Hemophilia
LJ Smith - American Society for Clinical Laboratory Science, 2019 - clsjournal.ascls.org
Hemophilia is a rare, congenital bleeding disease with an X-linked recessive inheritance
pattern. It is characterized by absent, decreased, or dysfunctional coagulation factor VIII …
pattern. It is characterized by absent, decreased, or dysfunctional coagulation factor VIII …
[HTML][HTML] Hemophilia A and B: molecular and clinical similarities and differences
G Castaman, D Matino - Haematologica, 2019 - ncbi.nlm.nih.gov
Hemophilia A and B are rare X-linked bleeding disorders caused by mutations in the genes
encoding coagulation factor VIII (FVIII) and factor IX (FIX). Hemophilia A (HA) is more …
encoding coagulation factor VIII (FVIII) and factor IX (FIX). Hemophilia A (HA) is more …
Haemophilia
E Berntorp, K Fischer, DP Hart, ME Mancuso… - Nature reviews Disease …, 2021 - nature.com
Haemophilia A and B are rare congenital, recessive X-linked disorders caused by lack or
deficiency of clotting factor VIII (FVIII) or IX (FIX), respectively. The severity of the disease …
deficiency of clotting factor VIII (FVIII) or IX (FIX), respectively. The severity of the disease …
[BOOK][B] Clinical aspects of non-severe hemophilia: Focus on bleeding, joint and treatment outcomes
FR Kloosterman - 2023 - dare.uva.nl
Hemophilia A and B are rare inherited bleeding disorders, caused by mutations in the F8 or
F9 gene on the X-chromosome leading to a deficiency of coagulation factor VIII (FVIII) or …
F9 gene on the X-chromosome leading to a deficiency of coagulation factor VIII (FVIII) or …
Haemophilia (Primer)
B Erik, F Kathelijn, DP Hart… - Nature Reviews …, 2021 - search.proquest.com
Haemophilia A and B are rare congenital, recessive X-linked disorders caused by lack or
deficiency of clotting factor VIII (FVIII) or IX (FIX), respectively. The severity of the disease …
deficiency of clotting factor VIII (FVIII) or IX (FIX), respectively. The severity of the disease …
Another victory for patients with hemophilia
C Leissinger - New England Journal of Medicine, 2023 - Mass Medical Soc
Congenital hemophilia A is a rare bleeding disorder caused by a mutation in the gene
encoding factor VIII, resulting in a deficiency of factor VIII activity. Severe hemophilia (factor …
encoding factor VIII, resulting in a deficiency of factor VIII activity. Severe hemophilia (factor …
Hemophilia A and B: diagnosis and management
D Brown - … Hematology: Expert Clinical Review: Questions and …, 2016 - Springer
Hemophilia A and B are X-linked recessive disorders caused by deficiency of coagulation
Factors VIII and IX, respectively. Hemophilia A occurs in 1 of 5032 live male births in the …
Factors VIII and IX, respectively. Hemophilia A occurs in 1 of 5032 live male births in the …
Comprehensive approach to hemophilia
V Gök, E Ünal - Journal of Health Sciences and Medicine, 2022 - dergipark.org.tr
Hemophilia A, B are X-linked recessive bleeding disorder that typically results from a
deficiency of clotting factor VIII (FVIII) and factor IX (FIX). The severity of the disease is …
deficiency of clotting factor VIII (FVIII) and factor IX (FIX). The severity of the disease is …
[CITATION][C] Haemophilia A (Factor VIII deficiency) and Haemophilia B (Factor IX deficiency)
C Ryan, B White