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Relationships of HLA-B51 or B5 genotype with Behçet's disease clinical characteristics: systematic review and meta-analyses of observational studies

Rheumatology (Oxford, England), 2012-05, Vol.51 (5), p.887-900

2012

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Cold agglutinin disease as a new immune-related adverse event associated with anti-PD-L1s and its treatment with rituximab

European journal of cancer (1990), 2019-03, Vol.110, p.21-23

2019

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HLA–B51/B5 and the risk of Behçet's disease: A systematic review and meta‐analysis of case–control genetic association studies

Arthritis and rheumatism, 2009-10, Vol.61 (10), p.1287-1296

2009

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Autoimmune diseases in HIV-infected patients: 52 cases and literature review

Autoimmunity reviews, 2014-08, Vol.13 (8), p.850-857

2014

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Delayed-onset hypoxic cortical blindness: coming back from the abyss

Documenta ophthalmologica, 2022-04, Vol.144 (2), p.147-152

2022

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Rationale and efficacy of interleukin-1 targeting in Erdheim–Chester disease

Blood, 2010-11, Vol.116 (20), p.4070-4076

2010

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Histiocytose à cellules de Langerhans de l’adulte

La Presse médicale (1983), 2017-01, Vol.46 (1), p.55-69

2017

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Membranous nephropathy in primary antiphospholipid syndrome

Clinical kidney journal, 2024-02, Vol.17 (2), p.sfae017-sfae017

2024

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Psychiatric Symptoms and Cognitive Disorders in Behçet's Disease: A Single-Center, Cross-Sectional Study

Journal of clinical medicine, 2023-04, Vol.12 (9), p.3149

2023

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Clinical Spectrum, Quality of Life, BRAF Mutation Status and Treatment of Skin Involvement in Adult Langerhans Cell Histiocytosis

Acta dermato-venereologica, 2017-07, Vol.97 (7), p.838-842

2017

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Artérite à cellules géantes et maladie de Takayasu : aspects épidémiologiques, diagnostiques et thérapeutiques

La Presse médicale (1983), 2012-10, Vol.41 (10), p.955-965

2012

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Classification and classification criteria for vasculitis: achievements, limitations and prospects

Current opinion in rheumatology, 2015-01, Vol.27 (1), p.1-9

2015

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Management of adult patients with Langerhans cell histiocytosis: recommendations from an expert panel on behalf of Euro-Histio-Net

Orphanet journal of rare diseases, 2013-05, Vol.8 (1), p.72-72

2013

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Usual interstitial pneumonia in ANCA-associated vasculitis: A poor prognostic factor

Journal of autoimmunity, 2020-01, Vol.106, p.102338-102338, Article 102338

2020

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Hématome frontal révélant une vascularite primitive du système nerveux central

La Presse médicale (1983), 2009-05, Vol.38 (5), p.844-846

2009

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Treating polyarteritis nodosa: current state of the art

Clinical and experimental rheumatology, 2011-01, Vol.29 (1 Suppl 64), p.S110

2011

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Long‐term efficacy and safety of 2CdA (cladribine) in extra‐pulmonary adult‐onset Langerhans cell histiocytosis: analysis of 23 cases from the French Histiocytosis Group and systematic literature review

British journal of haematology, 2020-06, Vol.189 (5), p.869-878

2020

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Severe ulcerative gastrointestinal toxicity following ibrutinib therapy: two case studies

Leukemia & lymphoma, 2021-03, Vol.62 (4), p.984-987

2021

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Intraparenchymal hemorrhage disclosing a primary angiitis of the central nervous system

La Presse médicale (1983), 2009-05, Vol.38 (5), p.844

2009

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Rituximab as maintenance therapy for ANCA-associated vasculitides: pooled analysis and long-term outcome of 277 patients included in the MAINRITSAN trials

Annals of the rheumatic diseases, 2024-02, Vol.83 (2), p.233-241

2024

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Autoimmunity in sickle cell disease: Analysis of a large cohort of adult patients

American journal of hematology, 2023-11, Vol.98 (11), p.E315-E317

2023

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Neutrophilic Dermatoses in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis: A French Multicenter Study of 17 Cases and Literature Review

Medicine (Baltimore), 2016-03, Vol.95 (11), p.e2957-e2957

2016

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Inflammatory demyelinating polyneuropathies and lymphoma: clues to diagnosis and therapy

Leukemia & lymphoma, 2021-07, Vol.62 (8), p.2000-2004

2021

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Methemoglobinemia as a biomarker of dapsone-induced mania severity

Journal of affective disorders, 2019-07, Vol.254, p.122-123

2019

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Excessive interleukin‐15 transpresentation endows NKG2D+CD4+ T cells with innate‐like capacity to lyse vascular endothelium in granulomatosis with polyangiitis (Wegener's)

Arthritis & rheumatology (Hoboken, N.J.), 2011-07, Vol.63 (7), p.2116-2126

2011

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Relationships of HLA-B51 or B5 genotype with Behçet's disease clinical characteristics: systematic review and meta-analyses of observational studies

Cold agglutinin disease as a new immune-related adverse event associated with anti-PD-L1s and its treatment with rituximab

HLA–B51/B5 and the risk of Behçet's disease: A systematic review and meta‐analysis of case–control genetic association studies

Autoimmune diseases in HIV-infected patients: 52 cases and literature review

Delayed-onset hypoxic cortical blindness: coming back from the abyss

Rationale and efficacy of interleukin-1 targeting in Erdheim–Chester disease

Histiocytose à cellules de Langerhans de l’adulte

Membranous nephropathy in primary antiphospholipid syndrome

Psychiatric Symptoms and Cognitive Disorders in Behçet's Disease: A Single-Center, Cross-Sectional Study

Clinical Spectrum, Quality of Life, BRAF Mutation Status and Treatment of Skin Involvement in Adult Langerhans Cell Histiocytosis

Artérite à cellules géantes et maladie de Takayasu : aspects épidémiologiques, diagnostiques et thérapeutiques

Classification and classification criteria for vasculitis: achievements, limitations and prospects

Management of adult patients with Langerhans cell histiocytosis: recommendations from an expert panel on behalf of Euro-Histio-Net

Usual interstitial pneumonia in ANCA-associated vasculitis: A poor prognostic factor

Hématome frontal révélant une vascularite primitive du système nerveux central

Treating polyarteritis nodosa: current state of the art

Long‐term efficacy and safety of 2CdA (cladribine) in extra‐pulmonary adult‐onset Langerhans cell histiocytosis: analysis of 23 cases from the French Histiocytosis Group and systematic literature review

Severe ulcerative gastrointestinal toxicity following ibrutinib therapy: two case studies

Intraparenchymal hemorrhage disclosing a primary angiitis of the central nervous system

Rituximab as maintenance therapy for ANCA-associated vasculitides: pooled analysis and long-term outcome of 277 patients included in the MAINRITSAN trials

Autoimmunity in sickle cell disease: Analysis of a large cohort of adult patients

Neutrophilic Dermatoses in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis: A French Multicenter Study of 17 Cases and Literature Review

Inflammatory demyelinating polyneuropathies and lymphoma: clues to diagnosis and therapy

Methemoglobinemia as a biomarker of dapsone-induced mania severity

Excessive interleukin‐15 transpresentation endows NKG2D+CD4+ T cells with innate‐like capacity to lyse vascular endothelium in granulomatosis with polyangiitis (Wegener's)

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