Totaro A - Search Results

1

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

2

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: totaro a. Ann Genet. 1997;40(3):150-3. Ann Genet. 1997. PMID: 9401103 Free article.

3

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. Among authors: totaro a. Eur J Hum Genet. 1997 Nov-Dec;5(6):371-5. Eur J Hum Genet. 1997. PMID: 9450181

4

Juvenile hemochromatosis locus maps to chromosome 1q.

Roetto A, Totaro A, Cazzola M, Cicilano M, Bosio S, D'Ascola G, Carella M, Zelante L, Kelly AL, Cox TM, Gasparini P, Camaschella C. Roetto A, et al. Among authors: totaro a. Am J Hum Genet. 1999 May;64(5):1388-93. doi: 10.1086/302379. Am J Hum Genet. 1999. PMID: 10205270 Free PMC article.

5

The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.

Camaschella C, Roetto A, Calì A, De Gobbi M, Garozzo G, Carella M, Majorano N, Totaro A, Gasparini P. Camaschella C, et al. Among authors: totaro a. Nat Genet. 2000 May;25(1):14-5. doi: 10.1038/75534. Nat Genet. 2000. PMID: 10802645

6

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: totaro a. Blood. 2001 May 1;97(9):2555-60. doi: 10.1182/blood.v97.9.2555. Blood. 2001. PMID: 11313241 Free article.

7

Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes.

Lanzara C, Ficarella R, Totaro A, Chen X, Roberto R, Perrotta S, Lasalandra C, Gasparini P, Iolascon A, Carella M. Lanzara C, et al. Among authors: totaro a. Blood Cells Mol Dis. 2003 Jan-Feb;30(1):22-9. doi: 10.1016/s1079-9796(03)00009-3. Blood Cells Mol Dis. 2003. PMID: 12667984

8

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. Hum Genet. 1995 Apr;95(4):429-34. doi: 10.1007/BF00208969. Hum Genet. 1995. PMID: 7705840

9

Construction of a genetic map telomeric to HLA-A by microsatellite analysis.

Camaschella C, Roetto A, De Sandre G, Piperno A, Totaro A, Dianzani I, Gasparini P. Camaschella C, et al. Among authors: totaro a. Mol Cell Probes. 1993 Oct;7(5):411-4. doi: 10.1006/mcpr.1993.1060. Mol Cell Probes. 1993. PMID: 8264675

10

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: totaro 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.

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