Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

B Nobili

Showing results (31-40 of 52) with videos related to

Pageof 6
Sort By:
La Pediatria|September 30, 1982
[Bart's hemoglobin in newborn infants of Campania]A Iolascon, B Nobili, L Pinto, et al.
Transfusion Science|December 2, 2000
L1 effects on reactive oxygen (ROS) and nitrogen species (RNS) release, hemoglobin oxidation, low molecular weight antioxidants, and antioxidant enzyme activities in red and white blood cells of thalassemic patientsL Korkina, C De Luca, I Deeva, et al.
Haematologica|September 1, 1994
Molecular heterogeneity of hereditary elliptocytosis in ItalyE Miraglia del Giudice, S Perrotta, E Sannino, et al.
British Journal of Haematology|February 13, 2001
Clinical and molecular evaluation of non-dominant hereditary spherocytosisE Miraglia del Giudice, B Nobili, M Francese, et al.
The Journal of Pediatrics|January 1, 1997
A trial of high-dose dexamethasone therapy for chronic idiopathic thrombocytopenic purpura in childhoodC Borgna-Pignatti, S Rugolotto, B Nobili, et al.
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 Cardiovascular Pharmacology|November 15, 2001
Effects of nebivolol on human platelet aggregationM Falciani, B Rinaldi, B D'Agostino, et al.
The Journal of Pediatrics|February 7, 2001
Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II)S Perrotta, E M del Giudice, R Carbone, et al.
The Journal of Pediatrics|February 21, 1998
High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosisE Miraglia del Giudice, M Francese, B Nobili, et al.
Bone Marrow Transplantation|April 1, 2003
Successful T-cell-depleted, related haploidentical peripheral blood stem cell transplantation in a patient with Fanconi anaemia using a fludarabine-based preparative regimen without radiationG Rossi, G Giorgiani, P Comoli, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
La Pediatria|September 30, 1982
[Bart's hemoglobin in newborn infants of Campania]A Iolascon, B Nobili, L Pinto, et al.
Transfusion Science|December 2, 2000
L1 effects on reactive oxygen (ROS) and nitrogen species (RNS) release, hemoglobin oxidation, low molecular weight antioxidants, and antioxidant enzyme activities in red and white blood cells of thalassemic patientsL Korkina, C De Luca, I Deeva, et al.
Haematologica|September 1, 1994
Molecular heterogeneity of hereditary elliptocytosis in ItalyE Miraglia del Giudice, S Perrotta, E Sannino, et al.
British Journal of Haematology|February 13, 2001
Clinical and molecular evaluation of non-dominant hereditary spherocytosisE Miraglia del Giudice, B Nobili, M Francese, et al.
The Journal of Pediatrics|January 1, 1997
A trial of high-dose dexamethasone therapy for chronic idiopathic thrombocytopenic purpura in childhoodC Borgna-Pignatti, S Rugolotto, B Nobili, et al.
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 Cardiovascular Pharmacology|November 15, 2001
Effects of nebivolol on human platelet aggregationM Falciani, B Rinaldi, B D'Agostino, et al.
The Journal of Pediatrics|February 7, 2001
Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II)S Perrotta, E M del Giudice, R Carbone, et al.
The Journal of Pediatrics|February 21, 1998
High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosisE Miraglia del Giudice, M Francese, B Nobili, et al.
Bone Marrow Transplantation|April 1, 2003
Successful T-cell-depleted, related haploidentical peripheral blood stem cell transplantation in a patient with Fanconi anaemia using a fludarabine-based preparative regimen without radiationG Rossi, G Giorgiani, P Comoli, et al.
Pageof 6