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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: soriani n. 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.
Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3).
Cazzola M, Cremonesi L, Papaioannou M, Soriani N, Kioumi A, Charalambidou A, Paroni R, Romtsou K, Levi S, Ferrari M, Arosio P, Christakis J. Cazzola M, et al. Among authors: soriani n. Br J Haematol. 2002 Nov;119(2):539-46. doi: 10.1046/j.1365-2141.2002.03946.x. Br J Haematol. 2002. PMID: 12406098 Free article.
COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma.
Galbiati S, Monguzzi A, Damin F, Soriani N, Passiu M, Castellani C, Natacci F, Curcio C, Seia M, Lalatta F, Chiari M, Ferrari M, Cremonesi L. Galbiati S, et al. Among authors: soriani n. J Med Genet. 2016 Jul;53(7):481-7. doi: 10.1136/jmedgenet-2015-103229. Epub 2016 Feb 24. J Med Genet. 2016. PMID: 26912453
Scanning mutations of the 5'UTR regulatory sequence of L-ferritin by denaturing high-performance liquid chromatography: identification of new mutations.
Cremonesi L, Paroni R, Foglieni B, Galbiati S, Fermo I, Soriani N, Belloli S, Ruggeri G, Biasiotto G, Cazzola M, Ferrari F, Ferrari M, Arosio P. Cremonesi L, et al. Among authors: soriani n. Br J Haematol. 2003 Apr;121(1):173-9. doi: 10.1046/j.1365-2141.2003.04253.x. Br J Haematol. 2003. PMID: 12670350 Free article.
51 results