Antonella Roetto
Antonella Roetto
Università di Torino. Dip Scienze Cliniche e Biologiche
Verified email at unito.it
Title
Cited by
Cited by
Year
Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis
A Roetto, G Papanikolaou, M Politou, F Alberti, D Girelli, J Christakis, ...
Nature genetics 33 (1), 21-22, 2003
10152003
The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22
C Camaschella, A Roetto, A Calì, M De Gobbi, G Garozzo, M Carella, ...
Nature genetics 25 (1), 14-15, 2000
9132000
Hepcidin is decreased in TFR2 hemochromatosis
E Nemeth, A Roetto, G Garozzo, T Ganz, C Camaschella
Blood 105 (4), 1803-1806, 2005
4432005
Mutation analysis of the HLA-H gene in Italian hemochromatosis patients.
M Carella, L D'ambrosio, A Totaro, A Grifa, MA Valentino, A Piperno, ...
American journal of human genetics 60 (4), 828, 1997
4151997
New mutations inactivating transferrin receptor 2 in hemochromatosis type 3
A Roetto, A Totaro, A Piperno, A Piga, F Longo, G Garozzo, A Calı̀, ...
Blood, The Journal of the American Society of Hematology 97 (9), 2555-2560, 2001
2762001
Heterogeneity of hemochromatosis in Italy
A Piperno, M Sampietro, A Pietrangelo, C Arosio, L Lupica, G Montosi, ...
Gastroenterology 114 (5), 996-1002, 1998
2751998
Juvenile hemochromatosis locus maps to chromosome 1q
A Roetto, A Totaro, M Cazzola, M Cicilano, S Bosio, G D'ascola, M Carella, ...
The American Journal of Human Genetics 64 (5), 1388-1393, 1999
2621999
Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis
C Lanzara, A Roetto, F Daraio, S Rivard, R Ficarella, H Simard, TM Cox, ...
Blood 103 (11), 4317-4321, 2004
2122004
Natural history of juvenile haemochromatosis
M De Gobbi, A Roetto, A Piperno, R Mariani, F Alberti, G Papanikolaou, ...
British journal of haematology 117 (4), 973-979, 2002
1862002
Juvenile hemochromatosis
C Camaschella, A Roetto, M De Gobbi
Seminars in hematology 39 (4), 242-248, 2002
154*2002
Clinical and pathologic findings in hemochromatosis type 3 due to a novel mutation in transferrin receptor 2 gene
D Girelli, C Bozzini, A Roetto, F Alberti, F Daraio, R Colombari, O Olivieri, ...
Gastroenterology 122 (5), 1295-1302, 2002
1542002
A valine deletion of ferroportin 1: a common mutation in hemochromatosis type 4?
A Roetto, AT Merryweather-Clarke, F Daraio, K Livesey, JJ Pointon, ...
Blood 100 (2), 733-734, 2002
1462002
Inherited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle Piastrine
CL Balduini, M Cattaneo, F Fabris, P Gresele, A Iolascon, FM Pulcinelli, ...
haematologica 88 (5), 582-592, 2003
1282003
Juvenile and adult hemochromatosis are distinct genetic disorders
C Camaschella, A Roetto, M Cicilano, P Pasquero, S Bosio, L Gubetta, ...
European Journal of Human Genetics 5, 371-375, 1997
1201997
Deferasirox is a powerful NF-κB inhibitor in myelodysplastic cells and in leukemia cell lines acting independently from cell iron deprivation by chelation and reactive oxygen …
E Messa, S Carturan, C Maffè, M Pautasso, E Bracco, A Roetto, F Messa, ...
Haematologica 95 (8), 1308-1316, 2010
1182010
Deferasirox treatment improved the hemoglobin level and decreased transfusion requirements in four patients with the myelodysplastic syndrome and primary myelofibrosis
E Messa, D Cilloni, F Messa, F Arruga, A Roetto, G Saglio
Acta haematologica 120 (2), 70-74, 2008
1112008
Screening hepcidin for mutations in juvenile hemochromatosis: identification of a new mutation (C70R)
A Roetto, F Daraio, P Porporato, R Caruso, TM Cox, M Cazzola, ...
Blood 103 (6), 2407-2409, 2004
1102004
Genetic interactions in thalassemia intermedia: analysis of β‐Mutations, α‐Genotype, γ‐Promoters, and β‐LCR hypersensitive sites 2 and 4 in Italian patients
C Camaschella, U Mazza, A Roetto, E Gottardl, A Parzlale, M Travl, ...
American journal of hematology 48 (2), 82-87, 1995
110*1995
Transferrin receptor 2 is a component of the erythropoietin receptor complex and is required for efficient erythropoiesis
H Forejtnikova, M Vieillevoye, Y Zermati, M Lambert, RM Pellegrino, ...
Blood, The Journal of the American Society of Hematology 116 (24), 5357-5367, 2010
1092010
The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients
A Piperno, C Arosio, S Fargion, A Roetto, C Nicoli, D Girelli, L Sbaiz, ...
Hepatology 24 (1), 43-46, 1996
751996
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