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A Iolascon

Showing results (41-50 of 154) with videos related to

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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.
Acta Paediatrica (Oslo, Norway : 1992)|November 14, 1997
Rapid detection of neonatal sepsis using polymerase chain reactionN Laforgia, B Coppola, R Carbone, 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.
European Journal of Pediatrics|January 1, 1992
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosisS Cutillo, L Pinto, B Nobili, et al.
International Journal of Clinical & Laboratory Research|April 28, 2000
Analysis of three genetic polymorphisms as risk factors for thrombosisP Giordano, M Micelli, B Coppola, et al.
Haematologica|March 26, 1999
(TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndromeA Iolascon, M F Faienza, M Centra, et al.
Blood|August 9, 2001
Natural history of congenital dyserythropoietic anemia type IIA Iolascon, J Delaunay, S N Wickramasinghe, 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.
Journal of Perinatal Medicine|May 10, 2001
Renal vein thrombosis in a newborn with prothrombotic genetic risk factorsP Giordano, N Laforgia, G Di Giulio, et al.
Human Genetics|January 1, 1985
Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in southern Italy: a study on the population of NaplesS Colonna-Romano, A Iolascon, S Lippo, et al.
Pageof 16

Showing results (41-50 of 154) with videos related to

Sort By:
Pageof 16
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.
Acta Paediatrica (Oslo, Norway : 1992)|November 14, 1997
Rapid detection of neonatal sepsis using polymerase chain reactionN Laforgia, B Coppola, R Carbone, 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.
European Journal of Pediatrics|January 1, 1992
Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosisS Cutillo, L Pinto, B Nobili, et al.
International Journal of Clinical & Laboratory Research|April 28, 2000
Analysis of three genetic polymorphisms as risk factors for thrombosisP Giordano, M Micelli, B Coppola, et al.
Haematologica|March 26, 1999
(TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndromeA Iolascon, M F Faienza, M Centra, et al.
Blood|August 9, 2001
Natural history of congenital dyserythropoietic anemia type IIA Iolascon, J Delaunay, S N Wickramasinghe, 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.
Journal of Perinatal Medicine|May 10, 2001
Renal vein thrombosis in a newborn with prothrombotic genetic risk factorsP Giordano, N Laforgia, G Di Giulio, et al.
Human Genetics|January 1, 1985
Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in southern Italy: a study on the population of NaplesS Colonna-Romano, A Iolascon, S Lippo, et al.
Pageof 16