Search Results - "Diot, E."

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  1. 1

    Comparison of long-term outcome between anti-Jo1- and anti-PL7/PL12 positive patients with antisynthetase syndrome by Marie, I, Josse, S, Decaux, O, Dominique, S, Diot, E, Landron, C, Roblot, P, Jouneau, S, Hatron, P.Y, Tiev, K.P, Vittecoq, O, Noel, D, Mouthon, L, Menard, J.-F, Jouen, F

    Published in Autoimmunity reviews (01-08-2012)
    “…Abstract The aims of the present study were to: compare the characteristics between antisynthetase syndrome (ASS) patients with anti-Jo1 antibody and those…”
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    Journal Article
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    Association of the TNFAIP3 rs5029939 variant with systemic sclerosis in the European Caucasian population by Dieudé, P, Guedj, M, Wipff, J, Ruiz, B, Riemekasten, G, Matucci-Cerinic, M, Melchers, I, Hachulla, E, Airo, P, Diot, E, Hunzelmann, N, Cabane, J, Mouthon, L, Cracowski, J L, Riccieri, V, Distler, J, Meyer, O, Kahan, A, Boileau, C, Allanore, Y

    Published in Annals of the rheumatic diseases (01-11-2010)
    “…TNFAIP3 encodes the ubiquitin-modifying enzyme, a key regulator of inflammatory signalling pathways. Convincing associations between TNFAIP3 variants and…”
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    Journal Article
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    Characteristics of patients with connective tissue disease-associated pulmonary arterial hypertension treated with prostanoids: A multicenter retrospective study by Genin, V, Horeau-Langlard, D, Diot, E, Gagnadoux, F, Lavigne, C, Fournet, M, Durant, C, Agard, C

    Published in La revue de medecine interne (01-12-2021)
    “…INTRODUCTIONPulmonary arterial hypertension (PAH) is a severe complication of connective tissue disease (CTD). Data on use of prostanoids in this particular…”
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    Giant cell arteritis-related aortitis with positive or negative temporal artery biopsy: a French multicentre study by Agard, C, Bonnard, G, Samson, M, de Moreuil, C, Lavigne, C, Jégo, P, Connault, J, Artifoni, M, Le Gallou, T, Landron, C, Roblot, P, Magnant, J, Belizna, C, Maillot, F, Diot, E, Néel, A, Hamidou, M, Espitia, O

    Published in Scandinavian journal of rheumatology (02-11-2019)
    “…Objective: To compare the clinical presentation and outcome of giant cell arteritis (GCA)-related aortitis according to the results of temporal artery biopsy…”
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    Long-term outcome of patients with polymyositis/ dermatomyositis and anti-PM-Scl antibody by Marie, I., Lahaxe, L., Benveniste, O., Delavigne, K., Adoue, D., Mouthon, L., Hachulla, E., Constans, J., Tiev, K., Diot, E., Levesque, H., Boyer, O., Jouen, F.

    Published in British journal of dermatology (1951) (01-02-2010)
    “…Summary Background  To date, no series has analysed long‐term outcome in patients with polymyositis/dermatomyositis (PM/DM) with anti‐PM‐Scl antibody…”
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    Journal Article
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    Clinical manifestations and outcome of anti-PL7 positive patients with antisynthetase syndrome by Marie, I, Josse, S, Decaux, O, Diot, E, Landron, C, Roblot, P, Jouneau, S, Hatron, P.Y, Hachulla, E, Vittecoq, O, Menard, J.-F, Jouen, F, Dominique, S

    Published in European journal of internal medicine (01-07-2013)
    “…Abstract Background The aims of the present study were to determine both clinical manifestations and outcome of anti-PL7 patients with antisynthetase syndrome…”
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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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    Organising pneumonia can be the inaugural manifestation in connective tissue diseases, including Sjogren's syndrome by Henriet, A C, Diot, E, Marchand-Adam, S, de Muret, A, Favelle, O, Crestani, B, Diot, P

    Published in European respiratory review (01-06-2010)
    “…Connective tissue diseases are known to be one of the causes of organising pneumonia (OP). However, this association is rare and signs of OP usually occur in…”
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    Pulmonary manifestations revealing Rosai-Dorfman disease by Goupil de Bouillé, J, de Muret, A, Diot, E, Dumont, P, Plantier, L, Diot, P, Marchand-Adam, Sylvain

    “…Rosai-Dorfman disease is a rare non-Langerhans cell histiocytosis, mainly involving cervical nodes. We present the case of a patient with a pulmonary form of…”
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