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A Iolascon

Showing results (141-150 of 154) with videos related to

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European Journal of Cancer (Oxford, England : 1990)|March 28, 1998
Loss of heterozygosity for chromosome 1p in familial neuroblastomaG P Tonini, C Lo Cunsolo, R Cusano, et al.
Cancer Genetics and Cytogenetics|March 24, 1999
Neuroblastoma in two siblings supports the role of 1p36 deletion in tumor developmentC Lo Cunsolo, A Iolascon, A Cavazzana, et al.
The Journal of Biological Chemistry|October 25, 1993
Spectrin cagliari. an Ala-->Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimerK E Sahr, T L Coetzer, L S Moy, et al.
Haematologica|January 12, 2000
Heavy transfusions and presence of an anti-protein 4.2 antibody in 4. 2(-) hereditary spherocytosis (949delG)A Beauchamp-Nicoud, L Morle, H U Lutz, et al.
Cancer Letters|September 29, 1998
Interstitial and large chromosome 1p deletion occurs in localized and disseminated neuroblastomas and predicts an unfavourable outcomeA Iolascon, C Lo Cunsolo, L Giordani, et al.
Haematologica|October 17, 2001
Thrombophilia in thalassemia major patients: analysis of genetic predisposing factorsA Iolascon, P Giordano, S Storelli, et al.
British Journal of Haematology|November 25, 1998
Mutational screening of thrombopoietin receptor gene (c-mpl) in patients with congenital thrombocytopenia and absent radii (TAR)P Strippoli, A Savoia, A Iolascon, et al.
British Journal of Haematology|October 16, 1999
Suppression of CDA II expression in a homozygoteA Beauchamp-Nicoud, P O Schischmanoff, N Alloisio, et al.
Thrombosis and Haemostasis|July 15, 2000
Hereditary thrombocytopenia due to reduced platelet production--report on two families and mutational screening of the thrombopoietin receptor gene (c-mpl)R Tonelli, P Strippoli, A Grossi, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosisG Tchernia, F Delhommeau, S Perrotta, et al.
Pageof 16

Showing results (141-150 of 154) with videos related to

Sort By:
Pageof 16
European Journal of Cancer (Oxford, England : 1990)|March 28, 1998
Loss of heterozygosity for chromosome 1p in familial neuroblastomaG P Tonini, C Lo Cunsolo, R Cusano, et al.
Cancer Genetics and Cytogenetics|March 24, 1999
Neuroblastoma in two siblings supports the role of 1p36 deletion in tumor developmentC Lo Cunsolo, A Iolascon, A Cavazzana, et al.
The Journal of Biological Chemistry|October 25, 1993
Spectrin cagliari. an Ala-->Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimerK E Sahr, T L Coetzer, L S Moy, et al.
Haematologica|January 12, 2000
Heavy transfusions and presence of an anti-protein 4.2 antibody in 4. 2(-) hereditary spherocytosis (949delG)A Beauchamp-Nicoud, L Morle, H U Lutz, et al.
Cancer Letters|September 29, 1998
Interstitial and large chromosome 1p deletion occurs in localized and disseminated neuroblastomas and predicts an unfavourable outcomeA Iolascon, C Lo Cunsolo, L Giordani, et al.
Haematologica|October 17, 2001
Thrombophilia in thalassemia major patients: analysis of genetic predisposing factorsA Iolascon, P Giordano, S Storelli, et al.
British Journal of Haematology|November 25, 1998
Mutational screening of thrombopoietin receptor gene (c-mpl) in patients with congenital thrombocytopenia and absent radii (TAR)P Strippoli, A Savoia, A Iolascon, et al.
British Journal of Haematology|October 16, 1999
Suppression of CDA II expression in a homozygoteA Beauchamp-Nicoud, P O Schischmanoff, N Alloisio, et al.
Thrombosis and Haemostasis|July 15, 2000
Hereditary thrombocytopenia due to reduced platelet production--report on two families and mutational screening of the thrombopoietin receptor gene (c-mpl)R Tonelli, P Strippoli, A Grossi, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosisG Tchernia, F Delhommeau, S Perrotta, et al.
Pageof 16