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

Shadi Tabibian

Showing results (21-30 of 58) with videos related to

Pageof 6
Sort By:
Turkish Journal of Medical Sciences|August 12, 2016
Childhood acute lymphoblastic leukemia: refusal and abandonmentof treatment in the southeast of IranMajid Naderi, Samira Esmaeili Reykande, Shadi Tabibian, et al.
Hematology (Amsterdam, Netherlands)|December 30, 2014
Association between expression of MMP-2 and MMP-9 genes and pathogenesis of intracranial hemorrhage in severe coagulation factor XIII deficiencyMajid Naderi, Mohammad Reza Younesi, Akbar Dorgalaleh, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 19, 2016
Spectrum of factor X gene mutations in Iranian patients with congenital factor X deficiencyAkbar Dorgalaleh, Farhad Zaker, Shadi Tabibian, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|March 25, 2021
Congenital Combined Bleeding Disorders, a Comprehensive Study of a Large Number of Iranian PatientsSeyed Esmaeil Ahmadi, Mohammad Jazebi, Gholamreza Bahoush, et al.
Laboratory Medicine|August 14, 2016
Comparison of 2 Methods of Clot Solubility Testing in Detection of Factor XIII DeficiencyAkbar Dorgalaleh, Shadi Tabibian, Vahideh Assadollahi, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 3, 2016
Disseminated intravascular coagulation with positive D-dimer: a controversial clinical feature in severe congenital factor XIII deficiency in southeast IranMajid Naderi, Shadi Tabibian, Marzia Menegatti, et al.
International Journal of Hematology|September 19, 2014
Clinical manifestations and management of life-threatening bleeding in the largest group of patients with severe factor XIII deficiencyMajid Naderi, Akbar Dorgalaleh, Shaban Alizadeh, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|July 12, 2025
Identification of novel RASGRP2 mutations in patients with platelet dysfunctionMohadese Heydarali Broojerdi, Shadi Tabibian, Rima Manafi Shabestari, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|April 13, 2024
Molecular and clinical profile of rare bleeding disorders: A single-center retrospective studyArash Ahmadfard Moghadam, Amir Reza Manafzadeh, Mohammad Reza Nikoonia, et al.
Seminars in Thrombosis and Hemostasis|January 24, 2015
Factor XIII deficiency in Iran: a comprehensive review of the literatureAkbar Dorgalaleh, Majid Naderi, Maryam Sadat Hosseini, et al.
Pageof 6

Showing results (21-30 of 58) with videos related to

Sort By:
Pageof 6
Turkish Journal of Medical Sciences|August 12, 2016
Childhood acute lymphoblastic leukemia: refusal and abandonmentof treatment in the southeast of IranMajid Naderi, Samira Esmaeili Reykande, Shadi Tabibian, et al.
Hematology (Amsterdam, Netherlands)|December 30, 2014
Association between expression of MMP-2 and MMP-9 genes and pathogenesis of intracranial hemorrhage in severe coagulation factor XIII deficiencyMajid Naderi, Mohammad Reza Younesi, Akbar Dorgalaleh, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 19, 2016
Spectrum of factor X gene mutations in Iranian patients with congenital factor X deficiencyAkbar Dorgalaleh, Farhad Zaker, Shadi Tabibian, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|March 25, 2021
Congenital Combined Bleeding Disorders, a Comprehensive Study of a Large Number of Iranian PatientsSeyed Esmaeil Ahmadi, Mohammad Jazebi, Gholamreza Bahoush, et al.
Laboratory Medicine|August 14, 2016
Comparison of 2 Methods of Clot Solubility Testing in Detection of Factor XIII DeficiencyAkbar Dorgalaleh, Shadi Tabibian, Vahideh Assadollahi, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 3, 2016
Disseminated intravascular coagulation with positive D-dimer: a controversial clinical feature in severe congenital factor XIII deficiency in southeast IranMajid Naderi, Shadi Tabibian, Marzia Menegatti, et al.
International Journal of Hematology|September 19, 2014
Clinical manifestations and management of life-threatening bleeding in the largest group of patients with severe factor XIII deficiencyMajid Naderi, Akbar Dorgalaleh, Shaban Alizadeh, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|July 12, 2025
Identification of novel RASGRP2 mutations in patients with platelet dysfunctionMohadese Heydarali Broojerdi, Shadi Tabibian, Rima Manafi Shabestari, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|April 13, 2024
Molecular and clinical profile of rare bleeding disorders: A single-center retrospective studyArash Ahmadfard Moghadam, Amir Reza Manafzadeh, Mohammad Reza Nikoonia, et al.
Seminars in Thrombosis and Hemostasis|January 24, 2015
Factor XIII deficiency in Iran: a comprehensive review of the literatureAkbar Dorgalaleh, Majid Naderi, Maryam Sadat Hosseini, et al.
Pageof 6