Kolexia
Girot Robert
Médecine générale
Hôpital Necker Enfants Malades
Paris, France
66 Activités
0 Followers

Scientifique
Digital
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Expertise
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{{person.topmesh1.name}} Drépanocytose Anémie Hémolyse Infections bactériennes Maladies pulmonaires Albuminurie Ulcère Hypertension pulmonaire Hypertension artérielle

Industries

QualWorld
1 collaboration(s)
Dernière en 2018
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Dernières activités

Sickle cell disease, a genetic haemoglobin disease.
Revue de l'infirmiere   02 décembre 2021
Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease.
Frontiers in immunology   04 septembre 2020
An Evaluation of Three Ways of Communicating Carrier Status Results to the Parents of Children in a Neonatal Sickle Cell Screening Programme.
Frontiers in pediatrics   19 juin 2020
Polymorphisms in Inflammatory Genes Modulate the Occurrence of Clinical Complications in Patients with Sickle Cell Disease
Blood   13 novembre 2019
A Toll-like receptor 2 genetic variant modulates occurrence of bacterial infections in patients with sickle cell disease.
British journal of haematology   25 mars 2019
A Polymorphism in Toll-like Receptor 2 Gene Is Associated with Occurrence of Bacterial Infections in Sickle Cell Disease Patients
Blood   29 novembre 2018
Sickle SCAN™ (BioMedomics) fulfills analytical conditions for neonatal screening of sickle cell disease.
Annales de biologie clinique   05 novembre 2018
Evidence for the widespread use of neonatal screening for sickle cell disease.
Medecine sciences : M/S   16 avril 2018
Renin-angiotensin system blockade promotes a cardio-renal protection in albuminuric homozygous sickle cell patients.
British journal of haematology   19 octobre 2017
Factors predictive of leg-ulcer healing in sickle cell disease: a multicentre, prospective cohort study.
The British journal of dermatology   26 avril 2017