Robert Girot

Zoetis (United States) — United States

Medicine · Health Sciences

47h-index8.0kcitations326works0.02yr avg
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Research Topics

Hemoglobinopathies and Related Disorders(213), Iron Metabolism and Disorders(92), Blood groups and transfusion(74), Erythrocyte Function and Pathophysiology(50), Parvovirus B19 Infection Studies(22)

Publications326 total

Etude d’écoconception d’un procédé de toiture stockante
SPIRE - Sciences Po Institutional REpository·2024Open Access
Les auteurs
Elsevier eBooks·2022Open Access
La drépanocytose, une maladie génétique de l’hémoglobine
La Revue de l Infirmière·2021· 1 citedOpen Access
Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease
Frontiers in Immunology·2020· 19 citedOpen Access
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·2020· 3 citedOpen Access
Polymorphisms in Inflammatory Genes Modulate the Occurrence of Clinical Complications in Patients with Sickle Cell Disease
Blood·2019
A Toll‐like receptor 2 genetic variant modulates occurrence of bacterial infections in patients with sickle cell disease
British Journal of Haematology·2019· 11 citedOpen Access
A Polymorphism in Toll-like Receptor 2 Gene Is Associated with Occurrence of Bacterial Infections in Sickle Cell Disease Patients
Blood·2018· 1 cited
Sickle SCAN™ (BioMedomics) fulfills analytical conditions for neonatal screening of sickle cell disease
Annales de biologie clinique·2018· 17 cited
Dépistage néonatal de la drépanocytose
médecine/sciences·2018· 6 citedOpen Access
Renin‐angiotensin system blockade promotes a cardio‐renal protection in albuminuric homozygous sickle cell patients
British Journal of Haematology·2017· 19 citedOpen Access
Les porteurs du trait drépanocytaire AS
2017
Family cord blood banking for sickle cell disease: a twenty-year experience in two dedicated public cord blood banks
Haematologica·2017· 14 citedOpen Access
Factors predictive of leg-ulcer healing in sickle cell disease: a multicentre, prospective cohort study
British Journal of Dermatology·2016· 35 cited
Hydroxycarbamide (HU), Sickle Cell Disease and Pregnancy, a Multicentric Retrospective Study
Blood·2016· 3 cited
Hemoglobin S Screening Using the « Sickle Scan » - Biomedomics System. the Necker-Enfants Malades Hospital Experience
Blood·2016· 2 cited
Maladies auto-immunes au cours des syndromes drépanocytaires majeurs : étude de 26 cas
La Revue de Médecine Interne·2016· 1 cited
Iron restriction is an important treatment of hemoglobin SC disease
American Journal of Hematology·2016· 9 citedOpen Access
La drépanocytose en France
Revue Francophone des Laboratoires·2016· 14 cited
Pronostic de cicatrisation et de récidive des ulcères drépanocytaires : étude multicentrique prospective française
Journal des Maladies Vasculaires·2016
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Frequent Co-authors

François Lionnet(9), Micheline Maïer-Redelsperger(9), Jacques Élion(8), Rolande Ducrocq(6), Martine Mariotti(6), Jean‐Jacques Lefrère(6), François Lefrère(5), Mariane de Montalembert(5), Joëlle Lerable(5), M. de Montalembert(4), Françoise Roudot‐Thoraval(4), Guillaume Lefèvre(4), Françoise Bernaudin(3), Frédéric Galactéros(3), Dora Bachir(3), V. Avellino(3), Jean‐Philippe Haymann(3), K. Stankovic(3), Pierre Lévy(3), Pierre‐Louis Tharaux(3)