Results 81 to 90 of about 12,566,431 (163)

Genetic variation of rs438601 marker in the Iranian Population: An informative marker for molecular diagnosis of hemophilia B

open access: yesMajallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, 2014
Introduction: Hemophilia B is an X-linked recessive genetic disease caused by mutations in the coagulation Factor IX gene. Mutations in the Factor IX gene result in dysfunction or deficiency of coagulation factor of IX.
P Dorri, A Karimi , S Vallian boroujeni
doaj  

Stable and durable factor IX levels in patients with hemophilia B over 3 years after etranacogene dezaparvovec gene therapy. [PDF]

open access: yesBlood Adv, 2023
von Drygalski A   +13 more
europepmc   +1 more source

The mechanism underlying activation of factor IX by factor XIa.

open access: yesThrombosis Research, 2014
D. Gailani   +6 more
semanticscholar   +1 more source

Post hoc longitudinal assessment of the efficacy and safety of recombinant factor IX Fc fusion protein in hemophilia B. [PDF]

open access: yesBlood Adv, 2023
Shapiro AD   +16 more
europepmc   +1 more source

Characteristics and Treatment Patterns of Patients with Haemophilia B Receiving Recombinant Coagulation Factor IX. [PDF]

open access: yesJ Clin Med
Park YS   +16 more
europepmc   +1 more source

Differences in wild-type- and R338L-tenase complex formation are at the root of R338L-factor IX assay discrepancies. [PDF]

open access: yesBlood Adv, 2023
Foley JH   +12 more
europepmc   +1 more source

Long-term outcomes of prophylaxis with a recombinant factor VIII Fc or recombinant factor IX Fc in patients with hemophilia previously treated on demand. [PDF]

open access: yesRes Pract Thromb Haemost, 2023
Álvarez-Román MT   +7 more
europepmc   +1 more source

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