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

A Iolascon

Showing results (61-70 of 154) with videos related to

Pageof 16
Sort By:
La Pediatria|June 1, 1983
[Sanfilippo's disease of type B. Study of the enzymatic deficiency in a family]B Nobili, A Iolascon, L Bello, 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.
British Journal of Haematology|November 1, 1993
Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotypeE Miraglia del Giudice, S Perrotta, B Nobili, et al.
Haematologica|September 8, 1999
Genetic heterogeneity of hereditary stomatocytosis syndromes showing pseudohyperkalemiaM Carella, G W Stewart, J F Ajetunmobi, et al.
Haematologica|May 9, 1998
Hereditary spherocytosis: from clinical to molecular defectsA Iolascon, E Miraglia del Giudice, S Perrotta, et al.
Blood|November 14, 1997
Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II)A Iolascon, E Miraglia del Giudice, S Perrotta, et al.
Minerva Pediatrica|October 20, 2007
[New types of microcytic anemia]A Iolascon, L De Falco, L Boschetto, et al.
Blood|September 25, 1998
Genetic heterogeneity of congenital dyserythropoietic anemia type IIA Iolascon, D De Mattia, S Perrotta, et al.
Haematologica|July 16, 1999
4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosisS Perrotta, A Iolascon, R Polito, et al.
Genes, Chromosomes & Cancer|September 1, 1996
Peculiar allelotype associated with susceptibility to neuroblastomaP Perri, A Pession, K Mazzocco, et al.
Pageof 16

Showing results (61-70 of 154) with videos related to

Sort By:
Pageof 16
La Pediatria|June 1, 1983
[Sanfilippo's disease of type B. Study of the enzymatic deficiency in a family]B Nobili, A Iolascon, L Bello, 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.
British Journal of Haematology|November 1, 1993
Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta-thalassaemia trait: partial correction of HS phenotypeE Miraglia del Giudice, S Perrotta, B Nobili, et al.
Haematologica|September 8, 1999
Genetic heterogeneity of hereditary stomatocytosis syndromes showing pseudohyperkalemiaM Carella, G W Stewart, J F Ajetunmobi, et al.
Haematologica|May 9, 1998
Hereditary spherocytosis: from clinical to molecular defectsA Iolascon, E Miraglia del Giudice, S Perrotta, et al.
Blood|November 14, 1997
Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II)A Iolascon, E Miraglia del Giudice, S Perrotta, et al.
Minerva Pediatrica|October 20, 2007
[New types of microcytic anemia]A Iolascon, L De Falco, L Boschetto, et al.
Blood|September 25, 1998
Genetic heterogeneity of congenital dyserythropoietic anemia type IIA Iolascon, D De Mattia, S Perrotta, et al.
Haematologica|July 16, 1999
4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosisS Perrotta, A Iolascon, R Polito, et al.
Genes, Chromosomes & Cancer|September 1, 1996
Peculiar allelotype associated with susceptibility to neuroblastomaP Perri, A Pession, K Mazzocco, et al.
Pageof 16