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Break down the barriers of auto‐inflammation: How to deal with a monogenic auto‐inflammatory disease and immuno‐haematological features in 2022?

Immunology, 2023-01, Vol.168 (1), p.1-17

2023

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Azacitidine for patients with Vacuoles, E1 Enzyme, X‐linked, Autoinflammatory, Somatic syndrome (VEXAS) and myelodysplastic syndrome: data from the French VEXAS registry

British journal of haematology, 2022-02, Vol.196 (4), p.969-974

2022

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Waldenstrom macroglobulinaemia with AA amyloidosis reveals a B‐cell‐restricted NLRP2 variant

British journal of haematology, 2024-05, Vol.204 (5), p.2117-2120

2024

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Not Jessner‐Kanof But Cutaneous Lymphoid Hyperplasia Induced by Etanercept: Comment on the Clinical Images Report by Abbad et al

Arthritis & rheumatology (Hoboken, N.J.), 2018-09, Vol.70 (9), p.1530-1530

2018

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Commentary to “A 44‐year‐old female with familial Mediterranean fever, cardiomyopathy and end stage renal disease” by Magaki et al

Brain pathology (Zurich, Switzerland), 2019-03, Vol.29 (2), p.311-311

2019

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The “Mast Cell and Basophil Club” of the French Society for Immunology

European journal of immunology, 2020-10, Vol.50 (10), p.1430-1431

2020

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The association of psychiatric comorbidities with emergency visits and hospitalisations in adult sickle‐cell patients: a cohort study

British journal of haematology, 2020-04, Vol.189 (1), p.e21-e23

2020

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Chronic hepatic involvement in the clinical spectrum of A20 haploinsufficiency

Liver international, 2021-08, Vol.41 (8), p.1894-1900

2021

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Non‐amyloid liver involvement in familial Mediterranean fever: A systematic literature review

Liver international, 2020-06, Vol.40 (6), p.1269-1277

2020

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Plasma histamine elevation in a large cohort of sickle cell disease patients

British journal of haematology, 2019-07, Vol.186 (1), p.125-129

2019

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Helicobacter pylori in familial mediterranean fever: A series of 120 patients from literature and from france

Helicobacter (Cambridge, Mass.), 2021-04, Vol.26 (2), p.e12789-n/a

2021

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Provisional diagnostic criteria for systemic inflammatory trunk recurrent acute macular eruption diagnosis

Journal of the European Academy of Dermatology and Venereology, 2024-05

2024

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In familial Mediterranean fever, soluble TREM-1 plasma level is higher in case of amyloidosis

Innate immunity (London, England), 2019-11, Vol.25 (8), p.487-490

2019

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Response letter to "Latent class analysis of 216 patients with adult-onset Still's disease" by Sugiyama et al

Arthritis research & therapy, 2022-12, Vol.24 (1), p.285-285, Article 285

2022

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Impact of human monocyte and macrophage polarization on NLR expression and NLRP3 inflammasome activation

PloS one, 2017-04, Vol.12 (4), p.e0175336-e0175336

2017

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The Use of Interleukine-1 Inhibitors in Familial Mediterranean Fever Patients: A Narrative Review

Frontiers in immunology, 2020-05, Vol.11, p.971

2020

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Response to Letter to the Editor

Innate Immunity, 2020-04, Vol.26 (3), p.232-233

2020

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VEXAS syndrome: still expanding the clinical phenotype

Rheumatology (Oxford, England), 2021-09, Vol.60 (9), p.e321-e323

2021

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Mast cell leukemia

Blood, 2013-02, Vol.121 (8), p.1285-1295

2013

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Mast cell leukemia: identification of a new c-Kit mutation, dup(501-502), and response to masitinib, a c-Kit tyrosine kinase inhibitor

European journal of haematology, 2012-07, Vol.89 (1), p.47-52

2012

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Commentary: 'Case Report: A Rare Case of Elderly-Onset Adult Onset Still's Disease in a Patient With Systemic Lupus Erythematous'

Frontiers in immunology, 2022-04, Vol.13, p.876477

2022

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Canakinumab treatment real world evidence in 3 monogenic periodic fever syndromes in 2009-2022: an interim analysis using the French JIR cohort database

Arthritis research & therapy, 2024-04, Vol.26 (1), p.80-80, Article 80

2024

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Association of Vasculitis and Familial Mediterranean Fever

Frontiers in immunology, 2019-04, Vol.10, p.763-763

2019

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NLRP3-associated autoinflammatory diseases: Phenotypic and molecular characteristics of germline versus somatic mutations

Journal of allergy and clinical immunology, 2020-04, Vol.145 (4), p.1254-1261

2020

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Looking beyond VEXAS: Coexistence of undifferentiated systemic autoinflammatory disease and myelodysplastic syndrome

Seminars in hematology, 2021-10, Vol.58 (4), p.247-253

2021

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Break down the barriers of auto‐inflammation: How to deal with a monogenic auto‐inflammatory disease and immuno‐haematological features in 2022?

Azacitidine for patients with Vacuoles, E1 Enzyme, X‐linked, Autoinflammatory, Somatic syndrome (VEXAS) and myelodysplastic syndrome: data from the French VEXAS registry

Waldenstrom macroglobulinaemia with AA amyloidosis reveals a B‐cell‐restricted NLRP2 variant

Not Jessner‐Kanof But Cutaneous Lymphoid Hyperplasia Induced by Etanercept: Comment on the Clinical Images Report by Abbad et al

Commentary to “A 44‐year‐old female with familial Mediterranean fever, cardiomyopathy and end stage renal disease” by Magaki et al

The “Mast Cell and Basophil Club” of the French Society for Immunology

The association of psychiatric comorbidities with emergency visits and hospitalisations in adult sickle‐cell patients: a cohort study

Chronic hepatic involvement in the clinical spectrum of A20 haploinsufficiency

Non‐amyloid liver involvement in familial Mediterranean fever: A systematic literature review

Plasma histamine elevation in a large cohort of sickle cell disease patients

Helicobacter pylori in familial mediterranean fever: A series of 120 patients from literature and from france

Provisional diagnostic criteria for systemic inflammatory trunk recurrent acute macular eruption diagnosis

In familial Mediterranean fever, soluble TREM-1 plasma level is higher in case of amyloidosis

Response letter to "Latent class analysis of 216 patients with adult-onset Still's disease" by Sugiyama et al

Impact of human monocyte and macrophage polarization on NLR expression and NLRP3 inflammasome activation

The Use of Interleukine-1 Inhibitors in Familial Mediterranean Fever Patients: A Narrative Review

Response to Letter to the Editor

VEXAS syndrome: still expanding the clinical phenotype

Mast cell leukemia

Mast cell leukemia: identification of a new c-Kit mutation, dup(501-502), and response to masitinib, a c-Kit tyrosine kinase inhibitor

Commentary: 'Case Report: A Rare Case of Elderly-Onset Adult Onset Still's Disease in a Patient With Systemic Lupus Erythematous'

Canakinumab treatment real world evidence in 3 monogenic periodic fever syndromes in 2009-2022: an interim analysis using the French JIR cohort database

Association of Vasculitis and Familial Mediterranean Fever

NLRP3-associated autoinflammatory diseases: Phenotypic and molecular characteristics of germline versus somatic mutations

Looking beyond VEXAS: Coexistence of undifferentiated systemic autoinflammatory disease and myelodysplastic syndrome

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