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You searched for: Author/Creator Renard, Cécile

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1. Alpha‐thalassaemia promotes frequent vaso‐occlusive crises in children with sickle cell anaemia through haemorheological changes. Issue 8 (18th January 2017)

3. G6PD deficiency and absence of α‐thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemia. (30th June 2015)

4. Haplo‐identical or mismatched unrelated donor hematopoietic cell transplantation for Fanconi anemia: Results from the Severe Aplastic Anemia Working Party of the EBMT. Issue 5 (4th March 2021)

5. Interest of the preventive and curative use of defibrotide on the occurrence and severity of sinusoidal obstruction syndrome after hematopoietic stem cell transplant in children. Issue 3 (31st May 2022)

7. Recurrent bacterial infections, but not fungal infections, characterise patients with ELANE‐related neutropenia: a French Severe Chronic Neutropenia Registry study. (2nd August 2021)

8. Recurrent bacterial infections, but not fungal infections, characterise patients with ELANE‐related neutropenia: a French Severe Chronic Neutropenia Registry study. (2nd August 2021)

9. UGT1A1 (TA)n genotype is not the major risk factor of cholelithiasis in sickle cell disease children. (9th January 2017)