Roetto A - Search Results

1

Hemochromatosis due to mutations in transferrin receptor 2.

Roetto A, Daraio F, Alberti F, Porporato P, Calì A, De Gobbi M, Camaschella C. Roetto A, et al. Blood Cells Mol Dis. 2002 Nov-Dec;29(3):465-70. doi: 10.1006/bcmd.2002.0585. Blood Cells Mol Dis. 2002. PMID: 12547237

2

New polymorphisms and markers in the HLA class I region: relevance to hereditary hemochromatosis (HFE).

Totaro A, Grifa A, Roetto A, Lunardi C, D'Agruma L, Sbaiz L, Zelante L, De Sandre G, Camaschella C, Gasparini P. Totaro A, et al. Among authors: roetto a. Hum Genet. 1995 Apr;95(4):429-34. doi: 10.1007/BF00208969. Hum Genet. 1995. PMID: 7705840

3

Beta-myosin mutations in hypertrophic cardiomyopathies.

Alfarano A, Gastaldi L, Tos GG, Roetto A, Camaschella C. Alfarano A, et al. Among authors: roetto a. 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.

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: roetto a. 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: roetto a. Hepatology. 1996 Jul;24(1):43-6. doi: 10.1053/jhep.1996.v24.pm0008707280. Hepatology. 1996. PMID: 8707280 Free article.

6

Allelic association of microsatellites of 6p in Italian hemochromatosis patients.

Camaschella C, Roetto A, Gasparini P, Piperno A, Fortina P, Surrey S, Rappaport E. Camaschella C, et al. Among authors: roetto a. Hum Genet. 1996 Apr;97(4):476-81. doi: 10.1007/BF02267070. Hum Genet. 1996. PMID: 8834246 Free article.

7

Hereditary hemochromatosis: generation of a transcription map within a refined and extended map of the HLA class I region.

Totaro A, Rommens JM, Grifa A, Lunardi C, Carella M, Huizenga JJ, Roetto A, Camaschella C, De Sandre G, Gasparini P. Totaro A, et al. Among authors: roetto a. Genomics. 1996 Feb 1;31(3):319-26. doi: 10.1006/geno.1996.0054. Genomics. 1996. PMID: 8838313

8

Serum erythropoietin and circulating transferrin receptor in thalassemia intermedia patients with heterogeneous genotypes.

Camaschella C, Gonella S, Calabrese R, Vischia F, Roetto A, Graziadei G, Mazza U, Cappellini MD. Camaschella C, et al. Among authors: roetto a. Haematologica. 1996 Sep-Oct;81(5):397-403. Haematologica. 1996. PMID: 8952151

9

Two polymorphic repeats in the candidate region for the haemochromatosis gene.

Grifa A, Totaro A, Carella M, D'Ambrosio L, Sbaiz L, Roetto A, Camaschella C, Gasparini P. Grifa A, et al. Among authors: roetto a. Mol Cell Probes. 1996 Dec;10(6):469-70. doi: 10.1006/mcpr.1996.0065. Mol Cell Probes. 1996. PMID: 9025086 No abstract available.

10

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: roetto a. Am J Hum Genet. 1997 Apr;60(4):828-32. Am J Hum Genet. 1997. PMID: 9106528 Free PMC article.

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