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A Iolascon

Showing results (81-90 of 154) with videos related to

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British Journal of Haematology|August 1, 1991
Ankyrin deficiency in dominant hereditary spherocytosis: report of three casesA Iolascon, E Miraglia del Giudice, C Camaschella, et al.
Journal of Medical Genetics|July 1, 1994
Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigelsA Iolascon, T Parrella, S Perrotta, et al.
American Journal of Hematology|July 1, 1997
Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defectsL De Franceschi, O Olivieri, E Miraglia del Giudice, et al.
Pediatric Research|December 14, 1999
Familial dominant thrombocytopenia: clinical, biologic, and molecular studiesA Iolascon, S Perrotta, G Amendola, et al.
Oncogene|April 14, 2009
Galectin-1 is a major effector of TrkB-mediated neuroblastoma aggressivenessF Cimmino, J H Schulte, M Zollo, et al.
European Journal of Haematology|August 26, 1998
Resistance to activated protein C in thalassaemic patients: an underlying cause of thrombosisP Giordano, G C Del Vecchio, M Altomare, et al.
American Journal of Human Genetics|October 16, 1999
An autosomal dominant thrombocytopenia gene maps to chromosomal region 10pA Savoia, M Del Vecchio, A Totaro, et al.
British Journal of Haematology|April 1, 1995
Spectrin Anastasia (alpha I/78): a new spectrin variant (alpha 45 Arg-->Thr) with moderate elliptocytogenic potentialS Perrotta, A Iolascon, F De Angelis, et al.
Blood|April 3, 1999
Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail: band 3 VesuvioS Perrotta, F Polito, M L Cone, et al.
British Journal of Haematology|October 1, 1994
A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin NapoliR Wilmotte, E Miraglia del Giudice, J Marechal, et al.
Pageof 16

Showing results (81-90 of 154) with videos related to

Sort By:
Pageof 16
British Journal of Haematology|August 1, 1991
Ankyrin deficiency in dominant hereditary spherocytosis: report of three casesA Iolascon, E Miraglia del Giudice, C Camaschella, et al.
Journal of Medical Genetics|July 1, 1994
Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigelsA Iolascon, T Parrella, S Perrotta, et al.
American Journal of Hematology|July 1, 1997
Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defectsL De Franceschi, O Olivieri, E Miraglia del Giudice, et al.
Pediatric Research|December 14, 1999
Familial dominant thrombocytopenia: clinical, biologic, and molecular studiesA Iolascon, S Perrotta, G Amendola, et al.
Oncogene|April 14, 2009
Galectin-1 is a major effector of TrkB-mediated neuroblastoma aggressivenessF Cimmino, J H Schulte, M Zollo, et al.
European Journal of Haematology|August 26, 1998
Resistance to activated protein C in thalassaemic patients: an underlying cause of thrombosisP Giordano, G C Del Vecchio, M Altomare, et al.
American Journal of Human Genetics|October 16, 1999
An autosomal dominant thrombocytopenia gene maps to chromosomal region 10pA Savoia, M Del Vecchio, A Totaro, et al.
British Journal of Haematology|April 1, 1995
Spectrin Anastasia (alpha I/78): a new spectrin variant (alpha 45 Arg-->Thr) with moderate elliptocytogenic potentialS Perrotta, A Iolascon, F De Angelis, et al.
Blood|April 3, 1999
Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail: band 3 VesuvioS Perrotta, F Polito, M L Cone, et al.
British Journal of Haematology|October 1, 1994
A deletional frameshift mutation in spectrin beta-gene associated with hereditary elliptocytosis in spectrin NapoliR Wilmotte, E Miraglia del Giudice, J Marechal, et al.
Pageof 16