Camaschella C - Search Results

1

Pathogenesis of hyperferritinemia cataract syndrome.

Roetto A, Bosio S, Gramaglia E, Barilaro MR, Zecchina G, Camaschella C. Roetto A, et al. Among authors: camaschella c. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):532-5. doi: 10.1006/bcmd.2002.0590. Blood Cells Mol Dis. 2002. PMID: 12547247

2

Beta-myosin mutations in hypertrophic cardiomyopathies.

Alfarano A, Gastaldi L, Tos GG, Roetto A, Camaschella C. Alfarano A, et al. Among authors: camaschella c. Ann N Y Acad Sci. 1995 Mar 27;752:227-9. doi: 10.1111/j.1749-6632.1995.tb17429.x. Ann N Y Acad Sci. 1995. PMID: 7755266 No abstract available.

3

Genetic interactions in thalassemia intermedia: analysis of beta-mutations, alpha-genotype, gamma-promoters, and beta-LCR hypersensitive sites 2 and 4 in Italian patients.

Camaschella C, Mazza U, Roetto A, Gottardi E, Parziale A, Travi M, Fattore S, Bacchiega D, Fiorelli G, Cappellini MD. Camaschella C, et al. Am J Hematol. 1995 Feb;48(2):82-7. doi: 10.1002/ajh.2830480203. Am J Hematol. 1995. PMID: 7847345

4

Analysis of microsatellite instability in chronic lymphoproliferative disorders.

Volpe G, Gamberi B, Pastore C, Roetto A, Pautasso M, Parvis G, Camaschella C, Mazza U, Saglio G, Gaidano G. Volpe G, et al. Among authors: camaschella c. Ann Hematol. 1996 Feb;72(2):67-71. doi: 10.1007/BF00641310. Ann Hematol. 1996. PMID: 8597609 Free article.

5

The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients.

Piperno A, Arosio C, Fargion S, Roetto A, Nicoli C, Girelli D, Sbaiz L, Gasparini P, Boari G, Sampietro M, Camaschella C. Piperno A, et al. Among authors: camaschella c. Hepatology. 1996 Jul;24(1):43-6. doi: 10.1053/jhep.1996.v24.pm0008707280. Hepatology. 1996. PMID: 8707280 Free article.

6

Mutation analysis of the HLA-H gene in Italian hemochromatosis patients.

Carella M, D'Ambrosio L, Totaro A, Grifa A, Valentino MA, Piperno A, Girelli D, Roetto A, Franco B, Gasparini P, Camaschella C. Carella M, et al. Among authors: camaschella c. Am J Hum Genet. 1997 Apr;60(4):828-32. Am J Hum Genet. 1997. PMID: 9106528 Free PMC article.

7

A frequent polymorphism in the 5' region of the BCMA gene.

Roetto A, Cicilano M, Gottardi E, Totaro A, Carella M, Gasparini P, Camaschella C. Roetto A, et al. Among authors: camaschella c. Mol Cell Probes. 1997 Aug;11(4):311-2. doi: 10.1006/mcpr.1997.0115. Mol Cell Probes. 1997. PMID: 9281419 No abstract available.

8

A recombination event close to HFE gene in hereditary hemochromatosis.

Roetto A, Sbaiz L, Bosio S, Piperno A, Fargion S, Carella M, Totaro A, Grifa A, Gasparini P, Camaschella C. Roetto A, et al. Among authors: camaschella c. Ann Genet. 1997;40(3):150-3. Ann Genet. 1997. PMID: 9401103 Free article.

9

Feasibility of molecular diagnosis of alpha-thalassemia in the evaluation of microcytosis.

Sivera P, Roetto A, Mazza U, Camaschella C. Sivera P, et al. Among authors: camaschella c. Haematologica. 1997 Sep-Oct;82(5):592-3. Haematologica. 1997. PMID: 9407728 Free article.

10

Juvenile and adult hemochromatosis are distinct genetic disorders.

Camaschella C, Roetto A, Cicilano M, Pasquero P, Bosio S, Gubetta L, Di Vito F, Girelli D, Totaro A, Carella M, Grifa A, Gasparini P. Camaschella C, et al. Eur J Hum Genet. 1997 Nov-Dec;5(6):371-5. Eur J Hum Genet. 1997. PMID: 9450181

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