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A Iolascon

Showing results (21-30 of 154) with videos related to

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Journal of Medical Genetics|February 24, 2001
Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) geneA Iolascon, A Meloni, B Coppola, et al.
Acta Haematologica|October 26, 1999
Homozygous prothrombin gene mutation and ischemic cerebrovascular disease: a case reportP Giordano, D De Lucia, B Coppola, et al.
Bone Marrow Transplantation|April 3, 2001
Bone marrow transplantation in a case of severe, type II congenital dyserythropoietic anaemia (CDA II)A Iolascon, V Sabato, D de Mattia, et al.
La Pediatria|October 1, 1983
[Current possibilities of the use of ferritin in clinical diagnosis]M Galdo Capotorti, G Mascolo, B Nobili, et al.
La Pediatria|June 30, 1979
[Fluorimetric determination of erythrocytic free protoporphyrins in evaluation of iron deficiency states]L Pinto, B Nobili, R Vitale, et al.
Annali Dell'Istituto Superiore Di Sanita|July 29, 1998
[Blood lead levels during pregnancy in th the newborn period. Study of the population of Bari]R Carbone, N Laforgia, E Crollo, et al.
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.
Human Mutation|May 2, 2000
Characterization of the CYP21 gene 5' flanking region in patients affected by 21-OH deficiencyA Bobba, E Marra, P Lattanzio, 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|November 1, 1988
Analysis of gamma globin chain composition in childhood acute lymphocytic leukemia (ALL)A Iolascon, L Pinto, M T Di Tullio, et al.
Pageof 16

Showing results (21-30 of 154) with videos related to

Sort By:
Pageof 16
Journal of Medical Genetics|February 24, 2001
Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) geneA Iolascon, A Meloni, B Coppola, et al.
Acta Haematologica|October 26, 1999
Homozygous prothrombin gene mutation and ischemic cerebrovascular disease: a case reportP Giordano, D De Lucia, B Coppola, et al.
Bone Marrow Transplantation|April 3, 2001
Bone marrow transplantation in a case of severe, type II congenital dyserythropoietic anaemia (CDA II)A Iolascon, V Sabato, D de Mattia, et al.
La Pediatria|October 1, 1983
[Current possibilities of the use of ferritin in clinical diagnosis]M Galdo Capotorti, G Mascolo, B Nobili, et al.
La Pediatria|June 30, 1979
[Fluorimetric determination of erythrocytic free protoporphyrins in evaluation of iron deficiency states]L Pinto, B Nobili, R Vitale, et al.
Annali Dell'Istituto Superiore Di Sanita|July 29, 1998
[Blood lead levels during pregnancy in th the newborn period. Study of the population of Bari]R Carbone, N Laforgia, E Crollo, et al.
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.
Human Mutation|May 2, 2000
Characterization of the CYP21 gene 5' flanking region in patients affected by 21-OH deficiencyA Bobba, E Marra, P Lattanzio, 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|November 1, 1988
Analysis of gamma globin chain composition in childhood acute lymphocytic leukemia (ALL)A Iolascon, L Pinto, M T Di Tullio, et al.
Pageof 16