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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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Familial Mediterranean Fever in Heterozygotes: Are We Able to Accurately Diagnose the Disease in Very Young Children?

Arthritis & rheumatology (Hoboken, N.J.), 2013-06, Vol.65 (6), p.1654-1662

2013

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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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Lactate dehydrogenase in sickle cell disease

Clinica chimica acta, 2016-07, Vol.458, p.99-102

2016

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Nitrous oxide toxicity in adult patients with sickle cell disease

European journal of internal medicine, 2024-05

2024

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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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Concordance between CRP and SAA in familial Mediterranean fever during attack-free period: A study of 218 patients

Clinical biochemistry, 2017-03, Vol.50 (4-5), p.206-209

2017

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Hemoglobin sickle cell disease complications: a clinical study of 179 cases

Haematologica (Roma), 2012-08, Vol.97 (8), p.1136-1141

2012

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Dramatic beneficial effect of interleukin-1 inhibitor treatment in patients with familial Mediterranean fever complicated with amyloidosis and renal failure

Nephrology, dialysis, transplantation, 2012-05, Vol.27 (5), p.1898-1901

2012

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Association of hidradenitis suppurativa and familial Mediterranean fever: A case series of 6 patients

Joint, bone, spine : revue du rhumatisme, 2017-03, Vol.84 (2), p.159-162

2017

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How should we approach classification of autoinflammatory diseases?

Nature reviews. Rheumatology, 2013-10, Vol.9 (10), p.624

2013

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The risk of familial Mediterranean fever in MEFV heterozygotes: a statistical approach

PloS one, 2013-07, Vol.8 (7), p.e68431-e68431

2013

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Spondyloarthritis associated with familial Mediterranean fever: successful treatment with anakinra

Rheumatology, 2017-01, Vol.56 (1), p.167-169

2017

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Chronic myeloid leukaemia and sickle cell disease: could imatinib prevent vaso‐occlusive crisis?

British journal of haematology, 2011-10, Vol.155 (2), p.271-272

2011

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Renin‐angiotensin system blockade promotes a cardio‐renal protection in albuminuric homozygous sickle cell patients

British journal of haematology, 2017-12, Vol.179 (5), p.820-828

2017

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Cerebral fat embolism in hemoglobin SC disease

The American journal of medicine, 2017-05, Vol.130 (5), p.e187-e189

2017

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High lactate dehydrogenase levels at admission for painful vaso-occlusive crisis is associated with severe outcome in adult SCD patients

Clinical biochemistry, 2012-12, Vol.45 (18), p.1578-1582

2012

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Prevalence and correlates of metabolic acidosis among patients with homozygous sickle cell disease

Clinical journal of the American Society of Nephrology, 2014-04, Vol.9 (4), p.648-653

2014

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A preliminary score for the assessment of disease activity in hereditary recurrent fevers: results from the AIDAI (Auto-Inflammatory Diseases Activity Index) Consensus Conference

Annals of the rheumatic diseases, 2011-02, Vol.70 (2), p.309-314

2011

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Myositis in a patient with familial Mediterranean fever and spondyloarthritis successfully treated with anakinra

Joint, bone, spine : revue du rhumatisme, 2013-12, Vol.80 (6), p.645-649

2013

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Left atrial volume is not an index of left ventricular diastolic dysfunction in patients with sickle cell anaemia

Archives of cardiovascular diseases, 2015-03, Vol.108 (3), p.156-162

2015

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AA amyloidosis is an emerging cause of nephropathy in obese patients

European journal of internal medicine, 2017-04, Vol.39, p.e18-e20

2017

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Morpho-functional evaluation of lung aeration as a marker of sickle-cell acute chest syndrome severity in the ICU: a prospective cohort study

Annals of intensive care, 2019-09, Vol.9 (1), p.1-13, Article 109

2019

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Cystic fibrosis and AA amyloidosis: a survey in the French cystic fibrosis network

Amyloid, 2014-12, Vol.21 (4), p.231-237

2014

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Posterior reversible encephalopathy syndrome in an adult patient with sickle cell anemia

La Presse médicale (1983), 2013-03, Vol.42 (3), p.373-374

2013

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

Familial Mediterranean Fever in Heterozygotes: Are We Able to Accurately Diagnose the Disease in Very Young Children?

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

Lactate dehydrogenase in sickle cell disease

Nitrous oxide toxicity in adult patients with sickle cell disease

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

Concordance between CRP and SAA in familial Mediterranean fever during attack-free period: A study of 218 patients

Hemoglobin sickle cell disease complications: a clinical study of 179 cases

Dramatic beneficial effect of interleukin-1 inhibitor treatment in patients with familial Mediterranean fever complicated with amyloidosis and renal failure

Association of hidradenitis suppurativa and familial Mediterranean fever: A case series of 6 patients

How should we approach classification of autoinflammatory diseases?

The risk of familial Mediterranean fever in MEFV heterozygotes: a statistical approach

Spondyloarthritis associated with familial Mediterranean fever: successful treatment with anakinra

Chronic myeloid leukaemia and sickle cell disease: could imatinib prevent vaso‐occlusive crisis?

Renin‐angiotensin system blockade promotes a cardio‐renal protection in albuminuric homozygous sickle cell patients

Cerebral fat embolism in hemoglobin SC disease

High lactate dehydrogenase levels at admission for painful vaso-occlusive crisis is associated with severe outcome in adult SCD patients

Prevalence and correlates of metabolic acidosis among patients with homozygous sickle cell disease

A preliminary score for the assessment of disease activity in hereditary recurrent fevers: results from the AIDAI (Auto-Inflammatory Diseases Activity Index) Consensus Conference

Myositis in a patient with familial Mediterranean fever and spondyloarthritis successfully treated with anakinra

Left atrial volume is not an index of left ventricular diastolic dysfunction in patients with sickle cell anaemia

AA amyloidosis is an emerging cause of nephropathy in obese patients

Morpho-functional evaluation of lung aeration as a marker of sickle-cell acute chest syndrome severity in the ICU: a prospective cohort study

Cystic fibrosis and AA amyloidosis: a survey in the French cystic fibrosis network

Posterior reversible encephalopathy syndrome in an adult patient with sickle cell anemia

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