Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Caroline Galeotti"'
Publikováno v:
Frontiers in Medicine. 9
Autoimmune disorders have been well characterized over the years and many pathways—but not all of them–have been found to explain their pathophysiology. Autoinflammatory disorders, on the other hand, are still hiding most of their molecular and c
Autor:
Caroline Galeotti, Jérémie Delaleu, Claire Ballot-Schmit, Charlotte Borocco, Eric Jeziorski, Eric Oksenhendler, Isabelle Koné-Paut, Yves Perel, Sarah Jannier, Nathalie Aladjidi, Vannina Giacobbi-Milet, Oanez Ackermann, François Maurier, Christophe Piguet
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2020, 15 (1), pp.95. ⟨10.1186/s13023-020-1345-5⟩
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2020, 15 (1), pp.95. ⟨10.1186/s13023-020-1345-5⟩
Background Castleman disease (CD) is a rare non-malignant lymphoproliferation of undetermined origin. Two major disease phenotypes can be distinguished: unicentric CD (UCD) and multicentric CD (MCD). Diagnosis confirmation is based on histopathologic
Autor:
Fanny Bajolle, Mathie Lorrot, Arnaud Wiedemann, Marion Grimaud, Slimane Allali, Fouad Madhi, Mehdi Oualha, Ulrich Meinzer, Noémie Lachaume, Corinne Levy, Jeanne Bordet, Pierre-Louis Leger, Alexandre Belot, Caroline Ovaert, Etienne Javouhey, Julie Toubiana, Marie-Laure Girardin, Alexis Mandelcwajg, Robert Cohen, Blandine Biot, François Angoulvant, Denise Antona, Caroline Galeotti, David D. Yang, Ana-Maria Paulet, Naim Ouldali, Jean-Emmanuel Kahn, Michael Levy, Caroline Claude, Morgane Dumortier, Lucas Percheron, Constance Beyler
Publikováno v:
JAMA
Journal of the American Medical Association
Journal of the American Medical Association, 2021, 325 (9), pp.855-864. ⟨10.1001/jama.2021.0694⟩
Journal of the American Medical Association, American Medical Association (AMA), 2021, 325 (9), pp.855-864. ⟨10.1001/jama.2021.0694⟩
Journal of the American Medical Association
Journal of the American Medical Association, 2021, 325 (9), pp.855-864. ⟨10.1001/jama.2021.0694⟩
Journal of the American Medical Association, American Medical Association (AMA), 2021, 325 (9), pp.855-864. ⟨10.1001/jama.2021.0694⟩
International audience; Importance: Multisystem inflammatory syndrome in children (MIS-C) is the most severe pediatric disease associated with severe acute respiratory syndrome coronavirus 2 infection, potentially life-threatening, but the optimal th
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
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 2, p 510 (2020)
International Journal of Molecular Sciences, 2020, 21 (2), pp.510. ⟨10.3390/ijms21020510⟩
International Journal of Molecular Sciences, MDPI, 2020, 21 (2), pp.510. ⟨10.3390/ijms21020510⟩
Volume 21
Issue 2
International Journal of Molecular Sciences, Vol 21, Iss 2, p 510 (2020)
International Journal of Molecular Sciences, 2020, 21 (2), pp.510. ⟨10.3390/ijms21020510⟩
International Journal of Molecular Sciences, MDPI, 2020, 21 (2), pp.510. ⟨10.3390/ijms21020510⟩
Volume 21
Issue 2
International audience; Basophils are rare granulocytes and dysregulated functions of these cells are associated with several atopic and non-atopic allergic diseases of skin, respiratory system and gastrointestinal tract. Both cytokines and immunoglo
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
Autor:
Emmanuel Stephen-Victor, Meenu Sharma, Caroline Galeotti, Patrick Bruneval, Anupama Karnam, Srini V. Kaveri, Mrinmoy Das, Mohan S. Maddur, Jagadeesh Bayry
Publikováno v:
Science Immunology
Science Immunology, American Association for the Advancement of Science, 2018, 3 (23), pp.eaan0829. ⟨10.1126/sciimmunol.aan0829⟩
Science Immunology, American Association for the Advancement of Science, 2018, 3 (23), pp.eaan0829. ⟨10.1126/sciimmunol.aan0829⟩
International audience; Basophils are a rare granulocyte population that has been associated with allergic and inflammatory responses. It is essential to understand the regulatory mechanisms by which basophils are kept in check, considering the impac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf1fdb94c49d49cec83502fbd18e4bce
https://hal.sorbonne-universite.fr/hal-01817714/document
https://hal.sorbonne-universite.fr/hal-01817714/document
Publikováno v:
International Immunology
International Immunology, 2017, 29 (11), pp.491-498. ⟨10.1093/intimm/dxx039⟩
International Immunology, Oxford University Press (OUP), 2017, 29 (11), pp.491-498. ⟨10.1093/intimm/dxx039⟩
International Immunology, 2017, 29 (11), pp.491-498. ⟨10.1093/intimm/dxx039⟩
International Immunology, Oxford University Press (OUP), 2017, 29 (11), pp.491-498. ⟨10.1093/intimm/dxx039⟩
Intravenous immunoglobulin (IVIG) is a pooled preparation of normal IgG obtained from several thousand healthy donors. It is widely used in the immunotherapy of a large number of autoimmune and inflammatory diseases. The mechanisms of action of IVIG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dcde79b1905500f4c3bd961c73e9229
https://hal.sorbonne-universite.fr/hal-01723555/document
https://hal.sorbonne-universite.fr/hal-01723555/document
Autor:
Bruno Fautrel, Isabelle Koné-Paut, Isabelle Touitou, Luca Semerano, Eric Hachulla, Linda Rossi-Semerano, Caroline Galeotti, Daniel Wendling
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2015, 10, pp.19. ⟨10.1186/s13023-015-0228-7⟩
Orphanet Journal of Rare Diseases, 2015, 10, pp.19. ⟨10.1186/s13023-015-0228-7⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2015, 10, pp.19. ⟨10.1186/s13023-015-0228-7⟩
Orphanet Journal of Rare Diseases, 2015, 10, pp.19. ⟨10.1186/s13023-015-0228-7⟩
Background Despite their limited licensed indications, anti–interleukin-1 (anti–IL-1) agents are often used in clinical practice for an increasing number of auto-inflammatory diseases. We conducted a national cross-sectional observational study f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6a0076e0b79b81653ef1c6df37c0c59
https://hal.sorbonne-universite.fr/hal-01275718/document
https://hal.sorbonne-universite.fr/hal-01275718/document
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 103(12)
Aim The most common manifestation of sickle cell disease (SCD) is painful vaso-occlusive episodes (PVOE), and inappropriate treatment leads to unnecessary suffering and potentially fatal complications. This study describes how French paediatric emerg