Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

281 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
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: camaschella c. Br J Haematol. 2005 Dec;131(5):663-70. doi: 10.1111/j.1365-2141.2005.05815.x. Br J Haematol. 2005. PMID: 16351644
Pathogenesis of hyperferritinemia cataract syndrome.
Roetto A, Bosio S, Gramaglia E, Barilaro MR, Zecchina G, Camaschella C. Roetto A, et al. Among authors: camaschella c. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):532-5. doi: 10.1006/bcmd.2002.0590. Blood Cells Mol Dis. 2002. PMID: 12547247
Increased serum hepcidin levels in subjects with the metabolic syndrome: a population study.
Martinelli N, Traglia M, Campostrini N, Biino G, Corbella M, Sala C, Busti F, Masciullo C, Manna D, Previtali S, Castagna A, Pistis G, Olivieri O, Toniolo D, Camaschella C, Girelli D. Martinelli N, et al. Among authors: camaschella c. PLoS One. 2012;7(10):e48250. doi: 10.1371/journal.pone.0048250. Epub 2012 Oct 29. PLoS One. 2012. PMID: 23144745 Free PMC article.
Rare types of genetic hemochromatosis.
Camaschella C, Poggiali E. Camaschella C, et al. Acta Haematol. 2009;122(2-3):140-5. doi: 10.1159/000243798. Epub 2009 Nov 10. Acta Haematol. 2009. PMID: 19907151
281 results