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Reference Centre of Sickle Cell Disease,
Hematology Unit,
Reference Centre of Sickle Cell Disease, Hematology Unit
Malika Benkerrou has not added Biography.
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Hydroxyurea corrects the dysregulated L-selectin expression and increased H(2)O(2) production of polymorphonuclear neutrophils from patients with sickle cell anemia.
Blood Apr, 2002 | Pubmed ID: 11895759
Decreased plasma endothelin-1 levels in children with sickle cell disease treated with hydroxyurea.
Haematologica Mar, 2005 | Pubmed ID: 15749673
Autoimmune liver disease in three children with sickle cell disease.
Journal of pediatric gastroenterology and nutrition Jan, 2006 | Pubmed ID: 16385263
Steroid treatment in children with sickle-cell disease.
Haematologica Mar, 2007 | Pubmed ID: 17339198
A primary immunodeficiency characterized by defective immunoglobulin class switch recombination and impaired DNA repair.
The Journal of experimental medicine May, 2007 | Pubmed ID: 17485519
[Hamartoma of the spleen (splenoma) in a child with sickle cell anemia].
Annales de pathologie Feb, 2007 | Pubmed ID: 17568356
Increased cerebral blood flow velocity in children with sickle cell disease: adenotonsillectomy or transfusion regimens?
Pediatrics Jul, 2007 | Pubmed ID: 17606584
Immunogenicity and safety of a pneumococcal conjugate 7-valent vaccine in infants with sickle cell disease.
The Pediatric infectious disease journal Dec, 2007 | Pubmed ID: 18043446
Modulation of erythroid adhesion receptor expression by hydroxyurea in children with sickle cell disease.
Haematologica Apr, 2008 | Pubmed ID: 18322255
Generalized periodontitis associated with Chédiak-Higashi syndrome.
Journal of periodontology Jul, 2008 | Pubmed ID: 18597610
Effect of transfusion therapy on cerebral vasculopathy in children with sickle-cell anemia.
Haematologica Jan, 2009 | Pubmed ID: 19059938
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.
American journal of hematology Jun, 2009 | Pubmed ID: 19425063
Pediatric acute pancreatitis related to tigecycline.
The Pediatric infectious disease journal Sep, 2010 | Pubmed ID: 20720475
Pathophysiology of sickle cell disease is mirrored by the red blood cell metabolome.
Blood Feb, 2011 | Pubmed ID: 21135259
Acute splenic sequestration crisis in sickle cell disease: cohort study of 190 paediatric patients.
British journal of haematology Mar, 2012 | Pubmed ID: 22224796
Fetal hemoglobin and hydroxycarbamide moduate both plasma concentration and cellular origin of circulating microparticles in sickle cell anemia children.
Haematologica Jun, 2013 | Pubmed ID: 23403312
Morbidity among child travellers with sickle-cell disease visiting tropical areas: an observational study in a French tertiary care centre.
Archives of disease in childhood Jul, 2013 | Pubmed ID: 23661574
Hematogenous Osteoarticular Infections of the Hand and the Wrist in Children With Sickle Cell Anemia: Preliminary Report.
Journal of pediatric orthopedics Jun, 2013 | Pubmed ID: 23812139
Impact of glucose-6-phosphate dehydrogenase deficiency on sickle cell anaemia expression in infancy and early childhood: a prospective study.
British journal of haematology Dec, 2013 | Pubmed ID: 24117340
Extracranial carotid arteriopathy in stroke-free children with sickle cell anemia: detection by submandibular Doppler sonography.
Pediatric radiology May, 2014 | Pubmed ID: 24595876
[Indications for allogeneic hematopoietic stem cell transplantion in sickle cell disease].
La Revue du praticien Oct, 2014 | Pubmed ID: 25510143
Clinical and haematological risk factors for cerebral macrovasculopathy in a sickle cell disease newborn cohort: a prospective study.
British journal of haematology Mar, 2016 | Pubmed ID: 26728571
Comparison of automated erythrocytapheresis versus manual exchange transfusion to treat cerebral macrovasculopathy in sickle cell anemia.
Transfusion May, 2016 | Pubmed ID: 27021622
Improvement of medical care in a cohort of newborns with sickle-cell disease in North Paris: impact of national guidelines.
British journal of haematology Jun, 2016 | Pubmed ID: 27062606
Robert Debré Hospital, AP-HP
Bérengère Koehl1,
Florence Missud1,
Laurent Holvoet1,
Ghislaine Ithier1,
Oliver Sakalian-Black2,
Zinedine Haouari1,
Emmanuelle Lesprit3,
André Baruchel4,
Malika Benkerrou1
1Reference Centre of Sickle Cell Disease, Hematology Unit, Robert Debré Hospital, AP-HP,
2School of Pharmacy, Université Paris Descartes,
3Etablissement Français du Sang, Robert Debré Hospital, AP-HP,
4Hematology Unit,, Robert Debré Hospital, AP-HP, Univsité Paris Diderot
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