Malika Benkerrou

Hydroxyurea corrects the dysregulated L-selectin expression and increased H(2)O(2) production of polymorphonuclear neutrophils from patients with sickle cell anemia.

Decreased plasma endothelin-1 levels in children with sickle cell disease treated with hydroxyurea.

Autoimmune liver disease in three children with sickle cell disease.

Steroid treatment in children with sickle-cell disease.

A primary immunodeficiency characterized by defective immunoglobulin class switch recombination and impaired DNA repair.

[Hamartoma of the spleen (splenoma) in a child with sickle cell anemia].

Increased cerebral blood flow velocity in children with sickle cell disease: adenotonsillectomy or transfusion regimens?

Immunogenicity and safety of a pneumococcal conjugate 7-valent vaccine in infants with sickle cell disease.

Modulation of erythroid adhesion receptor expression by hydroxyurea in children with sickle cell disease.

Generalized periodontitis associated with Chédiak-Higashi syndrome.

Effect of transfusion therapy on cerebral vasculopathy in children with sickle-cell anemia.

Effects of RANTES and MBL2 gene polymorphisms in sickle cell disease clinical outcomes: association of the g.In1.1T>C RANTES variant with protection against infections.

Pediatric acute pancreatitis related to tigecycline.

Pathophysiology of sickle cell disease is mirrored by the red blood cell metabolome.

Acute splenic sequestration crisis in sickle cell disease: cohort study of 190 paediatric patients.

Fetal hemoglobin and hydroxycarbamide moduate both plasma concentration and cellular origin of circulating microparticles in sickle cell anemia children.

Morbidity among child travellers with sickle-cell disease visiting tropical areas: an observational study in a French tertiary care centre.

Hematogenous Osteoarticular Infections of the Hand and the Wrist in Children With Sickle Cell Anemia: Preliminary Report.

Impact of glucose-6-phosphate dehydrogenase deficiency on sickle cell anaemia expression in infancy and early childhood: a prospective study.

Extracranial carotid arteriopathy in stroke-free children with sickle cell anemia: detection by submandibular Doppler sonography.

[Indications for allogeneic hematopoietic stem cell transplantion in sickle cell disease].

Clinical and haematological risk factors for cerebral macrovasculopathy in a sickle cell disease newborn cohort: a prospective study.

Comparison of automated erythrocytapheresis versus manual exchange transfusion to treat cerebral macrovasculopathy in sickle cell anemia.

Improvement of medical care in a cohort of newborns with sickle-cell disease in North Paris: impact of national guidelines.