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JAK2 (V617F) mutation in healthy individuals.
Passamonti F, Rumi E, Pietra D, Lazzarino M, Cazzola M. Passamonti F, et al. Among authors: pietra d. Br J Haematol. 2007 Feb;136(4):678-9. doi: 10.1111/j.1365-2141.2006.06483.x. Br J Haematol. 2007. PMID: 17223913 Free article. No abstract available.
Genetic and clinical heterogeneity of ferroportin disease.
Cremonesi L, Forni GL, Soriani N, Lamagna M, Fermo I, Daraio F, Galli A, Pietra D, Malcovati L, Ferrari M, Camaschella C, Cazzola M. Cremonesi L, et al. Among authors: pietra d. Br J Haematol. 2005 Dec;131(5):663-70. doi: 10.1111/j.1365-2141.2005.05815.x. Br J Haematol. 2005. PMID: 16351644 Free article.
Relation between JAK2 (V617F) mutation status, granulocyte activation, and constitutive mobilization of CD34+ cells into peripheral blood in myeloproliferative disorders.
Passamonti F, Rumi E, Pietra D, Della Porta MG, Boveri E, Pascutto C, Vanelli L, Arcaini L, Burcheri S, Malcovati L, Lazzarino M, Cazzola M. Passamonti F, et al. Among authors: pietra d. Blood. 2006 May 1;107(9):3676-82. doi: 10.1182/blood-2005-09-3826. Epub 2005 Dec 22. Blood. 2006. PMID: 16373657 Free article.
140 results