Camaschella C - Search Results

1

A Portuguese patient homozygous for the -25G>A mutation of the HAMP promoter shows evidence of steady-state transcription but fails to up-regulate hepcidin levels by iron.

Porto G, Roetto A, Daraio F, Pinto JP, Almeida S, Bacelar C, Nemeth E, Ganz T, Camaschella C. Porto G, et al. Among authors: camaschella c. Blood. 2005 Oct 15;106(8):2922-3. doi: 10.1182/blood-2005-04-1630. Blood. 2005. PMID: 16204153 Free article. No abstract available.

2

Variation in the phenotypic expression of C282Y hemochromatosis in an Italian family.

Bosio S, Zecchina G, Cicilano M, Roetto A, Salto AM, Camaschella C. Bosio S, et al. Among authors: camaschella c. Haematologica. 1999 Feb;84(2):184-5. Haematologica. 1999. PMID: 10091421 No abstract available.

3

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: camaschella c. Blood Cells Mol Dis. 2000 Jun;26(3):205-10. doi: 10.1006/bcmd.2000.0297. Blood Cells Mol Dis. 2000. PMID: 10950940

4

New mutations inactivating transferrin receptor 2 in hemochromatosis type 3.

Roetto A, Totaro A, Piperno A, Piga A, Longo F, Garozzo G, Calì A, De Gobbi M, Gasparini P, Camaschella C. Roetto A, et al. Among authors: camaschella c. Blood. 2001 May 1;97(9):2555-60. doi: 10.1182/blood.v97.9.2555. Blood. 2001. PMID: 11313241 Free article.

5

Linkage to chromosome 1q in Greek families with juvenile hemochromatosis.

Papanikolaou G, Politou M, Roetto A, Bosio S, Sakelaropoulos N, Camaschella C, Loukopoulos D. Papanikolaou G, et al. Among authors: camaschella c. Blood Cells Mol Dis. 2001 Jul-Aug;27(4):744-9. doi: 10.1006/bcmd.2001.0444. Blood Cells Mol Dis. 2001. PMID: 11778658

6

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: camaschella c. Gastroenterology. 2002 May;122(5):1295-302. doi: 10.1053/gast.2002.32984. Gastroenterology. 2002. PMID: 11984516

7

A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4.

Roetto A, Merryweather-Clarke AT, Daraio F, Livesey K, Pointon JJ, Barbabietola G, Piga A, Mackie PH, Robson KJ, Camaschella C. Roetto A, et al. Among authors: camaschella c. Blood. 2002 Jul 15;100(2):733-4. doi: 10.1182/blood-2002-03-0693. Blood. 2002. PMID: 12123233 Free article. No abstract available.

8

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.

9

Juvenile hemochromatosis.

Camaschella C, Roetto A, De Gobbi M. Camaschella C, et al. Semin Hematol. 2002 Oct;39(4):242-8. doi: 10.1053/shem.2002.35635. Semin Hematol. 2002. PMID: 12382199 Review.

10

Genetic haemochromatosis: genes and mutations associated with iron loading.

Camaschella C, Roetto A, De Gobbi M. Camaschella C, et al. Best Pract Res Clin Haematol. 2002 Jun;15(2):261-76. doi: 10.1016/s1521-6926(02)90207-0. Best Pract Res Clin Haematol. 2002. PMID: 12401307 Review.

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