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Challenges and Opportunities of Precision Medicine in Sickle Cell Disease: Novel European Approach by GenoMed4All Consortium and ERN-EuroBloodNet.
Collado A, Boaro MP, van der Veen S, Idrizovic A, Biemond BJ, Beneitez Pastor D, Ortuño A, Cela E, Ruiz-Llobet A, Bartolucci P, de Montalembert M, Castellani G, Biondi R, Manara R, Sanavia T, Fariselli P, Kountouris P, Kleanthous M, Alvarez F, Zazo S, Colombatti R, van Beers EJ, Mañú-Pereira MDM. Collado A, et al. Among authors: bartolucci p. Hemasphere. 2023 Feb 22;7(3):e844. doi: 10.1097/HS9.0000000000000844. eCollection 2023 Mar. Hemasphere. 2023. PMID: 36844183 Free PMC article. No abstract available.
[Epidemiology of hemoglobin disorders].
Bartolucci P. Bartolucci P. Rev Prat. 2014 Oct;64(8):1108-9. Rev Prat. 2014. PMID: 25510136 French. No abstract available.
Multiple thrombosis in a patient with Gardos channelopathy and a new KCNN4 mutation.
Mansour-Hendili L, Egée S, Monedero-Alonso D, Bouyer G, Godeau B, Badaoui B, Lunati A, Noizat C, Aissat A, Kiger L, Mekki C, Picard V, Moutereau S, Fanen P, Bartolucci P, Garçon L, Galactéros F, Funalot B. Mansour-Hendili L, et al. Among authors: bartolucci p. Am J Hematol. 2021 Sep 1;96(9):E318-E321. doi: 10.1002/ajh.26245. Epub 2021 Jun 2. Am J Hematol. 2021. PMID: 34004026 Free article. No abstract available.
Extreme acute anemia in an adult sickle cell disease patient: look at the spleen.
de Prost N, Bartolucci P, Boroli F, Moroch J, Galactéros F, Brun-Buisson C, Thille AW. de Prost N, et al. Among authors: bartolucci p. Intensive Care Med. 2012 Feb;38(2):337-8. doi: 10.1007/s00134-011-2429-4. Epub 2011 Nov 26. Intensive Care Med. 2012. PMID: 22120771 No abstract available.
[Leukopenia and adult-onset Still's disease: two cases].
Rist S, Manceron V, Bartolucci P, Grasland A, Bosquet A, Vinceneux P. Rist S, et al. Among authors: bartolucci p. Rev Med Interne. 2005 Aug;26(8):670-2. doi: 10.1016/j.revmed.2005.04.031. Rev Med Interne. 2005. PMID: 15921827 French. No abstract available.
Exome sequencing for diagnosis of congenital hemolytic anemia.
Mansour-Hendili L, Aissat A, Badaoui B, Sakka M, Gameiro C, Ortonne V, Wagner-Ballon O, Pissard S, Picard V, Ghazal K, Bahuau M, Guitton C, Mansour Z, Duplan M, Petit A, Costedoat-Chalumeau N, Michel M, Bartolucci P, Moutereau S, Funalot B, Galactéros F. Mansour-Hendili L, et al. Among authors: bartolucci p. Orphanet J Rare Dis. 2020 Jul 8;15(1):180. doi: 10.1186/s13023-020-01425-5. Orphanet J Rare Dis. 2020. PMID: 32641076 Free PMC article.
175 results