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

Maria Lombardi

Showing results (41-50 of 108) with videos related to

Pageof 11
Sort By:
Scientific Reports|September 16, 2021
Spontaneous emergence of leadership patterns drives synchronization in complex human networksCarmela Calabrese, Maria Lombardi, Erik Bollt, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|February 26, 2004
A large deletion due to a new mutation (intron 13/exon 23) in a sporadic case of severe hemophilia AAnna Maria Lombardi, Laura Cabrio, Ezio Zanon, et al.
Haematologica|September 26, 2008
Novel point mutation in a leucine-rich repeat of the GPIbalpha chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variantSilvia Vettore, Raffaella Scandellari, Stefano Moro, et al.
Platelets|September 16, 2008
A case of Bernard-Soulier Syndrome due to a homozygous four bases deletion (TGAG) of GPIbalpha gene: lack of GPIbalpha but absence of bleedingSilvia Vettore, Raffaella Scandellari, Margherita Scapin, et al.
Annals of Hematology|June 7, 2017
Thromboses and hemorrhages are common in MPN patients with high JAK2V617F allele burdenIrene Bertozzi, Giulia Bogoni, Giacomo Biagetti, et al.
Anticancer Research|June 25, 2003
p53 polymorphism at codon 72 is not a risk factor for cervical carcinogenesis in central ItalyMaria Cenci, Deborah French, Tiziana Pisani, et al.
Hematology Reports|April 19, 2019
Relapsing thrombotic thrombocytopenic purpura with low ADAMTS13 antigen levels: An indication for splenectomy?Anna Maria Lombardi, Irene Di Pasquale, Maria Antonietta Businaro, et al.
International Journal of Cardiology|December 26, 2018
IL-1β/MMP9 activation in primary human vascular smooth muscle-like cells: Exploring the role of TNFα and P2X7Maria Elena Mantione, Maria Lombardi, Domenico Baccellieri, et al.
Scientific Reports|July 9, 2017
P2X7 receptor antagonism modulates IL-1β and MMP9 in human atherosclerotic vesselsMaria Lombardi, Maria Elena Mantione, Domenico Baccellieri, et al.
International Journal of Molecular Sciences|April 30, 2021
Confocal Blood Flow Videomicroscopy of Thrombus Formation over Human Arteries and Local Targeting of P2X7Patrizia Marchese, Maria Lombardi, Maria Elena Mantione, et al.
Pageof 11

Showing results (41-50 of 108) with videos related to

Sort By:
Pageof 11
Scientific Reports|September 16, 2021
Spontaneous emergence of leadership patterns drives synchronization in complex human networksCarmela Calabrese, Maria Lombardi, Erik Bollt, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|February 26, 2004
A large deletion due to a new mutation (intron 13/exon 23) in a sporadic case of severe hemophilia AAnna Maria Lombardi, Laura Cabrio, Ezio Zanon, et al.
Haematologica|September 26, 2008
Novel point mutation in a leucine-rich repeat of the GPIbalpha chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variantSilvia Vettore, Raffaella Scandellari, Stefano Moro, et al.
Platelets|September 16, 2008
A case of Bernard-Soulier Syndrome due to a homozygous four bases deletion (TGAG) of GPIbalpha gene: lack of GPIbalpha but absence of bleedingSilvia Vettore, Raffaella Scandellari, Margherita Scapin, et al.
Annals of Hematology|June 7, 2017
Thromboses and hemorrhages are common in MPN patients with high JAK2V617F allele burdenIrene Bertozzi, Giulia Bogoni, Giacomo Biagetti, et al.
Anticancer Research|June 25, 2003
p53 polymorphism at codon 72 is not a risk factor for cervical carcinogenesis in central ItalyMaria Cenci, Deborah French, Tiziana Pisani, et al.
Hematology Reports|April 19, 2019
Relapsing thrombotic thrombocytopenic purpura with low ADAMTS13 antigen levels: An indication for splenectomy?Anna Maria Lombardi, Irene Di Pasquale, Maria Antonietta Businaro, et al.
International Journal of Cardiology|December 26, 2018
IL-1β/MMP9 activation in primary human vascular smooth muscle-like cells: Exploring the role of TNFα and P2X7Maria Elena Mantione, Maria Lombardi, Domenico Baccellieri, et al.
Scientific Reports|July 9, 2017
P2X7 receptor antagonism modulates IL-1β and MMP9 in human atherosclerotic vesselsMaria Lombardi, Maria Elena Mantione, Domenico Baccellieri, et al.
International Journal of Molecular Sciences|April 30, 2021
Confocal Blood Flow Videomicroscopy of Thrombus Formation over Human Arteries and Local Targeting of P2X7Patrizia Marchese, Maria Lombardi, Maria Elena Mantione, et al.
Pageof 11