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A Roetto

Showing results (1-10 of 32) with videos related to

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Haematologica|January 4, 1998
Feasibility of molecular diagnosis of alpha-thalassemia in the evaluation of microcytosisP Sivera, A Roetto, U Mazza, et al.
Human Genetics|November 1, 1994
A new complex polymorphic repeat close to the HLA-A and HLA-E lociA Totaro, A Grifa, A Roetto, et al.
Blood Cells, Molecules & Diseases|June 22, 2005
Juvenile hemochromatosis due to G320V/Q116X compound heterozygosity of hemojuvelin in an Irish patientF Daraio, E Ryan, F Gleeson, et al.
Acta Haematologica|October 2, 2008
Deferasirox treatment improved the hemoglobin level and decreased transfusion requirements in four patients with the myelodysplastic syndrome and primary myelofibrosisE Messa, D Cilloni, F Messa, et al.
Blood Cells, Molecules & Diseases|January 10, 2002
Linkage to chromosome 1q in Greek families with juvenile hemochromatosisG Papanikolaou, M Politou, A Roetto, et al.
British Journal of Haematology|April 12, 2000
A new mutation (G51C) in the iron-responsive element (IRE) of L-ferritin associated with hyperferritinaemia-cataract syndrome decreases the binding affinity of the mutated IRE for iron-regulatory proteinsC Camaschella, G Zecchina, G Lockitch, et al.
Human Genetics|April 1, 1996
Allelic association of microsatellites of 6p in Italian hemochromatosis patientsC Camaschella, A Roetto, P Gasparini, et al.
Haematologica|June 15, 1999
Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndromeM Cicilano, G Zecchina, A Roetto, et al.
Molecular and Cellular Probes|October 1, 1993
Construction of a genetic map telomeric to HLA-A by microsatellite analysisC Camaschella, A Roetto, G De Sandre, et al.
Blood Cells, Molecules & Diseases|August 22, 2000
Exclusion of ZIRTL as candidate gene of juvenile hemochromatosis and refinement of the critical interval on 1q21A Roetto, F Alberti, F Daraio, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Haematologica|January 4, 1998
Feasibility of molecular diagnosis of alpha-thalassemia in the evaluation of microcytosisP Sivera, A Roetto, U Mazza, et al.
Human Genetics|November 1, 1994
A new complex polymorphic repeat close to the HLA-A and HLA-E lociA Totaro, A Grifa, A Roetto, et al.
Blood Cells, Molecules & Diseases|June 22, 2005
Juvenile hemochromatosis due to G320V/Q116X compound heterozygosity of hemojuvelin in an Irish patientF Daraio, E Ryan, F Gleeson, et al.
Acta Haematologica|October 2, 2008
Deferasirox treatment improved the hemoglobin level and decreased transfusion requirements in four patients with the myelodysplastic syndrome and primary myelofibrosisE Messa, D Cilloni, F Messa, et al.
Blood Cells, Molecules & Diseases|January 10, 2002
Linkage to chromosome 1q in Greek families with juvenile hemochromatosisG Papanikolaou, M Politou, A Roetto, et al.
British Journal of Haematology|April 12, 2000
A new mutation (G51C) in the iron-responsive element (IRE) of L-ferritin associated with hyperferritinaemia-cataract syndrome decreases the binding affinity of the mutated IRE for iron-regulatory proteinsC Camaschella, G Zecchina, G Lockitch, et al.
Human Genetics|April 1, 1996
Allelic association of microsatellites of 6p in Italian hemochromatosis patientsC Camaschella, A Roetto, P Gasparini, et al.
Haematologica|June 15, 1999
Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndromeM Cicilano, G Zecchina, A Roetto, et al.
Molecular and Cellular Probes|October 1, 1993
Construction of a genetic map telomeric to HLA-A by microsatellite analysisC Camaschella, A Roetto, G De Sandre, et al.
Blood Cells, Molecules & Diseases|August 22, 2000
Exclusion of ZIRTL as candidate gene of juvenile hemochromatosis and refinement of the critical interval on 1q21A Roetto, F Alberti, F Daraio, et al.
Pageof 4