Search Results - "Jego, P."

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  1. 1

    Survival and prognosis factors in systemic sclerosis: data of a French multicenter cohort, systematic review, and meta-analysis of the literature by Pokeerbux, M R, Giovannelli, J, Dauchet, L, Mouthon, L, Agard, C, Lega, J C, Allanore, Y, Jego, P, Bienvenu, B, Berthier, S, Mekinian, A, Hachulla, E, Launay, D

    Published in Arthritis research & therapy (03-04-2019)
    “…Data on survival and prognosis factors in incident cohorts are scarce in systemic sclerosis (SStc). To describe survival, standardized mortality ratio (SMR),…”
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    Combined pulmonary fibrosis and emphysema in systemic sclerosis: A syndrome associated with heavy morbidity and mortality by Champtiaux, N., Cottin, V., Chassagnon, G., Chaigne, B., Valeyre, D., Nunes, H., Hachulla, E., Launay, D., Crestani, B., Cazalets, C., Jego, P., Bussone, G., Bérezné, A., Guillevin, L., Revel, M.P., Cordier, J.F., Mouthon, L.

    Published in Seminars in arthritis and rheumatism (01-08-2019)
    “…The syndrome of combined pulmonary fibrosis and emphysema (CPFE) primarily due to tobacco smoking has been reported in connective tissue disease, but little is…”
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    Uncertainty management and medical skills: A clinical and educational reflexion by Belhomme, N, Jego, P, Pottier, P

    Published in La revue de medecine interne (01-06-2019)
    “…Uncertainty arises when information is not sufficient to predict the prognosis or the outcome following an intervention. It is omnipresent in medical daily…”
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    Diagnostic value of 18-F fluorodeoxyglucose PET/CT and bone scan in Schnitzler syndrome by Alix, L., Néel, A., Cador, B., Smail, A., Serratrice, J., Closs-Prophette, F., Jego, P., Devillers, A., Decaux, O.

    Published in Autoimmunity (Chur, Switzerland) (17-11-2019)
    “…Introduction: Schnitzler syndrome is an auto-inflammatory disease defined by chronic urticarial eruption and monoclonal gammopathy. 18 F fluorodeoxyglucose…”
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    Cessation of oral anticoagulants in antiphospholipid syndrome by Comarmond, C, Jego, P, Veyssier-Belot, C, Marie, I, Mekinian, A, Elmaleh-Sachs, A, Leroux, G, Saadoun, D, Oziol, E, Fraisse, T, Hyvernat, H, Thiercein-Legrand, M-F, Sarrot-Reynauld, F, Ferreira-Maldent, N, de Menthon, M, Goujard, C, Khau, D, Nguen, Y, Monnier, S, Michon, A, Castel, B, Decaux, O, Piette, J-C, Cacoub, P

    Published in Lupus (01-10-2017)
    “…Objective To study the outcome of patients with antiphospholipid syndrome (APS) after oral anticoagulant treatment cessation. Methods We performed a…”
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    Drug‐induced granulomatosis: is dupilumab the new kid on the block? by Belhomme, N., Gaignon, T., Jouneau, S., Misery, L., Abasq‐Thomas, C., Cador, B., Lecureur, V., Cadiou, S., Ballerie, A., Polard, E., Mensi, S., Jego, P., Lescoat, A.

    “…Dupilumab is an IgG4 antibody directed toward IL-4 and IL-13, two major effectors of the Th2 immunity response. It was originally developed for severe and/or…”
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    Using Rituximab Plus Fludarabine and Cyclophosphamide as a Treatment for Refractory Mixed Cryoglobulinemia Associated With Lymphoma by Saadoun, D., Pineton de Chambrun, M., Hermine, O., Karras, A., Choquet, S., Jego, P., Decaux, O., Cacoub, P.

    Published in Arthritis care & research (2010) (01-04-2013)
    “…Objective Treatment of refractory mixed cryoglobulinemia (MC) with severe organ involvement remains challenging. Fludarabine, cyclophosphamide, and rituximab…”
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    Libman-Sacks endocarditis under apixaban in a patient with a high-risk profile venous antiphospholipid syndrome by Allain, J-S, Paven, E, Henriot, B, Belhomme, N, Le Bot, A, Ballerie, A, Jego, P

    Published in La revue de medecine interne (01-03-2021)
    “…Libman-Sacks endocarditis is a rare complication of antiphospholipid syndrome. Anti-vitamin K therapy is the standard treatment, although valvular replacement…”
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    Aspirin: Indications and use during pregnancy by Belhomme, N, Doudnikoff, C, Polard, E, Henriot, B, Isly, H, Jego, P

    Published in La revue de medecine interne (01-12-2017)
    “…Aspirin (acetylsalicylic acid) has been used ever since the Antiquity for its painkilling and anti-inflammatory effects. Its antiplatelet properties have then…”
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    Illnesses unrelated to systemic sclerosis (IUSS) diagnosed throughout the patient's follow-up in a referral center: A cohort of 200 patients by Lepart, C, Ardois, S, Bismut, M, Ballerie, A, Cazalets, C, Coiffier, G, Jego, P, Belhomme, N, Lescoat, A

    Published in La revue de medecine interne (01-08-2020)
    “…Our work aimed to investigate the illnesses unrelated to systemic sclerosis (IUSS), diagnosed among patients with systemic sclerosis (SSc) throughout their…”
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    Intra-cardiac manifestation during adult-onset Still's disease's, a tricuspid vegetation as a rare expression of systemic disease by Quelven, Q, Cador, B, Poinot, M, Fletcher, E, Le Mouel, E, Jego, P

    Published in La revue de medecine interne (01-10-2018)
    “…Adult-onset Still's Disease is a rare multisystemic inflammatory disease characterized by fever, maculo-papular erythematous rash and arthralgia. Adult-onset…”
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    A microcytic sideroblastic anemia successfully treated with B6 vitamin by Allain, J-S, Belhomme, N, Henriot, B, Haas, M, Le Gall-Godard, M, Pastoret, C, Jego, P

    Published in La revue de medecine interne (01-07-2019)
    “…Sideroblastic anemia is a rare cause of microcytic anemia, which is characterized by ring sideroblasts on bone marrow aspirate. This anemia can be congenital…”
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    Use of a medical discharge sheet for medication reconciliation in an internal medicine department: Assessment of general practitioners' opinion by Alix, L, Dumay, M, Cador-Rousseau, B, Gilardi, H, Hue, B, Somme, D, Jego, P

    Published in La revue de medecine interne (01-06-2018)
    “…Medication reconciliation (MR) is a systematic and comprehensive review of all medication a patient is taking. In this study, a discharge medication sheet…”
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    Use of bosentan for digital ulcers related to systemic sclerosis: a real-life retrospective French study of 89 patients treated since specific approval by Agard, C, Carpentier, PH, Mouthon, L, Clerson, P, Gressin, V, Bérezné, A, Diot, E, Jego, P, Lok, C, Sparsa, A, Chatelus, E, Van Kien, A Khau, Quéré, I, Sibilia, J, Hachulla, E

    Published in Scandinavian journal of rheumatology (01-10-2014)
    “…Objectives: Ischaemic digital ulcers (DUs) are a common complication of systemic sclerosis (SSc). This study aimed to characterize patients with SSc and…”
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    Reliability and validity of a workbook for assessment of professional competencies of internal medicine residents by Bonnard, G, Cohen-Aubart, F, Steichen, O, Bourgarit, A, Abad, S, Ranque, B, Pouchot, J, Dossier, A, Espitia-Thibault, A, Jego, P, Granel, B, Launay, D, Rivière, E, Le Jeunne, C, Mouthon, L, Pottier, P

    Published in La revue de medecine interne (01-07-2019)
    “…Though several assessment tools for resident professional skills based on workplace direct observation have been validated, they remain scarcely used in…”
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    Hereditary thrombophilia testing and its therapeutic impact on venous thromboembolism disease: Results from a retrospective single-center study of 162 patients by Allain, J-S, Gueret, P, Le Gallou, T, Cazalets, C, Lescoat, A, Jego, P

    Published in La revue de medecine interne (01-10-2016)
    “…Venous thromboembolic disease is a multifactorial, frequently recurrent pathology, whose treatment is based on anticoagulation. As part of the etiological…”
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