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Quoted phrase not found in phrase index: "Factor VIII and Factor IX, combined deficiency of"
Page 1
Inherited bleeding disorders.
Blanchette VS, Sparling C, Turner C. Blanchette VS, et al. Baillieres Clin Haematol. 1991 Apr;4(2):291-332. doi: 10.1016/s0950-3536(05)80162-3. Baillieres Clin Haematol. 1991. PMID: 1912663 Review.
In clinical practice it is useful to distinguish disorders that cause significant clinical bleeding from those that cause few or no symptoms. Examples of the former include severe deficiencies of factors VIII and IX, and the homozygous forms of factor …
In clinical practice it is useful to distinguish disorders that cause significant clinical bleeding from those that cause few or no symptoms …
Treatment of inherited platelet disorders.
Seligsohn U. Seligsohn U. Haemophilia. 2012 Jul;18 Suppl 4:161-5. doi: 10.1111/j.1365-2516.2012.02842.x. Haemophilia. 2012. PMID: 22726101 Review.
(iv) Desmopressin that increases plasma levels of von Willebrand factor and factor VIII giving rise to increased platelet adhesiveness and aggregation associated with shortened bleeding time. (v) Recombinant factor VIIa (rFVIIa). GT patients have been …
(iv) Desmopressin that increases plasma levels of von Willebrand factor and factor VIII giving rise to increased platel …
A Review of Factor VIII and Factor IX Assay Methods for Monitoring Extended Half-Life Products in Hemophilia A and B.
Abraham S, Duncan EM. Abraham S, et al. Methods Mol Biol. 2023;2663:569-588. doi: 10.1007/978-1-0716-3175-1_37. Methods Mol Biol. 2023. PMID: 37204737 Review.
Clinical trials have used a variety of coagulation factor assay methods to assess treatment with recombinant Factor VIII (rFVIII) and recombinant Factor IX (rFIX) extended half-life (EHL) products. However, diagnostic laboratories may use differ …
Clinical trials have used a variety of coagulation factor assay methods to assess treatment with recombinant Factor VIII …
Hemophilic joint disease - current perspective and potential future strategies.
Acharya SS. Acharya SS. Transfus Apher Sci. 2008 Feb;38(1):49-55. doi: 10.1016/j.transci.2007.12.006. Epub 2008 Mar 4. Transfus Apher Sci. 2008. PMID: 18304874 Review.
Recurrent hemarthroses can lead to hemophilic joint disease (HJD), which is one of the most disabling complications of these X-linked recessive disorders characterized by a deficiency of clotting factors VIII/IX. The pathogenesis of HJD is not well understood …
Recurrent hemarthroses can lead to hemophilic joint disease (HJD), which is one of the most disabling complications of these X-linked recess …
Hemophilia A and factor V deficiency in a girl with Turner syndrome: a case report.
Al Khudari R, Batesh D, Habash R, Hamdn O. Al Khudari R, et al. J Med Case Rep. 2023 Nov 18;17(1):480. doi: 10.1186/s13256-023-04215-2. J Med Case Rep. 2023. PMID: 37978530 Free PMC article.
The lab tests showed: prolonged activated partial thromboplastin time and prothrombin time with deficiency of factor V (1%) and factor VIII (1%). We diagnosed hemophilia A with factor V deficiency. ...CONCLUSIONS: In females affected with …
The lab tests showed: prolonged activated partial thromboplastin time and prothrombin time with deficiency of factor V (1%) an …
"Familial Multiple Coagulation Factor Deficiencies of FXI and FXII in an Asymptomatic Saudi Woman".
Al-Ansari RY, Alruwaili AF, Alqahtani KM, Al-Harbi AF, Woodman A. Al-Ansari RY, et al. J Investig Med High Impact Case Rep. 2023 Jan-Dec;11:23247096231199413. doi: 10.1177/23247096231199413. J Investig Med High Impact Case Rep. 2023. PMID: 37705386 Free PMC article.
Factor XI deficiency (FXI) is the third most common coagulation factor deficiency after hemophilia A and B, ie, in the hierarchy after factors VIII and IX, taking into account von Willebrand's factor deficiency, as bleeding …
Factor XI deficiency (FXI) is the third most common coagulation factor deficiency after hemophilia A and B, ie, …
Carrier and prenatal diagnostic strategy and newly identified mutations in Hungarian haemophilia A and B families.
Bors A, Andrikovics H, Illés Z, Jáger R, Kardos M, Marosi A, Nemes L, Tordai A. Bors A, et al. Blood Coagul Fibrinolysis. 2015 Mar;26(2):161-6. doi: 10.1097/MBC.0000000000000212. Blood Coagul Fibrinolysis. 2015. PMID: 25255241
Deficiencies of blood coagulation factors VIII and IX (haemophilia A and haemophilia B) represent the most common inherited bleeding disorders with a wide range of causative mutations. Carrier and prenatal diagnostics are preferably performed by direct mutati …
Deficiencies of blood coagulation factors VIII and IX (haemophilia A and haemophilia B) represent the most common inher …
Combined coagulation factor VIII and factor IX deficiency (CDF8F9) in a patient from Lithuania.
Ivaškevičius V, Pezeshkpoor B, Biswas A, Goldmann G, Horneff S, Gimbutyte M, Malciute L, Jurgutis R, Oldenburg J. Ivaškevičius V, et al. Hamostaseologie. 2016 Nov 8;36(Suppl. 2):S29-S33. Hamostaseologie. 2016. PMID: 27824213
Haemophilia A (FVIII deficiency) and haemophilia B (FIX deficiency) are X-linked inherited bleeding disorders. It is a very rare event to identify both haemophilias in the same patient. So far, only two families with such combination are reported in the liter …
Haemophilia A (FVIII deficiency) and haemophilia B (FIX deficiency) are X-linked inherited bleeding disorders. It is a very ra …
Autosomal recessive inherited bleeding disorders in Pakistan: a cross-sectional study from selected regions.
Naz A, Jamal MY, Amanat S, Din Ujjan I, Najmuddin A, Patel H, Raziq F, Ahmed N, Imran A, Shamsi TS. Naz A, et al. Orphanet J Rare Dis. 2017 Apr 7;12(1):66. doi: 10.1186/s13023-017-0620-6. Orphanet J Rare Dis. 2017. PMID: 28388959 Free PMC article.
Out of 211 patients with ARBD; 95 (33.8%) had vWD type 3. Fibrinogen deficiency was found in 34 patients (12%), GT in 27 (9.6%), factor XIII deficiency in 13 (4.6%), factor VII deficiency in 12 (4.3%), factor V deficiency in 9 (3.2 …
Out of 211 patients with ARBD; 95 (33.8%) had vWD type 3. Fibrinogen deficiency was found in 34 patients (12%), GT in 27 (9.6%), f …
Orthopedic management of hemophilia.
Heyworth BE, Su EP, Figgie MP, Acharya SS, Sculco TP. Heyworth BE, et al. Am J Orthop (Belle Mead NJ). 2005 Oct;34(10):479-86. Am J Orthop (Belle Mead NJ). 2005. PMID: 16304795 Review.
Hemophilia is an X-linked inherited bleeding disorder characterized by a deficiency of clotting factor VIII or IX in the intrinsic pathway of the coagulation cascade. This disease can have a profound, debilitating effect on the musculoskeletal system t …
Hemophilia is an X-linked inherited bleeding disorder characterized by a deficiency of clotting factor VIII or IX …
26 results