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Page 1
Retinal atrophy and markers of systemic and cerebrovascular severity in homozygous sickle cell disease.
Martin GC, Brousse V, Connes P, Grevent D, Kossorotoff M, Da Costa L, Bourdeau H, Charlot K, Boutonnat-Faucher B, Allali S, De Montalembert M, Bremond-Gignac D, Vidal PP, Robert MP. Martin GC, et al. Among authors: da costa l. Eur J Ophthalmol. 2022 Nov;32(6):3258-3266. doi: 10.1177/11206721221090794. Epub 2022 Mar 29. Eur J Ophthalmol. 2022. PMID: 35345916
Subtotal and total splenectomy for hereditary pyropoikilocytosis: Benefits and outcomes.
Pincez T, Guitton C, Landman-Parker J, Brousse V, Gauthier F, Da Costa L, Ghazal K, Dufillot D, Tchernia G, Picard V, Garçon L. Pincez T, et al. Among authors: da costa l. Am J Hematol. 2018 Oct;93(10):E340-E342. doi: 10.1002/ajh.25223. Epub 2018 Sep 26. Am J Hematol. 2018. PMID: 30035308 Free article. No abstract available.
Brain injury pathophysiology study by a multimodal approach in children with sickle cell anemia with no intra or extra cranial arteriopathy.
Brousse V, Pondarre C, Kossorotoff M, Arnaud C, Kamdem A, de Montalembert M, Boutonnat-Faucher B, Allali S, Bourdeau H, Charlot K, Bertil S, Da Costa L, Connes P, Grévent D, Verlhac S. Brousse V, et al. Among authors: da costa l. Haematologica. 2022 Apr 1;107(4):958-965. doi: 10.3324/haematol.2020.278226. Haematologica. 2022. PMID: 33882639 Free PMC article.
Biallelic mutations in the SARS2 gene presenting as congenital sideroblastic anemia.
Colin E, Courtois G, Brouzes C, Pulman J, Rabant M, Rötig A, Taffin H, Lion-Lambert M, Fabrega S, Da Costa L, De Montalembert M, Salomon R, Hermine O, Couronné L. Colin E, et al. Among authors: da costa l. Haematologica. 2021 Dec 1;106(12):3202-3205. doi: 10.3324/haematol.2021.279138. Haematologica. 2021. PMID: 34407605 Free PMC article. No abstract available.
Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer.
Da Costa L, Suner L, Galimand J, Bonnel A, Pascreau T, Couque N, Fenneteau O, Mohandas N; Society of Hematology and Pediatric Immunology (SHIP) group; French Society of Hematology (SFH). Da Costa L, et al. Blood Cells Mol Dis. 2016 Jan;56(1):9-22. doi: 10.1016/j.bcmd.2015.09.001. Epub 2015 Sep 16. Blood Cells Mol Dis. 2016. PMID: 26603718 Free PMC article.
Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experience.
Da Costa L, O'Donohue MF, van Dooijeweert B, Albrecht K, Unal S, Ramenghi U, Leblanc T, Dianzani I, Tamary H, Bartels M, Gleizes PE, Wlodarski M, MacInnes AW. Da Costa L, et al. Eur J Med Genet. 2018 Nov;61(11):664-673. doi: 10.1016/j.ejmg.2017.10.017. Epub 2017 Oct 26. Eur J Med Genet. 2018. PMID: 29081386 Free article. Review.
668 results