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E Miraglia del Giudice

Showing results (1-10 of 74) with videos related to

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Haematologica|January 1, 1992
Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosisA Iolascon, E Miraglia del Giudice, C Camaschella
Haematologica|May 21, 1998
Decision making at the bedside: diagnosis of hereditary spherocytosis in a transfused infantE Miraglia del Giudice, S Perrotta, C Lombardi, et al.
British Journal of Haematology|September 1, 1994
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosisE Miraglia del Giudice, A Iolascon, L Pinto, et al.
European Journal of Pediatrics|January 1, 1992
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosisS Cutillo, L Pinto, B Nobili, et al.
Acta Haematologica|January 1, 1995
Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian childS Gangarossa, V Romano, E Miraglia del Giudice, et al.
Haematologica|May 1, 1997
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) alleleE Miraglia del Giudice, M Francese, R Polito, et al.
British Journal of Haematology|November 1, 1993
Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotypeE Miraglia del Giudice, S Perrotta, B Nobili, et al.
Haematologica|May 9, 1998
Hereditary spherocytosis: from clinical to molecular defectsA Iolascon, E Miraglia del Giudice, S Perrotta, et al.
Blood|November 14, 1997
Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II)A Iolascon, E Miraglia del Giudice, S Perrotta, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Benign familial neonatal convulsions (BFNC) resulting from mutation of the KCNQ2 voltage sensorE Miraglia del Giudice, G Coppola, G Scuccimarra, et al.
Pageof 8

Showing results (1-10 of 74) with videos related to

Sort By:
Pageof 8
Haematologica|January 1, 1992
Molecular pathology of inherited erythrocyte membrane disorders: hereditary spherocytosis and elliptocytosisA Iolascon, E Miraglia del Giudice, C Camaschella
Haematologica|May 21, 1998
Decision making at the bedside: diagnosis of hereditary spherocytosis in a transfused infantE Miraglia del Giudice, S Perrotta, C Lombardi, et al.
British Journal of Haematology|September 1, 1994
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosisE Miraglia del Giudice, A Iolascon, L Pinto, et al.
European Journal of Pediatrics|January 1, 1992
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosisS Cutillo, L Pinto, B Nobili, et al.
Acta Haematologica|January 1, 1995
Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian childS Gangarossa, V Romano, E Miraglia del Giudice, et al.
Haematologica|May 1, 1997
Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) alleleE Miraglia del Giudice, M Francese, R Polito, et al.
British Journal of Haematology|November 1, 1993
Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotypeE Miraglia del Giudice, S Perrotta, B Nobili, et al.
Haematologica|May 9, 1998
Hereditary spherocytosis: from clinical to molecular defectsA Iolascon, E Miraglia del Giudice, S Perrotta, et al.
Blood|November 14, 1997
Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II)A Iolascon, E Miraglia del Giudice, S Perrotta, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Benign familial neonatal convulsions (BFNC) resulting from mutation of the KCNQ2 voltage sensorE Miraglia del Giudice, G Coppola, G Scuccimarra, et al.
Pageof 8