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

M Kalafatis

Showing results (51-60 of 54) with videos related to

Pageof 6
Sort By:
You have reached the last page of results.This site can display upto 54 results.
Blood|September 15, 1996
Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasmaP Simioni, M Kalafatis, D S Millar, et al.
Blood|May 1, 1986
Mapping of distinct von Willebrand factor domains interacting with platelet GPIb and GPIIb/IIIa and with collagen using monoclonal antibodiesJ P Girma, M Kalafatis, G Piétu, et al.
Thrombosis and Haemostasis|October 6, 1998
Molecular bases of pseudo-homozygous APC resistance: the compound heterozygosity for FV R506Q and a FV null mutation results in the exclusive presence of FV Leiden molecules in plasmaE Castoldi, M Kalafatis, B Lunghi, et al.
Thrombosis Research|March 15, 2001
A dysfunctional factor X (factor X San Giovanni Rotondo) present at homozygous and double heterozygous level: identification of a novel microdeletion (delC556) and missense mutation (Lys(408)-->Asn) in the factor X gene. A study of an Italian familyP Simioni, F Vianello, M Kalafatis, et al.
Pageof 6

Showing results (51-60 of 54) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 54 results.
Blood|September 15, 1996
Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasmaP Simioni, M Kalafatis, D S Millar, et al.
Blood|May 1, 1986
Mapping of distinct von Willebrand factor domains interacting with platelet GPIb and GPIIb/IIIa and with collagen using monoclonal antibodiesJ P Girma, M Kalafatis, G Piétu, et al.
Thrombosis and Haemostasis|October 6, 1998
Molecular bases of pseudo-homozygous APC resistance: the compound heterozygosity for FV R506Q and a FV null mutation results in the exclusive presence of FV Leiden molecules in plasmaE Castoldi, M Kalafatis, B Lunghi, et al.
Thrombosis Research|March 15, 2001
A dysfunctional factor X (factor X San Giovanni Rotondo) present at homozygous and double heterozygous level: identification of a novel microdeletion (delC556) and missense mutation (Lys(408)-->Asn) in the factor X gene. A study of an Italian familyP Simioni, F Vianello, M Kalafatis, et al.
Pageof 6