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E Miraglia Del Giudice

Showing results (1-10 of 89) 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.
Acta Haematologica|January 1, 1989
A modification of the 'pink test' may improve the diagnosis of hereditary spherocytosisL Pinto, A Iolascon, E Miraglia del Giudice, et al.
Haematologica|March 7, 2000
Frequency of Gilbert's syndrome associated with UGTA1 (TA)(7) polymorphism in Southern ItalyA Iolascon, S Perrotta, B Coppola, 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, 1993
A rapid method for the detection of alpha I/65 hereditary elliptocytosisA Iolascon, E Miraglia del Giudice, S Perrotta, et al.
Blood|February 3, 1998
UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosisA Iolascon, M F Faienza, A Moretti, 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.
Pageof 9

Showing results (1-10 of 89) with videos related to

Sort By:
Pageof 9
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.
Acta Haematologica|January 1, 1989
A modification of the 'pink test' may improve the diagnosis of hereditary spherocytosisL Pinto, A Iolascon, E Miraglia del Giudice, et al.
Haematologica|March 7, 2000
Frequency of Gilbert's syndrome associated with UGTA1 (TA)(7) polymorphism in Southern ItalyA Iolascon, S Perrotta, B Coppola, 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, 1993
A rapid method for the detection of alpha I/65 hereditary elliptocytosisA Iolascon, E Miraglia del Giudice, S Perrotta, et al.
Blood|February 3, 1998
UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosisA Iolascon, M F Faienza, A Moretti, 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.
Pageof 9