Zobrazeno 1 - 10
of 218
pro vyhledávání: '"F. Gaches"'
Autor:
E. Bories, S. De Almeida, T. Porel, L. Alric, L. Astudillo, F. Gaches, M. Michaud, F. Catros, G. Prevot, L. Sailler, D. Adoue, O. Lairez, G. Pugnet
Publikováno v:
La Revue de Médecine Interne. 43:A81-A82
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfdba4d5ea9113e429e61cdb0dc04b3a
https://doi.org/10.1016/j.revmed.2022.03.261
https://doi.org/10.1016/j.revmed.2022.03.261
Autor:
S. De Almeida Chaves, B. Puissant, T. Porel, E. Bories, D. Adoue, L. Astudillo, L. Alric, A. Huart, M. Michaud, D. Ribes, G. Prevot, L. Sailler, F. Gaches, G. Pugnet
Publikováno v:
La Revue de Médecine Interne. 43:A76-A77
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e00a43bb519a40be38589e5bf84aa41a
https://doi.org/10.1016/j.revmed.2022.03.254
https://doi.org/10.1016/j.revmed.2022.03.254
Autor:
S. De Almeida Chaves, P. Benedicte, T. Porel, E. Bories, D. Adoue, L. Astudillo, L. Alric, A. Huart, M. Michaud, D. Ribes, G. Prevot, L. Sailler, F. Gaches, G. Pugnet
Publikováno v:
Annals of the Rheumatic Diseases. 81:1452.1-1452
BackgroundSystemic sclerosis (SSc) is reported to be a secondary cause of cryoglobulinemia as well as cryofibrinogenemia. However, prevalence, clinical implication and associated pronostic of cryoprecipitates in SSc are unknown.ObjectivesTo describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f76ebb3c375c152f4414caf2021cec3
https://doi.org/10.1136/annrheumdis-2022-eular.475
https://doi.org/10.1136/annrheumdis-2022-eular.475
Autor:
E. Bories, S. DE Almeida Chaves, T. Porel, L. Alric, L. Astudillo, F. Gaches, M. Michaud, F. Catros, G. Prevot, L. Sailler, D. Adoue, O. Lairez, G. Pugnet
Publikováno v:
Annals of the Rheumatic Diseases. 81:738.1-738
BackgroundThe prevalence of cardiac involvement in systemic sclerosis (SSc) varies in the literature between 3% and 44% and represents a leading cause of mortality in this disease. The incidence of severe cardiac involvement and the factors associate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0aae5b5310645ce95d340f1a06f377e
https://doi.org/10.1136/annrheumdis-2022-eular.2842
https://doi.org/10.1136/annrheumdis-2022-eular.2842
Autor:
M, Michaud, W, Mauhin, N, Belmatoug, N, Bedreddine, R, Garnotel, F, Catros, O, Lidove, F, Gaches
Publikováno v:
La Revue de medecine interne. 42(2)
Fabry disease is the second most frequent lysosomal storage disorder. It is a X-linked genetic disease secondary to alpha-galactosidase A enzyme deficiency. This is a progressive and systemic disease that affects both males and females. Classical sym
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::744ac102ccacc2f4ba37e515dfb93af7
https://pubmed.ncbi.nlm.nih.gov/33172708
https://pubmed.ncbi.nlm.nih.gov/33172708
Autor:
B. Granel, J. Sibilia, Luc Mouthon, T. Martin, E. Hachulla, P. Jego, A. Lescoat, Yannick Allanore, Patrick H. Carpentier, Arsène Mekinian, M.E. Truchetet, D. Farge, P. Senet, F. Gaches
Publikováno v:
Revue des Maladies Respiratoires Actualités. 12:53-54
Introduction La sclerodermie systemique (ScS) est une affection generalisee du tissu conjonctif, des arterioles et des micro-vaisseaux, caracterisee par la survenue de phenomenes de fibrose et d’obliteration vasculaire : – l’atteinte pulmonaire
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a94424b197f79d592e0373130fdf573
https://doi.org/10.1016/j.rmra.2019.11.092
https://doi.org/10.1016/j.rmra.2019.11.092
Autor:
A. Debard, S. Ancellin, Grégoire Prévot, M. Guille, Anne Hitzel, Grégory Pugnet, F. Catros, Olivier Lairez, F. Gaches, Martin Michaud
Publikováno v:
La Revue de Médecine Interne. 40:A48-A49
Introduction La pericardite est une pathologie frequente. Elle est responsable de 5 % des hospitalisations pour douleurs thoraciques. La tuberculose est la cause principale dans les pays ou cette infection est epidemique. Dans les pays industrialises
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df125378390aa0722ae3acc697fa1b21
https://doi.org/10.1016/j.revmed.2019.10.039
https://doi.org/10.1016/j.revmed.2019.10.039
Publikováno v:
La Revue de medecine interne. 41(3)
Mucopolysaccharidosis are lysosomal storage diseases, secondary to the accumulation of mucopolysaccharides. Type 1 mucopolysaccharidosis is the most common form and affects between 0.69 and 1.66 newborns per 100,000. The severity of mucopolysaccharid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e6378f45545c210f912f0251b761ecff
https://pubmed.ncbi.nlm.nih.gov/31959364
https://pubmed.ncbi.nlm.nih.gov/31959364
Publikováno v:
La Revue de medecine interne. 40(8)
Classification criteria for systemic sclerosis evolved over the last three decades, allowing an earlier classification. In the late 2000s, the EULAR Scleroderma Trials and Research Group validated very early and early systemic sclerosis criteria. Ray
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1508ca4279ef751b409656a0640f0bdd
https://pubmed.ncbi.nlm.nih.gov/30981561
https://pubmed.ncbi.nlm.nih.gov/30981561
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