Camaschella C - Search Results

1

The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload.

Camaschella C, Campanella A, De Falco L, Boschetto L, Merlini R, Silvestri L, Levi S, Iolascon A. Camaschella C, et al. Blood. 2007 Aug 15;110(4):1353-8. doi: 10.1182/blood-2007-02-072520. Epub 2007 May 7. Blood. 2007. PMID: 17485548 Free article.

2

Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosis.

Iolascon A, Miraglia del Giudice E, Camaschella C. Iolascon A, et al. Among authors: camaschella c. Haematologica. 1992 Jan-Feb;77(1):60-72. Haematologica. 1992. PMID: 1356891 Review.

3

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. 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.

4

Natural history of congenital dyserythropoietic anemia type II.

Iolascon A, Delaunay J, Wickramasinghe SN, Perrotta S, Gigante M, Camaschella C. Iolascon A, et al. Among authors: camaschella c. Blood. 2001 Aug 15;98(4):1258-60. doi: 10.1182/blood.v98.4.1258. Blood. 2001. PMID: 11493480 Free article.

5

Anemia and iron overload due to compound heterozygosity for novel ceruloplasmin mutations.

Bosio S, De Gobbi M, Roetto A, Zecchina G, Leonardo E, Rizzetto M, Lucetti C, Petrozzi L, Bonuccelli U, Camaschella C. Bosio S, et al. Among authors: camaschella c. Blood. 2002 Sep 15;100(6):2246-8. doi: 10.1182/blood-2002-02-0584. Blood. 2002. PMID: 12200392 Free article.

6

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: camaschella c. 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

7

Screening selected blood donors with biochemical iron overload for hemochromatosis: a regional experience.

De Gobbi M, D'Antico S, Castagno F, Testa D, Merlini R, Bondi A, Camaschella C. De Gobbi M, et al. Among authors: camaschella c. Haematologica. 2004 Oct;89(10):1161-7. Haematologica. 2004. PMID: 15477198

8

Understanding iron homeostasis through genetic analysis of hemochromatosis and related disorders.

Camaschella C. Camaschella C. Blood. 2005 Dec 1;106(12):3710-7. doi: 10.1182/blood-2005-05-1857. Epub 2005 Jul 19. Blood. 2005. PMID: 16030190 Free article. Review.

9

Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2).

Iolascon A, d'Apolito M, Servedio V, Cimmino F, Piga A, Camaschella C. Iolascon A, et al. Among authors: camaschella c. Blood. 2006 Jan 1;107(1):349-54. doi: 10.1182/blood-2005-06-2477. Epub 2005 Sep 13. Blood. 2006. PMID: 16160008 Free article.

10

Inherited hemochromatosis: from genetics to clinics.

Camaschella C, Merlini R. Camaschella C, et al. Minerva Med. 2005 Jun;96(3):207-22. Minerva Med. 2005. PMID: 16175162 Review. English, Italian.

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