Robert Girot

4 Rue De La Chine
Paris, 75020, France

Last Updated: 09/26/2026

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Found 25 publications

Splenectomy in β-thalassemia patients: Practices and risks in a nationwide study.

Splenectomy in β-thalassemia patients: Practices and risks in a nationwide study.

Journal: HemaSphere

Published: November 26, 2025

Sickle cell disease, a genetic haemoglobin disease

Sickle cell disease, a genetic haemoglobin disease

Journal: Revue de l'infirmiere

Published: January 29, 2022

Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease.

Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease.

Journal: Frontiers in immunology

Published: April 20, 2020

An Evaluation of Three Ways of Communicating Carrier Status Results to the Parents of Children in a Neonatal Sickle Cell Screening Programme.

An Evaluation of Three Ways of Communicating Carrier Status Results to the Parents of Children in a Neonatal Sickle Cell Screening Programme.

Journal: Frontiers in pediatrics

Published: December 09, 2019

A Toll-like receptor 2 genetic variant modulates occurrence of bacterial infections in patients with sickle cell disease.

A Toll-like receptor 2 genetic variant modulates occurrence of bacterial infections in patients with sickle cell disease.

Journal: British journal of haematology

Published: November 23, 2018

Sickle SCAN™ (BioMedomics) fulfills analytical conditions for neonatal screening of sickle cell disease.

Sickle SCAN™ (BioMedomics) fulfills analytical conditions for neonatal screening of sickle cell disease.

Journal: Annales de biologie clinique

Published: July 07, 2018

Evidence for the widespread use of neonatal screening for sickle cell disease

Evidence for the widespread use of neonatal screening for sickle cell disease

Journal: Medecine sciences : M/S

Published: April 17, 2018

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

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

Journal: British journal of haematology

Published: June 27, 2017

Family cord blood banking for sickle cell disease: a twenty-year experience in two dedicated public cord blood banks.

Family cord blood banking for sickle cell disease: a twenty-year experience in two dedicated public cord blood banks.

Journal: Haematologica

Published: December 24, 2016

Factors predictive of leg-ulcer healing in sickle cell disease: a multicentre, prospective cohort study.

Factors predictive of leg-ulcer healing in sickle cell disease: a multicentre, prospective cohort study.

Journal: The British journal of dermatology

Published: December 07, 2016

Iron restriction is an important treatment of hemoglobin SC disease.

Iron restriction is an important treatment of hemoglobin SC disease.

Journal: American journal of hematology

Published: March 24, 2016

Plasma therapy against infectious pathogens, as of yesterday, today and tomorrow.

Plasma therapy against infectious pathogens, as of yesterday, today and tomorrow.

Journal: Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine

Published: December 04, 2015

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Last Updated: 09/26/2026