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Recommendations for diagnosis and treatment of methemoglobinemia.
Iolascon A, Bianchi P, Andolfo I, Russo R, Barcellini W, Fermo E, Toldi G, Ghirardello S, Rees D, Van Wijk R, Kattamis A, Gallagher PG, Roy N, Taher A, Mohty R, Kulozik A, De Franceschi L, Gambale A, De Montalembert M, Forni GL, Harteveld CL, Prchal J; SWG of red cell and iron of EHA and EuroBloodNet. Iolascon A, et al. Among authors: barcellini w. Am J Hematol. 2021 Dec 1;96(12):1666-1678. doi: 10.1002/ajh.26340. Epub 2021 Sep 23. Am J Hematol. 2021. PMID: 34467556 Free PMC article. Review.
CDAII presenting as hydrops foetalis: molecular characterization of two cases.
Fermo E, Bianchi P, Notarangelo LD, Binda S, Vercellati C, Marcello AP, Boschetti C, Barcellini W, Zanella A. Fermo E, et al. Among authors: barcellini w. Blood Cells Mol Dis. 2010 Jun 15;45(1):20-2. doi: 10.1016/j.bcmd.2010.03.005. Epub 2010 Apr 9. Blood Cells Mol Dis. 2010. PMID: 20381388
Hereditary red cell membrane defects: diagnostic and clinical aspects.
Barcellini W, Bianchi P, Fermo E, Imperiali FG, Marcello AP, Vercellati C, Zaninoni A, Zanella A. Barcellini W, et al. Blood Transfus. 2011 Jul;9(3):274-7. doi: 10.2450/2011.0086-10. Epub 2011 Jan 13. Blood Transfus. 2011. PMID: 21251470 Free PMC article. Review. No abstract available.
296 results