Alberti F - Search Results

1

Clinical and pathologic findings in hemochromatosis type 3 due to a novel mutation in transferrin receptor 2 gene.

Girelli D, Bozzini C, Roetto A, Alberti F, Daraio F, Colombari R, Olivieri O, Corrocher R, Camaschella C. Girelli D, et al. Among authors: alberti f. Gastroenterology. 2002 May;122(5):1295-302. doi: 10.1053/gast.2002.32984. Gastroenterology. 2002. PMID: 11984516

2

Hemochromatosis due to mutations in transferrin receptor 2.

Roetto A, Daraio F, Alberti F, Porporato P, Calì A, De Gobbi M, Camaschella C. Roetto A, et al. Among authors: alberti f. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):465-70. doi: 10.1006/bcmd.2002.0585. Blood Cells Mol Dis. 2002. PMID: 12547237

3

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis.

Roetto A, Papanikolaou G, Politou M, Alberti F, Girelli D, Christakis J, Loukopoulos D, Camaschella C. Roetto A, et al. Among authors: alberti f. Nat Genet. 2003 Jan;33(1):21-2. doi: 10.1038/ng1053. Epub 2002 Dec 9. Nat Genet. 2003. PMID: 12469120

4

Exclusion of ZIRTL as candidate gene of juvenile hemochromatosis and refinement of the critical interval on 1q21.

Roetto A, Alberti F, Daraio F, Cali A, Cazzola M, Totaro A, Gasparini P, Camaschella C. Roetto A, et al. Among authors: alberti f. Blood Cells Mol Dis. 2000 Jun;26(3):205-10. doi: 10.1006/bcmd.2000.0297. Blood Cells Mol Dis. 2000. PMID: 10950940

5

Natural history of juvenile haemochromatosis.

De Gobbi M, Roetto A, Piperno A, Mariani R, Alberti F, Papanikolaou G, Politou M, Lockitch G, Girelli D, Fargion S, Cox TM, Gasparini P, Cazzola M, Camaschella C. De Gobbi M, et al. Among authors: alberti f. Br J Haematol. 2002 Jun;117(4):973-9. doi: 10.1046/j.1365-2141.2002.03509.x. Br J Haematol. 2002. PMID: 12060140 Free article. Review.

6

Structural, functional, and tissue distribution analysis of human transferrin receptor-2 by murine monoclonal antibodies and a polyclonal antiserum.

Deaglio S, Capobianco A, Calì A, Bellora F, Alberti F, Righi L, Sapino A, Camaschella C, Malavasi F. Deaglio S, et al. Among authors: alberti f. Blood. 2002 Nov 15;100(10):3782-9. doi: 10.1182/blood-2002-01-0076. Epub 2002 Jul 5. Blood. 2002. PMID: 12393650 Free article.

7

TFR2 Y250X mutation in Italy.

De Gobbi M, Barilaro MR, Garozzo G, Sbaiz L, Alberti F, Camaschella C. De Gobbi M, et al. Among authors: alberti f. Br J Haematol. 2001 Jul;114(1):243-4. doi: 10.1046/j.1365-2141.2001.02873-3.x. Br J Haematol. 2001. PMID: 11472377 Free article. No abstract available.

8

A new mutation trans to I278T cystathionine beta-synthase associated with Factor V Leiden causes mild homocystinuria but severe vascular disease.

Bosio S, Cavallero G, Brusa E, Alberti F, Camaschella C. Bosio S, et al. Among authors: alberti f. Thromb Haemost. 2001 Aug;86(2):716-7. Thromb Haemost. 2001. PMID: 11522031 No abstract available.

9

Quantitative assessment of minimal residual disease in acute myeloid leukemia carrying nucleophosmin (NPM1) gene mutations.

Gorello P, Cazzaniga G, Alberti F, Dell'Oro MG, Gottardi E, Specchia G, Roti G, Rosati R, Martelli MF, Diverio D, Lo Coco F, Biondi A, Saglio G, Mecucci C, Falini B. Gorello P, et al. Among authors: alberti f. Leukemia. 2006 Jun;20(6):1103-8. doi: 10.1038/sj.leu.2404149. Leukemia. 2006. PMID: 16541144

10

Pan-neuronal expression of human mutant SOD1 in Drosophila impairs survival and motor performance, induces early neuroinflammation and chromosome aberrations.

Liguori F, Alberti F, Amadio S, Angelini DF, Pilesi E, Vitale G, Tesoriere G, Borsellino G, Vernì F, Volonté C. Liguori F, et al. Among authors: alberti f. Biochim Biophys Acta Mol Basis Dis. 2024 Apr 22;1870(5):167192. doi: 10.1016/j.bbadis.2024.167192. Online ahead of print. Biochim Biophys Acta Mol Basis Dis. 2024. PMID: 38657911

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