High titers of autoantibodies in patients with sickle-cell disease
…, F Lionnet, I Hagege, F Boussa-Khettab… - The Journal of …, 2011 - jrheum.org
Objective. Frequency and titers of autoantibodies in patients with sickle-cell disease (SCD)
have been reported as relatively high. In a prospective study of 88 patients, we examined this …
have been reported as relatively high. In a prospective study of 88 patients, we examined this …
[HTML][HTML] Detection by flow cytometry of anti-DNA autoantibodies and circulating DNA immune complexes in lupus erythematosus
…, M Moumaris, F Boussa-Khettab… - Journal of Immunology …, 2019 - hindawi.com
A new method for the detection by flow cytometry of anti-double-stranded DNA antibodies
and of circulating immune complexes (IC) containing endogenous DNA (IC-eDNA) is …
and of circulating immune complexes (IC) containing endogenous DNA (IC-eDNA) is …
[CITATION][C] Evaluation de deux tests rapides, d'exclusion de thrombose veineuse profonde et/ou d'embolie pulmonaire
F Boussa-Khettab - 1997
[HTML][HTML] Systemic lupus erythematosus associated with sickle-cell disease: a case report and literature review
M Maamar, Z Tazi-Mezalek, H Harmouche… - Journal of medical case …, 2012 - Springer
Introduction The occurrence of systemic lupus erythematosus has been only rarely reported
in patients with sickle-cell disease. Case presentation We describe the case of a 23-year-old …
in patients with sickle-cell disease. Case presentation We describe the case of a 23-year-old …
[HTML][HTML] Coexistent sickle-cell anemia and autoimmune disease in eight children: pitfalls and challenges
V Li-Thiao-Te, F Uettwiller, P Quartier, F Lacaille… - Pediatric …, 2018 - Springer
Background Patients with sickle cell disease (SCD) present a defective activation of the
alternate complement pathway that increases the risk of infection and is thought to predispose to …
alternate complement pathway that increases the risk of infection and is thought to predispose to …
[HTML][HTML] A novel case report of sickle cell disease-associated immunoglobulin A nephropathy: the diagnostic value of erythrocyte dysmorphism evaluation
GEB Silva, AC Teixeira, JGG Vergna… - … Journal of Clinical …, 2014 - ncbi.nlm.nih.gov
Sickle cell disease is a severe disease with a genetic pattern; it may cause anemia, vaso-occlusive
phenomena, and multiorgan injury. It may damage any renal compartment, thereby …
phenomena, and multiorgan injury. It may damage any renal compartment, thereby …
[PDF][PDF] Systemic Lupus Erythematosus (SLE) with Sickle Cell Disease (SCD)-A Rare Case Series
A Nasreen, AK Sunil, M Shabeer, P Biswajit, SS Jagat… - researchgate.net
SLE and SCD are relatively common disorders especially in India and Africa but the combination
of connective tissue disease particularly SLE with SCD in a same individual appears to …
of connective tissue disease particularly SLE with SCD in a same individual appears to …
[PDF][PDF] Systemic lupus erythematosus associated with sickle-cell disease: a case report and
M Maamar, Z Tazi-Mezalek, H Harmouche… - 2012 - jmedicalcasereports.biomedcentral …
Introduction: The occurrence of systemic lupus erythematosus has been only rarely reported
in patients with sickle-cell disease. Case presentation: We describe the case of a 23-year-…
in patients with sickle-cell disease. Case presentation: We describe the case of a 23-year-…
Polymeric dexamethasone prodrugs attenuate lupus nephritis in MRL/lpr mice with reduced glucocorticoid toxicity
Due to their potent immunosuppressive and anti-inflammatory effects, glucocorticoids (GCs)
are the most widely used medications in treating lupus nephritis (LN). Long-term use of GCs, …
are the most widely used medications in treating lupus nephritis (LN). Long-term use of GCs, …
Sickle cell disease and systematic lupus erythematous association in a 14-year-old adolescent female: A case report
OY Safdar, STA Sindi, NWM Nazer… - Australasian …, 2019 - search.proquest.com
Background Sickle cell anaemia is caused by an autosomal recessive single gene defect in
the beta chain of haemoglobin (HbA), which results in production of sickle cell haemoglobin (…
the beta chain of haemoglobin (HbA), which results in production of sickle cell haemoglobin (…