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

Silverio Perrotta

Showing results (61-70 of 200) with videos related to

Pageof 20
Sort By:
British Journal of Haematology|September 12, 2008
Erythropoietin treatment can prevent blood transfusion in infantile pyknocytosisGiovanni Amendola, Rosanna Di Concilio, Giovanna D'Urzo, et al.
FEBS Letters|November 23, 2006
Characterization of red cell membrane proteins as a function of red cell density: annexin VII in different forms of hereditary spherocytosisMarianna Caterino, Margherita Ruoppolo, Stefania Orrù, et al.
Blood Cells, Molecules & Diseases|April 2, 2003
Congenital dyserythropoietic anemia type II: exclusion of seven candidate genesCarmela Lanzara, Romina Ficarella, Angela Totaro, et al.
European Journal of Medical Genetics|March 16, 2021
A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndromeClaudia Santoro, Simona Riccio, Federica Palladino, et al.
Journal of Nephrology|May 30, 2012
HNF-1β mutation affects PKD2 and SOCS3 expression causing renal cysts and diabetes in MODY5 kindredSilvia Mancusi, Angela La Manna, Giulia Bellini, et al.
Haematologica|December 18, 2009
Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationshipAchille Iolascon, Roberta Russo, Maria Rosaria Esposito, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 2, 2003
Inappropriate leptin secretion in thalassemia: a potential cofactor of pubertal timing derangementLaura Perrone, Silverio Perrotta, Paolo Raimondo, et al.
International Journal of Molecular Sciences|December 30, 2020
Effects of Eltrombopag on In Vitro Macrophage Polarization in Pediatric Immune ThrombocytopeniaAlessandra Di Paola, Giuseppe Palumbo, Pietro Merli, et al.
Molecular Oncology|December 14, 2020
A cancer-associated CDKN1B mutation induces p27 phosphorylation on a novel residue: a new mechanism for tumor suppressor loss-of-functionDebora Bencivenga, Emanuela Stampone, Arianna Aulitto, et al.
BMC Medical Genetics|April 29, 2014
LEOPARD syndrome: clinical dilemmas in differential diagnosis of RASopathiesClaudia Santoro, Giuseppe Pacileo, Giuseppe Limongelli, et al.
Pageof 20

Showing results (61-70 of 200) with videos related to

Sort By:
Pageof 20
British Journal of Haematology|September 12, 2008
Erythropoietin treatment can prevent blood transfusion in infantile pyknocytosisGiovanni Amendola, Rosanna Di Concilio, Giovanna D'Urzo, et al.
FEBS Letters|November 23, 2006
Characterization of red cell membrane proteins as a function of red cell density: annexin VII in different forms of hereditary spherocytosisMarianna Caterino, Margherita Ruoppolo, Stefania Orrù, et al.
Blood Cells, Molecules & Diseases|April 2, 2003
Congenital dyserythropoietic anemia type II: exclusion of seven candidate genesCarmela Lanzara, Romina Ficarella, Angela Totaro, et al.
European Journal of Medical Genetics|March 16, 2021
A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndromeClaudia Santoro, Simona Riccio, Federica Palladino, et al.
Journal of Nephrology|May 30, 2012
HNF-1β mutation affects PKD2 and SOCS3 expression causing renal cysts and diabetes in MODY5 kindredSilvia Mancusi, Angela La Manna, Giulia Bellini, et al.
Haematologica|December 18, 2009
Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationshipAchille Iolascon, Roberta Russo, Maria Rosaria Esposito, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 2, 2003
Inappropriate leptin secretion in thalassemia: a potential cofactor of pubertal timing derangementLaura Perrone, Silverio Perrotta, Paolo Raimondo, et al.
International Journal of Molecular Sciences|December 30, 2020
Effects of Eltrombopag on In Vitro Macrophage Polarization in Pediatric Immune ThrombocytopeniaAlessandra Di Paola, Giuseppe Palumbo, Pietro Merli, et al.
Molecular Oncology|December 14, 2020
A cancer-associated CDKN1B mutation induces p27 phosphorylation on a novel residue: a new mechanism for tumor suppressor loss-of-functionDebora Bencivenga, Emanuela Stampone, Arianna Aulitto, et al.
BMC Medical Genetics|April 29, 2014
LEOPARD syndrome: clinical dilemmas in differential diagnosis of RASopathiesClaudia Santoro, Giuseppe Pacileo, Giuseppe Limongelli, et al.
Pageof 20