Cazzola M - Search Results

1

Denaturing HPLC analysis of DNA deletions and insertions.

Cremonesi L, Stenirri S, Fermo I, Paroni R, Ferrari M, Cazzola M, Arosio P. Cremonesi L, et al. Among authors: cazzola m. Hum Mutat. 2003 Jul;22(1):98-102. doi: 10.1002/humu.10234. Hum Mutat. 2003. PMID: 12815600

2

Manipulations of cellular iron metabolism for modulating normal and malignant cell proliferation: achievements and prospects.

Cazzola M, Bergamaschi G, Dezza L, Arosio P. Cazzola M, et al. Blood. 1990 May 15;75(10):1903-19. Blood. 1990. PMID: 2186818 Free article. Review. No abstract available.

3

Immunocytochemical detection of ferritin in human bone marrow and peripheral blood cells using monoclonal antibodies specific for the H and L subunit.

Invernizzi R, Cazzola M, De Fazio P, Rosti V, Ruggeri G, Arosio P. Invernizzi R, et al. Among authors: cazzola m. Br J Haematol. 1990 Nov;76(3):427-32. doi: 10.1111/j.1365-2141.1990.tb06379.x. Br J Haematol. 1990. PMID: 2261353

4

Hereditary hyperferritinemia-cataract syndrome: relationship between phenotypes and specific mutations in the iron-responsive element of ferritin light-chain mRNA.

Cazzola M, Bergamaschi G, Tonon L, Arbustini E, Grasso M, Vercesi E, Barosi G, Bianchi PE, Cairo G, Arosio P. Cazzola M, et al. Blood. 1997 Jul 15;90(2):814-21. Blood. 1997. PMID: 9226182 Free article.

5

A novel deletion of the L-ferritin iron-responsive element responsible for severe hereditary hyperferritinaemia-cataract syndrome.

Cazzola M, Foglieni B, Bergamaschi G, Levi S, Lazzarino M, Arosio P. Cazzola M, et al. Br J Haematol. 2002 Mar;116(3):667-70. doi: 10.1046/j.0007-1048.2001.03310.x. Br J Haematol. 2002. PMID: 11849230 Free article.

6

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. 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.

7

Mitochondrial ferritin: a new player in iron metabolism.

Drysdale J, Arosio P, Invernizzi R, Cazzola M, Volz A, Corsi B, Biasiotto G, Levi S. Drysdale J, et al. Among authors: cazzola m. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):376-83. doi: 10.1006/bcmd.2002.0577. Blood Cells Mol Dis. 2002. PMID: 12547228 Review.

8

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: cazzola m. 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.

9

Ferroportin gene silencing induces iron retention and enhances ferritin synthesis in human macrophages.

Gallí A, Bergamaschi G, Recalde H, Biasiotto G, Santambrogio P, Boggi S, Levi S, Arosio P, Cazzola M. Gallí A, et al. Among authors: cazzola m. Br J Haematol. 2004 Dec;127(5):598-603. doi: 10.1111/j.1365-2141.2004.05238.x. Br J Haematol. 2004. PMID: 15566364 Free article.

10

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: cazzola m. 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.

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