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

Lea M Coon

Showing results (1-10 of 13) with videos related to

Pageof 2
Sort By:
Seminars in Thrombosis and Hemostasis|January 11, 2019
Factor V Deficiency with a Thrombotic Clinical PhenotypeMeera Sridharan, Lea M Coon, Dong Chen, et al.
Seminars in Thrombosis and Hemostasis|September 15, 2017
Factor IX Gene (F9) Genotyping Trends and Spectrum of Mutations Identified: A Reference Laboratory ExperienceJuliana Perez Botero, Lea M Coon, Julie A Majerus, et al.
Acta Haematologica|February 21, 2019
Case Report: Development of Factor VIII Inhibitor in a Patient with an Uncommon de novo Mutation in the Factor VIII GeneKirk D Wyatt, Lea M Coon, Dawn N Rusk, et al.
Hypoxia (Auckland, N.Z.)|December 20, 2019
An Erythrocytosis-Associated Mutation in the Zinc Finger of PHD2 Provides Insights into Its Binding of p23Daisheng Song, Wei Guan, Lea M Coon, et al.
JACC. Case Reports|December 12, 2025
Autosomal-Recessive LMNA Dilated CardiomyopathyRosalie M Sterner, Lea M Coon, John L Black, et al.
Hemoglobin|December 19, 2015
A Novel β-Globin Chain Hemoglobin Variant, Hb Allentown [β137(H15)Val→Trp (GTG>TGG) HBB: c.412_413delinsTG, p.Val138Trp], Associated with Low Oxygen Saturation, Intermittent Aplastic Crises and SplenomegalyAnderson B Collier, Lea M Coon, Philip Monteleone, et al.
Journal of Pediatric Hematology/Oncology|June 5, 2020
Hereditary Thrombotic Thrombocytopenic Purpura in a 9-Month-old: Diagnosing and Managing an Ultra-rare DisorderKirk D Wyatt, Mira A Kohorst, Lea M Coon, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 9, 2016
Practice patterns in the diagnosis of inherited platelet disorders within a single institutionJuliana Perez Botero, Rajiv K Pruthi, Julie A Majerus, et al.
Platelets|November 2, 2017
Hermansky-Pudlak syndrome subtype 5 (HPS-5) novel mutation in a 65 year-old with oculocutaneous hypopigmentation and mild bleeding diathesis: The importance of recognizing a subtle phenotypeJuliana Perez Botero, Dong Chen, Julie A Majerus, et al.
Leukemia & Lymphoma|December 10, 2016
Clinical characteristics and platelet phenotype in a family with RUNX1 mutated thrombocytopeniaJuliana Perez Botero, Dong Chen, Margot A Cousin, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Seminars in Thrombosis and Hemostasis|January 11, 2019
Factor V Deficiency with a Thrombotic Clinical PhenotypeMeera Sridharan, Lea M Coon, Dong Chen, et al.
Seminars in Thrombosis and Hemostasis|September 15, 2017
Factor IX Gene (F9) Genotyping Trends and Spectrum of Mutations Identified: A Reference Laboratory ExperienceJuliana Perez Botero, Lea M Coon, Julie A Majerus, et al.
Acta Haematologica|February 21, 2019
Case Report: Development of Factor VIII Inhibitor in a Patient with an Uncommon de novo Mutation in the Factor VIII GeneKirk D Wyatt, Lea M Coon, Dawn N Rusk, et al.
Hypoxia (Auckland, N.Z.)|December 20, 2019
An Erythrocytosis-Associated Mutation in the Zinc Finger of PHD2 Provides Insights into Its Binding of p23Daisheng Song, Wei Guan, Lea M Coon, et al.
JACC. Case Reports|December 12, 2025
Autosomal-Recessive LMNA Dilated CardiomyopathyRosalie M Sterner, Lea M Coon, John L Black, et al.
Hemoglobin|December 19, 2015
A Novel β-Globin Chain Hemoglobin Variant, Hb Allentown [β137(H15)Val→Trp (GTG>TGG) HBB: c.412_413delinsTG, p.Val138Trp], Associated with Low Oxygen Saturation, Intermittent Aplastic Crises and SplenomegalyAnderson B Collier, Lea M Coon, Philip Monteleone, et al.
Journal of Pediatric Hematology/Oncology|June 5, 2020
Hereditary Thrombotic Thrombocytopenic Purpura in a 9-Month-old: Diagnosing and Managing an Ultra-rare DisorderKirk D Wyatt, Mira A Kohorst, Lea M Coon, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 9, 2016
Practice patterns in the diagnosis of inherited platelet disorders within a single institutionJuliana Perez Botero, Rajiv K Pruthi, Julie A Majerus, et al.
Platelets|November 2, 2017
Hermansky-Pudlak syndrome subtype 5 (HPS-5) novel mutation in a 65 year-old with oculocutaneous hypopigmentation and mild bleeding diathesis: The importance of recognizing a subtle phenotypeJuliana Perez Botero, Dong Chen, Julie A Majerus, et al.
Leukemia & Lymphoma|December 10, 2016
Clinical characteristics and platelet phenotype in a family with RUNX1 mutated thrombocytopeniaJuliana Perez Botero, Dong Chen, Margot A Cousin, et al.
Pageof 2