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1974 102
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8,388 results

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Page 1
Coagulation Factor X.
[No authors listed] [No authors listed] 2019 Oct 23. Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006–. 2019 Oct 23. Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006–. PMID: 29999949 Free Books & Documents. Review.
Because it is a large protein molecule with a molecular weight of about 40,000, the amount in milk is likely to be very low and absorption is unlikely because it is probably destroyed in the infant's gastrointestinal tract. Until more data become available, coagulation factor …
Because it is a large protein molecule with a molecular weight of about 40,000, the amount in milk is likely to be very low and absorption i …
Factor X deficiency.
Uprichard J, Perry DJ. Uprichard J, et al. Blood Rev. 2002 Jun;16(2):97-110. doi: 10.1054/blre.2002.0191. Blood Rev. 2002. PMID: 12127953 Review.
The gene for factor X maps to the long arm of chromosome 13, approximately 2.8 kb downstream of the factor VII gene. ...The clinical phenotype is of a variable bleeding tendency. Homozygous factor X deficiency has an incidence of 1:1,000,000 in the gen …
The gene for factor X maps to the long arm of chromosome 13, approximately 2.8 kb downstream of the factor VII gene. ...The cl …
Factor X Friuli Coagulation Disorder: Almost 50 Years Later.
Girolami A, Cosi E, Santarossa C, Ferrari S, Girolami B, Lombardi AM. Girolami A, et al. Clin Appl Thromb Hemost. 2018 Jan;24(1):33-40. doi: 10.1177/1076029616686423. Epub 2016 Dec 29. Clin Appl Thromb Hemost. 2018. PMID: 28030967 Free PMC article. Review.
The story of factor X (FX) Friuli. Factor X Friuli was discovered in 1969 to 1970. ...
The story of factor X (FX) Friuli. Factor X Friuli was discovered in 1969 to 1970. ...
Factor X.
Jackson CM. Jackson CM. Prog Hemost Thromb. 1984;7:55-109. Prog Hemost Thromb. 1984. PMID: 6397768 Review. No abstract available.
Diagnosis, therapeutic advances, and key recommendations for the management of factor X deficiency.
Peyvandi F, Auerswald G, Austin SK, Liesner R, Kavakli K, Álvarez Román MT, Millar CM. Peyvandi F, et al. Blood Rev. 2021 Nov;50:100833. doi: 10.1016/j.blre.2021.100833. Epub 2021 Apr 27. Blood Rev. 2021. PMID: 34024682 Free article. Review.
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. ...Consensus in treatment guidelines is still urgently needed to ensure optimal management of patients with factor X deficiency across the spectrum of disease severi …
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. ...Consensus in treatment guidelines is …
Structure and function of factor X: properties, activation, and activity in prothrombinase. A retrospective in a historical context.
Jackson CM. Jackson CM. J Thromb Thrombolysis. 2021 Aug;52(2):371-378. doi: 10.1007/s11239-021-02421-7. Epub 2021 Mar 16. J Thromb Thrombolysis. 2021. PMID: 33725285 Review.
The evolution of our understanding of the formation of thrombin from the postulated thrombokinase of Morawitz to activated Factor X and prothrombinase occurred during a period of nearly 100 years. ...
The evolution of our understanding of the formation of thrombin from the postulated thrombokinase of Morawitz to activated Factor …
Spectrum of factor X gene mutations in Iranian patients with congenital factor X deficiency.
Dorgalaleh A, Zaker F, Tabibian S, Alizadeh S, Dorgalele S, Hosseini S, Shamsizadeh M. Dorgalaleh A, et al. Blood Coagul Fibrinolysis. 2016 Apr;27(3):324-7. doi: 10.1097/MBC.0000000000000435. Blood Coagul Fibrinolysis. 2016. PMID: 26891460 Review.
Congenital factor X deficiency is one of the most severe forms of rare bleeding disorders transmitted in autosomal recessive manner. ...A wide spectrum of factor X gene mutations was observed in Iranian patients with congenital FXD that revealed divers …
Congenital factor X deficiency is one of the most severe forms of rare bleeding disorders transmitted in autosomal recessive m …
Biochemistry of factor X.
Hertzberg M. Hertzberg M. Blood Rev. 1994 Mar;8(1):56-62. doi: 10.1016/0268-960x(94)90007-8. Blood Rev. 1994. PMID: 8205010 Review.
Factor X circulates as a serine protease which is converted to the active form at the point of convergence of the intrinsic and extrinsic coagulation pathways. ...Studies of recombinant proteins and proteolytic fragments continue to provide significant insight into …
Factor X circulates as a serine protease which is converted to the active form at the point of convergence of the intrinsic an …
Plasma-derived human factor X concentrate for on-demand and perioperative treatment in factor X-deficient patients: pharmacology, pharmacokinetics, efficacy, and safety.
Shapiro A. Shapiro A. Expert Opin Drug Metab Toxicol. 2017 Jan;13(1):97-104. doi: 10.1080/17425255.2016.1237504. Epub 2016 Nov 2. Expert Opin Drug Metab Toxicol. 2017. PMID: 27797267 Review.
Hereditary factor X (FX) deficiency is a rare autosomal recessive bleeding disorder characterized mainly by mild-to-severe bleeding into the mucous membranes, muscles or joints. ...
Hereditary factor X (FX) deficiency is a rare autosomal recessive bleeding disorder characterized mainly by mild-to-severe ble …
8,388 results