Majore S - Search Results

1

Unexplained isolated hyperferritinemia without iron overload.

Ravasi G, Pelucchi S, Mariani R, Casati M, Greni F, Arosio C, Pelloni I, Majore S, Santambrogio P, Levi S, Piperno A. Ravasi G, et al. Among authors: majore s. Am J Hematol. 2017 Apr;92(4):338-343. doi: 10.1002/ajh.24641. Epub 2017 Feb 7. Am J Hematol. 2017. PMID: 28052375 Free article.

2

Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload.

Majore S, Milano F, Binni F, Stuppia L, Cerrone A, Tafuri A, De Bernardo C, Palka G, Grammatico P. Majore S, et al. Haematologica. 2006 Aug;91(8 Suppl):ECR33. Haematologica. 2006. PMID: 16923517

3

Radio FC, Majore S, Binni F, Valiante M, Ricerca BM, De Bernardo C, Morrone A, Grammatico P. Radio FC, et al. Among authors: majore s. Blood Cells Mol Dis. 2014 Feb-Mar;52(2-3):83-7. doi: 10.1016/j.bcmd.2013.08.003. Epub 2013 Sep 20. Blood Cells Mol Dis. 2014. PMID: 24055163

4

Hyperferritinemia-cataract syndrome: Long-term ophthalmic observations in an Italian family.

Cosentino I, Zeri F, Swann PG, Majore S, Radio FC, Palumbo P, Grammatico P, Petitti V. Cosentino I, et al. Among authors: majore s. Ophthalmic Genet. 2016 Sep;37(3):318-22. doi: 10.3109/13816810.2015.1059460. Epub 2016 Feb 5. Ophthalmic Genet. 2016. PMID: 26849797

5

Characterization of three novel pathogenic SLC40A1 mutations and genotype/phenotype correlations in 7 Italian families with type 4 hereditary hemochromatosis.

Majore S, Bonaccorsi di Patti MC, Valiante M, Polticelli F, Cortese A, Di Bartolomeo S, De Bernardo C, De Muro M, Faienza F, Radio FC, Grammatico P, Musci G. Majore S, et al. Biochim Biophys Acta Mol Basis Dis. 2018 Feb;1864(2):464-470. doi: 10.1016/j.bbadis.2017.11.006. Epub 2017 Nov 14. Biochim Biophys Acta Mol Basis Dis. 2018. PMID: 29154924 Free article.

6

Structural modeling of a novel TERC variant in a patient with aplastic anemia and short telomeres.

Rinelli M, Bellacchio E, Berardinelli F, Pascolini G, Grammatico P, Sgura A, Iori AP, Quattrocchi L, Novelli A, Majore S, Agolini E. Rinelli M, et al. Among authors: majore s. Ann Hematol. 2019 Mar;98(3):805-807. doi: 10.1007/s00277-018-3415-5. Epub 2018 Jul 6. Ann Hematol. 2019. PMID: 29980875 No abstract available.

7

Correction to: Structural modeling of a novel TERC variant in a patient with aplastic anemia and short telomeres.

Rinelli M, Bellacchio E, Berardinelli F, Pascolini G, Grammatico P, Sgura A, Iori AP, Quattrocchi L, Novelli A, Majore S, Agolini E. Rinelli M, et al. Among authors: majore s. Ann Hematol. 2019 Mar;98(3):809. doi: 10.1007/s00277-018-3581-5. Ann Hematol. 2019. PMID: 30552465

8

Novel and recurrent p14 mutations in Italian familial melanoma.

Binni F, Antigoni I, De Simone P, Majore S, Silipo V, Crisi A, Amantea A, Pacchiarini D, Castori M, De Bernardo C, Catricalà C, Grammatico P. Binni F, et al. Among authors: majore s. Clin Genet. 2010 Jun;77(6):581-6. doi: 10.1111/j.1399-0004.2009.01298.x. Epub 2010 Feb 4. Clin Genet. 2010. PMID: 20132244

9

ATP2C1 gene mutation analysis in Italian patients with Hailey-Hailey disease.

Majore S, Biolcati G, Barboni L, Cannistraci C, Binni F, Crisi A, Picardo M, Grammatico P. Majore S, et al. J Invest Dermatol. 2005 Nov;125(5):933-5. doi: 10.1111/j.0022-202X.2005.23941.x. J Invest Dermatol. 2005. PMID: 16297192 Free article.

10

Association of hepcidin promoter c.-582 A>G variant and iron overload in thalassemia major.

Andreani M, Radio FC, Testi M, De Bernardo C, Troiano M, Majore S, Bertucci P, Polchi P, Rosati R, Grammatico P. Andreani M, et al. Among authors: majore s. Haematologica. 2009 Sep;94(9):1293-6. doi: 10.3324/haematol.2009.006270. Haematologica. 2009. PMID: 19734422 Free PMC article.

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