Bartolucci, Pablo

Gene therapy in a patient with sickle cell disease

Ribeil, J.-A., Hacein-Bey-Abina, S., Payen, E., Magnani, A., Semeraro, M., Magrin, E., Caccavelli, L., Neven, B., Bourget, P., El Nemer, W., et al. (2017) · New England Journal of Medicine

Virus-based gene therapy researchHemoglobinopathies and Related Disorders

Cited by 696

Risk of autoimmune diseases and human papilloma virus (HPV) vaccines: six years of case-referent surveillance.

Grimaldi-Bensouda, L., Rossignol, M., Koné-Paut, I., Krivitzky, A., Lebrun-Frenay, C., Clet, J., Brassat, D., Papeix, C., Nicolino, M., Benhamou, P.-Y., et al. (2017) · Journal of Autoimmunity

Cervical Cancer and HPV ResearchPharmacovigilance and Adverse Drug Reactions

Cited by 84

Haematological determinants of cardiac involvement in adults with sickle cell disease

Damy, T., Bodez, D., Habibi, A., Guellich, A., Rappeneau, S., Inamo, J., Guendouz, S., Gellen-Dautremer, J., Pissard, S., Loric, S., et al. (2016) · European Heart Journal

Hemoglobinopathies and Related DisordersBlood groups and transfusion

Cited by 65

Allosteric control of hemoglobin S fiber formation by oxygen and its relation to the pathophysiology of sickle cell disease

Henry, E. R., Cellmer, T., Dunkelberger, E. B., Metaferia, B., Hofrichter, J., Li, Q., Ostrowski, D., Ghirlando, R., Louis, J. M., Moutereau, S., et al. (2020) · Proceedings of the National Academy of Sciences

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 65

Low fetal hemoglobin percentage is associated with silent brain lesions in adults with homozygous sickle cell disease

Calvet, D., Tuilier, T., Mélé, N., Turc, G., Habibi, A., Abdallah, N. A., Majhadi, L., Hemery, F., Edjlali, M., Galacteros, F., et al. (2017) · Blood Advances

Hemoglobinopathies and Related DisordersAdvanced MRI Techniques and Applications

Cited by 21