isabelle Koné-Paut, Maryam Piram
Publikováno v:
Revue du Rhumatisme
Revue du Rhumatisme, Elsevier, 2019, 86, pp.504-510. ⟨10.1016/j.rhum.2019.06.006⟩
Revue du Rhumatisme, Elsevier, 2019, 86, pp.504-510. ⟨10.1016/j.rhum.2019.06.006⟩
Resume Objectifs La fievre mediterraneenne familiale peut se presenter sous la forme d’atteintes musculo-squelettiques, ce qui peut la rendre difficile a differencier d'une spondylarthrite juvenile. La survenue conjointe des deux pathologies etant
Autor:
Isabelle Touitou, Véronique Hentgen, Isabelle Koné-Paut, P. Dusser, Maryam Piram, Sophie Georgin-Lavialle, Linda Rossi-Semerano, Caroline Galeotti, Bilade Cherqaoui
Publikováno v:
Joint Bone Spine
Joint Bone Spine, Elsevier Masson, 2018, ⟨10.1016/j.jbspin.2018.01.010⟩
Joint Bone Spine, Elsevier Masson, 2018, ⟨10.1016/j.jbspin.2018.01.010⟩
Children with Familial Mediterranean fever may suffer from musculoskeletal involvement, somewhat difficult to distinguish from juvenile spondyloarthritis. The association of these two diseases has been scarcely reported in children. Objective of this
Autor:
Kumaran Deiva, A.C. Desbois, Maryam Piram, Stéphane Barete, B. Wechsler, David Saadoun, Caroline Galeotti, Bahram Bodaghi, Nicolas Noel, Tu-Anh Tran, Isabelle Koné-Paut, Gilles Kaplanski, Alfred Mahr, Julien Gaudric
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 2021, 16 (S1), pp.352. ⟨10.1186/s13023-020-01620-4⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2021, 16 (S1), pp.352. ⟨10.1186/s13023-020-01620-4⟩
Orphanet Journal of Rare Diseases, Vol 16, Iss S1, Pp 1-28 (2021)
Orphanet Journal of Rare Diseases, 2021, 16 (S1), pp.352. ⟨10.1186/s13023-020-01620-4⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2021, 16 (S1), pp.352. ⟨10.1186/s13023-020-01620-4⟩
Orphanet Journal of Rare Diseases, Vol 16, Iss S1, Pp 1-28 (2021)
Behçet’s disease (BD) is a systemic variable vessel vasculitis that involves the skin, mucosa, joints, eyes, arteries, veins, nervous system and gastrointestinal system, presenting with remissions and exacerbations. It is a multifactorial disease,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::277718894c52e28abdd55b208639cb61
https://hal.sorbonne-universite.fr/hal-03152380
https://hal.sorbonne-universite.fr/hal-03152380
Autor:
Michael Hofer, Marc Delord, Pascal Pillet, Aurélia Carbasse, Sophie Georgin-Lavialle, Caroline Galeotti, Véronique Hentgen, Anne Pagnier, Gilles Grateau, Isabelle Koné-Paut, Alexandre Belot
Publikováno v:
Frontiers in Pharmacology
Frontiers in Pharmacology, Frontiers, 2021, 11, pp.568865. ⟨10.3389/fphar.2020.568865⟩
Frontiers in Pharmacology, 2021, 11, pp.568865. ⟨10.3389/fphar.2020.568865⟩
Frontiers in Pharmacology, Vol 11 (2021)
Frontiers in Pharmacology, Frontiers, 2021, 11, pp.568865. ⟨10.3389/fphar.2020.568865⟩
Frontiers in Pharmacology, 2021, 11, pp.568865. ⟨10.3389/fphar.2020.568865⟩
Frontiers in Pharmacology, Vol 11 (2021)
Objectives: The major role of interleukin (IL)-1 in the pathogenesis of hereditary recurrent fever syndromes favored the employment of targeted therapies modulating IL-1 signaling. However the best use of IL1 inhibitors in terms of dosage is difficul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74f3d779a1d276696331228262b995e0
https://hal.sorbonne-universite.fr/hal-03125751/document
https://hal.sorbonne-universite.fr/hal-03125751/document
Autor:
Alexandre Belot, Gillian I Rice, Sulliman Ommar Omarjee, Quentin Rouchon, Eve M D Smith, Marion Moreews, Maud Tusseau, Cécile Frachette, Raphael Bournhonesque, Nicole Thielens, Christine Gaboriaud, Isabelle Rouvet, Emilie Chopin, Akihiro Hoshino, Sylvain Latour, Bruno Ranchin, Rolando Cimaz, Paula Romagnani, Christophe Malcus, Nicole Fabien, Marie-Nathalie Sarda, Behrouz Kassai, Jean-Christophe Lega, Stéphane Decramer, Pauline Abou-Jaoude, Ian N Bruce, Thomas Simonet, Claire Bardel, Pierre Antoine Rollat-Farnier, Sebastien Viel, Héloise Reumaux, James O'Sullivan, Thierry Walzer, Anne-Laure Mathieu, Gaelle Marenne, Thomas Ludwig, Emmanuelle Genin, Jamie Ellingford, Brigitte Bader-Meunier, Tracy A Briggs, Michael W Beresford, Yanick J Crow, Dominique Campion, Jean-Francois Dartigues, Jean-François Deleuze, Jean-Charles Lambert, Richard Redon, Emma Allain-Launay, Kenza Bouayed, Stephane Burtey, Aurélia Carbasse, Véronique Despert, Olivier Fain, Michel Fischbach, Hugues Flodrops, Caroline Galeotti, Eric Hachulla, Yves Hatchuel, Jean-Francois Kleinmann, Isabelle Kone-Paut, Aurélia Lanteri, Irène Lemelle, Hélène Maillard, François Maurier, Ulrich Meinzer, Isabelle Melki, Sandrine Morell-Dubois, Anne Pagnier, Maryam Piram, Charlotte Samaille, Jean Sibilia, Olivia Weill, Eslam Al-Abadi, Kate Armon, Kathryn Bailey, Michael Beresford, Mary Brennan, Coziana Ciurtin, Janet Gardner-Medwin, Kirsty Haslam, Daniel Hawley, Alice Leahy, Valentina Leone, Devesh Mewar, Rob Moots, Clarissa Pilkington, Athimalaipet Ramanan, Satyapal Rangaraj, Annie Ratcliffe, Philip Riley, Ethan Sen, Arani Sridhar, Nick Wilkinson, Fiona Wood
Publikováno v:
The Lancet Rheumatology
The Lancet Rheumatology, Elsevier, 2020, 2 (2), pp.e99-e109. ⟨10.1016/S2665-9913(19)30142-0⟩
The Lancet Rheumatology, 2020, 2 (2), pp.e99-e109. ⟨10.1016/S2665-9913(19)30142-0⟩
Belot, A, Rice, G I, Ommar Omarjee, S, Rouchon, Q, Smith, E MD, Moreews, M, Tusseau, M, Frachette, C, Bournhonesque, R, Thielens, N, Gaboriaud, C, Rouvet, I, Chopin, E, Hoshino, A, Latour, S, Ranchin, B, Cimaz, R, Romagnani, P, Malcus, C, Fabien, N, Sarda, M N, Kassai, B, Lega, J-C, Decramer, S, Aboujaoude, P, Bruce, I N, Simonet, T, Bardel, C, Rollat-Farnier, P A, Sebastien, V, Reumaux, H, O'Sullivan, J, Walzer, T, Mathieu, A-L, Marenne, G, Ludwig, T, Genin, E, Ellingford, J M, Bader-Meunier, B, Briggs, T A, Beresford, M W & Crow, Y J 2020, ' Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts ', The Lancet Rheumatology . https://doi.org/10.1016/S2665-9913(19)30142-0
The Lancet Rheumatology, Elsevier, 2020, 2 (2), pp.e99-e109. ⟨10.1016/S2665-9913(19)30142-0⟩
The Lancet Rheumatology, 2020, 2 (2), pp.e99-e109. ⟨10.1016/S2665-9913(19)30142-0⟩
Belot, A, Rice, G I, Ommar Omarjee, S, Rouchon, Q, Smith, E MD, Moreews, M, Tusseau, M, Frachette, C, Bournhonesque, R, Thielens, N, Gaboriaud, C, Rouvet, I, Chopin, E, Hoshino, A, Latour, S, Ranchin, B, Cimaz, R, Romagnani, P, Malcus, C, Fabien, N, Sarda, M N, Kassai, B, Lega, J-C, Decramer, S, Aboujaoude, P, Bruce, I N, Simonet, T, Bardel, C, Rollat-Farnier, P A, Sebastien, V, Reumaux, H, O'Sullivan, J, Walzer, T, Mathieu, A-L, Marenne, G, Ludwig, T, Genin, E, Ellingford, J M, Bader-Meunier, B, Briggs, T A, Beresford, M W & Crow, Y J 2020, ' Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts ', The Lancet Rheumatology . https://doi.org/10.1016/S2665-9913(19)30142-0
Summary Background Systemic lupus erythematosus (SLE) is a rare immunological disorder and genetic factors are considered important in its causation. Monogenic lupus has been associated with around 30 genotypes in humans and 60 in mice, while genome-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a7737ea37ac192ff9add609775a9374
https://hal.archives-ouvertes.fr/hal-03065973
https://hal.archives-ouvertes.fr/hal-03065973
Autor:
Jagadeesh Bayry, Caroline Galeotti
Publikováno v:
Nature Reviews Rheumatology
Nature Reviews Rheumatology, Nature Publishing Group, 2020, ⟨10.1038/s41584-020-0448-7⟩
Nature Reviews. Rheumatology
Nature Reviews Rheumatology, Nature Publishing Group, 2020, ⟨10.1038/s41584-020-0448-7⟩
Nature Reviews. Rheumatology
International audience; Emerging reports show that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection precedes the appearance of various autoimmune and autoinflammatory diseases, including paediatric inflammatory multisystemic syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36cb878c91f3e481d6d495f1437c42db
https://www.hal.inserm.fr/inserm-02887529/document
https://www.hal.inserm.fr/inserm-02887529/document
Autor:
Guillaume Sarrabay, Véronique Hentgen, Caroline Galeotti, David Saadoun, Linda Rossi-Semerano, Sophie Georgin-Laviallec, Léa Savey, Isabelle Touitou, Isabelle Koné-Paut
Publikováno v:
Joint Bone Spine
Joint Bone Spine, Elsevier Masson, 2019, 86 (5), pp.554-561. ⟨10.1016/j.jbspin.2018.11.003⟩
Joint Bone Spine, Elsevier Masson, 2019, 86 (5), pp.554-561. ⟨10.1016/j.jbspin.2018.11.003⟩
International audience; The spectrum of factors known to mediate autoinflammation has broadened recently to include not only interleukin-1 (IL-1) and interferon, but also abnormalities that impair NF-κB pathway negative regulation. The NF-κB pathwa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28080c4c2a04845174bb85d0cc1eae65
https://hal.archives-ouvertes.fr/hal-02372848
https://hal.archives-ouvertes.fr/hal-02372848
Autor:
Guillaume Sarrabay, Isabelle Touitou, Sophie Georgin-Lavialle, Caroline Galeotti, Isabelle Koné-Paut
Publikováno v:
La Revue De Médecine Interne
La Revue De Médecine Interne, Elsevier, 2018, 39 (4), pp.265-270. ⟨10.1016/j.revmed.2016.08.019⟩
La Revue De Médecine Interne, Elsevier, 2018, 39 (4), pp.265-270. ⟨10.1016/j.revmed.2016.08.019⟩
Mevalonate kinase deficiency is a rare, autosomal recessive, auto-inflammatory disease. This results from mutations in the gene MVK coding for the enzyme mevalonate kinase. This enzyme is involved in cholesterol and isoprenoids synthesis. Depending p
Autor:
Alexandre Belot, Charlotte Samaille, Anne Pagnier, Hugues Flodrops, Frédéric Rieux-Laucat, François Maurier, Tiphanie Ginhoux, Olivia Weill, Ulrich Meinzer, Stéphane Burtey, Aurélia Lanteri, Irène Lemelle, Maryam Piram, Behrouz Kassai, Héloïse Reumaux, Christophe Malcus, Eric Hachulla, Caroline Galeotti, Bruno Ranchin, Isabelle Rouvet, Sandrine Morell Dubois, Pauline Soulas-Sprauel, Nicole Fabien, Aurélia Carbasse, Isabelle Koné-Paut, Brigitte Bader-Meunier, V. Despert, Stéphane Decramer, Hélène Lefebvre, Yanick J. Crow
Publikováno v:
Revue du Rhumatisme. 84:221-225
Resume Objectif L’etude des formes pediatriques de lupus erythemateux systemique (LES) a permis recemment l’identification de formes monogeniques de LES. L’objectif principal de cette etude est de decrire les premiers patients inclus dans l’e
Autor:
Guilaine Boursier, Linda Rossi-Semerano, Isabelle Touitou, Hentgen, Caroline Galeotti, Sophie Georgin-Lavialle, Eric Hachulla, Guillaume Sarrabay, Alexandre Belot, Cécile Rittore
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine; Volume 8; Issue 10; Pages: 1729
Journal of Clinical Medicine, Vol 8, Iss 10, p 1729 (2019)
Journal of Clinical Medicine; Volume 8; Issue 10; Pages: 1729
Journal of Clinical Medicine, Vol 8, Iss 10, p 1729 (2019)
Monogenic autoinflammatory diseases (AIDs) are caused by variants in genes that regulate innate immunity. The current diagnostic performance of targeted next-generation sequencing (NGS) for AIDs is low. We assessed whether pre-analytic advice from ex