Levi S - Search Results

1

Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome.

Girelli D, Bozzini C, Zecchina G, Tinazzi E, Bosio S, Piperno A, Ramenghi U, Peters J, Levi S, Camaschella C, Corrocher R. Girelli D, et al. Among authors: levi s. Br J Haematol. 2001 Nov;115(2):334-40. doi: 10.1046/j.1365-2141.2001.03116.x. Br J Haematol. 2001. PMID: 11703332 Free article.

2

A new mutation (G51C) in the iron-responsive element (IRE) of L-ferritin associated with hyperferritinaemia-cataract syndrome decreases the binding affinity of the mutated IRE for iron-regulatory proteins.

Camaschella C, Zecchina G, Lockitch G, Roetto A, Campanella A, Arosio P, Levi S. Camaschella C, et al. Among authors: levi s. Br J Haematol. 2000 Mar;108(3):480-2. doi: 10.1046/j.1365-2141.2000.01920.x. Br J Haematol. 2000. PMID: 10759702 Free article.

3

Analysis of ferritins in lymphoblastoid cell lines and in the lens of subjects with hereditary hyperferritinemia-cataract syndrome.

Levi S, Girelli D, Perrone F, Pasti M, Beaumont C, Corrocher R, Albertini A, Arosio P. Levi S, et al. Blood. 1998 Jun 1;91(11):4180-7. Blood. 1998. PMID: 9596665 Free article.

4

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. Among authors: levi s. 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.

5

C29G in the iron-responsive element of L-ferritin: a new mutation associated with hyperferritinemia-cataract.

Bosio S, Campanella A, Gramaglia E, Porporato P, Longo F, Cremonesi L, Levi S, Camaschella C. Bosio S, et al. Among authors: levi s. Blood Cells Mol Dis. 2004 Jul-Aug;33(1):31-4. doi: 10.1016/j.bcmd.2004.04.010. Blood Cells Mol Dis. 2004. PMID: 15223007

6

Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolism.

Ferrari F, Foglieni B, Arosio P, Camaschella C, Daraio F, Levi S, García Erce JA, Beaumont C, Cazzola M, Ferrari M, Cremonesi L. Ferrari F, et al. Among authors: levi s. Hum Mutat. 2006 Feb;27(2):201-8. doi: 10.1002/humu.20294. Hum Mutat. 2006. PMID: 16395671

7

Case report: a subject with a mutation in the ATG start codon of L-ferritin has no haematological or neurological symptoms.

Cremonesi L, Cozzi A, Girelli D, Ferrari F, Fermo I, Foglieni B, Levi S, Bozzini C, Camparini M, Ferrari M, Arosio P. Cremonesi L, et al. Among authors: levi s. J Med Genet. 2004 Jun;41(6):e81. doi: 10.1136/jmg.2003.011718. J Med Genet. 2004. PMID: 15173247 Free PMC article. No abstract available.

8

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: levi s. 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.

9

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: levi 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.

10

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: levi s. 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.

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