Search Results - "Haroche, J."

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  1. 1

    Drug‐induced sarcoidosis: an overview of the WHO pharmacovigilance database by Cohen Aubart, F., Lhote, R., Amoura, A., Valeyre, D., Haroche, J., Amoura, Z., Lebrun‐Vignes, B.

    Published in Journal of internal medicine (01-09-2020)
    “…Background There is a documented association between drug exposure and sarcoidosis‐like reactions. In this study, we used the largest pharmacovigilance…”
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    Journal Article
  2. 2

    Cutaneous manifestations of paediatric Erdheim–Chester disease, a histiocytosis of the ‘L’ group by Chasset, F., Haroche, J.

    Published in British journal of dermatology (1951) (01-01-2018)
    “…Linked Article: Su et al. Br J Dermatol 2018; 178:261–264…”
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    The cerebrospinal fluid CD4/CD8 ratio and interleukin‐6 and ‐10 levels in neurosarcoidosis: a multicenter, pragmatic, comparative study by Chazal, T., Costopoulos, M., Maillart, E., Fleury, C., Psimaras, D., Legendre, P., Pineton de Chambrun, M., Haroche, J., Lubetzki, C., Amoura, Z., Legarff‐Tavernier, M., Cohen Aubart, F.

    Published in European journal of neurology (01-10-2019)
    “…Background and purpose Neurosarcoidosis is a rare inflammatory disorder of unknown cause. The aim of this study was to evaluate the value of T/B lymphocyte…”
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  4. 4

    Endocrine Manifestations in a Monocentric Cohort of 64 Patients With Erdheim-Chester Disease by Courtillot, C, Laugier Robiolle, S, Cohen Aubart, F, Leban, M, Renard-Penna, R, Drier, A, Charlotte, F, Amoura, Z, Touraine, P, Haroche, J

    “…Context: Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis, characterized by infiltration of foamy histiocytes in multiple organs…”
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    Pulmonary fibrosis associated with ANCA-positive vasculitides. Retrospective study of 12 cases and review of the literature by Hervier, B, Pagnoux, C, Agard, C, Haroche, J, Amoura, Z, Guillevin, L, Hamidou, M A

    Published in Annals of the rheumatic diseases (01-03-2009)
    “…To describe the clinical presentation of the association between pulmonary fibrosis (PF) and systemic vasculitis related to antineutrophil cytoplasmic…”
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  7. 7

    MRI features of intra-axial histiocytic brain mass lesions by Luna, L.P., Drier, A., Aygun, N., Mokhtari, K., Hoang-Xuan, K., Galanaud, D., Donadieu, J., Dormont, D., Haroche, J., Martin-Duverneuil, N.

    Published in Clinical radiology (01-02-2021)
    “…To describe MRI features, including diffusion-weighted imaging (DWI), magnetic resonance spectroscopy (MRS), and perfusion-weighted imaging (PWI), of…”
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    Systemic lupus erythematosus associated with ANCA-associated vasculitis: an overlapping syndrome? by Hervier, B., Hamidou, M., Haroche, J., Durant, C., Mathian, A., Amoura, Z.

    Published in Rheumatology international (01-10-2012)
    “…Systemic lupus erythematosus (SLE) and small-sized vessel vasculitis are usually two distinguishable autoimmune diseases. However, a vasculitis may be found in…”
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    Rosai-Dorfman disease: Diagnosis and therapeutic challenges by Cohen Aubart, F, Haroche, J, Emile, J-F, Charlotte, F, Barete, S, Schleinitz, N, Donadieu, J, Amoura, Z

    Published in La revue de medecine interne (01-08-2018)
    “…Rosai-Dorfman disease (RDD) was first described by the French pathologist Paul Destombes in 1965. It frequently affects children or young adults and is…”
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    Posterior reversible encephalopathy syndrome during systemic lupus erythematosus: four new cases and review of the literature by Leroux, G., Sellam, J., Costedoat-Chalumeau, N., Le Thi Huong, D., Combes, A., Tieulié, N., Haroche, J., Amoura, Z., Nieszkowska, A., Chastre, J., Dormont, D., Piette, J-C.

    Published in Lupus (01-02-2008)
    “…Posterior reversible encephalopathy syndrome (PRES) associates various neurological manifestations (headaches, seizures, altered mental status, cortical…”
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    Use of targeting therapy in Erdheim-Chester disease: A case report with neurologic involvement by Berthe, P, Rouzic, N, Daelman, L, Jacobzone, C, Espitia, A, Cohen-Aubart, F, Haroche, J, Émile, J-F, Lorleac'h, A

    Published in La revue de medecine interne (01-06-2020)
    “…Erdheim-Chester disease (ECD) is a rare multisystemic disease characterised by an infiltration of various organs by CD68 CD1a histiocytes. The clinical and…”
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    Langerhans cell histiocytosis and Erdheim-Chester disease, a continuity? by Parreau, S, Haroche, J, Pommepuy, I, Emile, J F, Bourras, J C, Archambeaud, F

    Published in La revue de medecine interne (01-07-2017)
    “…Erdheim-Chester disease and langerhans cell histiocytosis are two rare diseases separate on clinical, radiological and histological aspects. However, several…”
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    Neurosarcoidosis: Diagnosis and therapeutic issues by Cohen Aubart, F, Galanaud, D, Haroche, J, Psimaras, D, Mathian, A, Hié, M, Le-Thi Huong Boutin, D, Charlotte, F, Maillart, E, Maisonobe, T, Amoura, Z

    Published in La revue de medecine interne (01-06-2017)
    “…Neurological localizations of sarcoidosis are heterogeneous and may affect virtually every part of the central or peripheral nervous system. They are often the…”
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    Sarcoidosis flare after autologous stem cell transplantation: An immune paradox? by Marchal, A, Charlotte, F, Maksud, P, Haroche, J, Lifferman, F, Miyara, M, Choquet, S, Amoura, Z, Cohen Aubart, F

    Published in La revue de medecine interne (01-09-2017)
    “…Sarcoidosis is a systemic granulomatous disorder of unknown cause. Apparition or flare of previously diagnosed sarcoidosis following hematopoietic stem cell…”
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    Cardiac sarcoidosis: Diagnosis and therapeutic challenges by Cohen Aubart, F, Nunes, H, Mathian, A, Haroche, J, Hié, M, Le-Thi Huong Boutin, D, Cluzel, P, Soussan, M, Waintraub, X, Fouret, P, Valeyre, D, Amoura, Z

    Published in La revue de medecine interne (01-01-2017)
    “…Sarcoidosis is a granulomatous disorder of unknown cause characterized by non-caseating granuloma in young adults. Cardiac involvement is rare and range from 2…”
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    Journal Article