Factor XII deficiency (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Factor XII deficiency" in English language version.

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6nih.gov

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4doi.org

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2web.archive.org

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2semanticscholar.org

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1vcu.edu

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1rarediseases.org

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1schattauer.de

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doi.org

Pauer HU, Burfeind P, Köstering H, Emons G, Hinney B (2003). "Factor XII deficiency is strongly associated with primary recurrent abortions". Fertility and Sterility. 80 (3): 590–594. doi:10.1016/S0015-0282(03)00788-X. PMID 12969703.
Zeerleder S, Schloesser M, Redondo M, Wuillemin WA, Engel W, Furlan M, Laemmle B (1999). "Reevaluation of the Incidence of Thromboembolic Complications in Congenital Factor XII Deficiency A Study on 73 Subjects from 14 Swiss Families". Thrombosis and Haemostasis. 82 (4): 1240–1246. doi:10.1055/s-0037-1614368. PMID 10544906. S2CID 37296883. Archived from the original on February 21, 2017. Retrieved February 20, 2017.
Halbmayer WM, Haushofer A, Schoen R, Mannhalter C, Strohmer E, Baumgarten K, Fischer M (1994). "The prevalence of moderate and severe FXII (Hageman factor) deficiency among the normal population: evaluation of the incidence of FXII deficiency among 300 healthy blood donors". Thromb Haemost. 71 (1): 68–72. doi:10.1055/s-0038-1642386. PMID 8165648. S2CID 39576004.
Cichon S, Martin L, Hennies HC, Müller F, Van Driessche K, Karpushova A, Stevens W, Colombo R, Renné T, Drouet C, Bork K, Nöthen MM (2006). "Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III". Am J Hum Genet. 79 (6): 1098–1104. doi:10.1086/509899. PMC 1698720. PMID 17186468.

nih.gov

pubmed.ncbi.nlm.nih.gov

Pauer HU, Burfeind P, Köstering H, Emons G, Hinney B (2003). "Factor XII deficiency is strongly associated with primary recurrent abortions". Fertility and Sterility. 80 (3): 590–594. doi:10.1016/S0015-0282(03)00788-X. PMID 12969703.
Zeerleder S, Schloesser M, Redondo M, Wuillemin WA, Engel W, Furlan M, Laemmle B (1999). "Reevaluation of the Incidence of Thromboembolic Complications in Congenital Factor XII Deficiency A Study on 73 Subjects from 14 Swiss Families". Thrombosis and Haemostasis. 82 (4): 1240–1246. doi:10.1055/s-0037-1614368. PMID 10544906. S2CID 37296883. Archived from the original on February 21, 2017. Retrieved February 20, 2017.
Halbmayer WM, Haushofer A, Schoen R, Mannhalter C, Strohmer E, Baumgarten K, Fischer M (1994). "The prevalence of moderate and severe FXII (Hageman factor) deficiency among the normal population: evaluation of the incidence of FXII deficiency among 300 healthy blood donors". Thromb Haemost. 71 (1): 68–72. doi:10.1055/s-0038-1642386. PMID 8165648. S2CID 39576004.
Cichon S, Martin L, Hennies HC, Müller F, Van Driessche K, Karpushova A, Stevens W, Colombo R, Renné T, Drouet C, Bork K, Nöthen MM (2006). "Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III". Am J Hum Genet. 79 (6): 1098–1104. doi:10.1086/509899. PMC 1698720. PMID 17186468.
Ratnoff OD, Margolius A (1955). "Hageman trait: an asymptomatic disorder of blood coagulation". Transactions of the Association of American Physicians. 68: 149–54. PMID 13299324.

ncbi.nlm.nih.gov

Cichon S, Martin L, Hennies HC, Müller F, Van Driessche K, Karpushova A, Stevens W, Colombo R, Renné T, Drouet C, Bork K, Nöthen MM (2006). "Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III". Am J Hum Genet. 79 (6): 1098–1104. doi:10.1086/509899. PMC 1698720. PMID 17186468.

rarediseases.org

"Factor XII Deficiency". National Organization for Rare Disorders(NORD). Retrieved February 20, 2017.

schattauer.de

th.schattauer.de

Zeerleder S, Schloesser M, Redondo M, Wuillemin WA, Engel W, Furlan M, Laemmle B (1999). "Reevaluation of the Incidence of Thromboembolic Complications in Congenital Factor XII Deficiency A Study on 73 Subjects from 14 Swiss Families". Thrombosis and Haemostasis. 82 (4): 1240–1246. doi:10.1055/s-0037-1614368. PMID 10544906. S2CID 37296883. Archived from the original on February 21, 2017. Retrieved February 20, 2017.

semanticscholar.org

api.semanticscholar.org

Zeerleder S, Schloesser M, Redondo M, Wuillemin WA, Engel W, Furlan M, Laemmle B (1999). "Reevaluation of the Incidence of Thromboembolic Complications in Congenital Factor XII Deficiency A Study on 73 Subjects from 14 Swiss Families". Thrombosis and Haemostasis. 82 (4): 1240–1246. doi:10.1055/s-0037-1614368. PMID 10544906. S2CID 37296883. Archived from the original on February 21, 2017. Retrieved February 20, 2017.
Halbmayer WM, Haushofer A, Schoen R, Mannhalter C, Strohmer E, Baumgarten K, Fischer M (1994). "The prevalence of moderate and severe FXII (Hageman factor) deficiency among the normal population: evaluation of the incidence of FXII deficiency among 300 healthy blood donors". Thromb Haemost. 71 (1): 68–72. doi:10.1055/s-0038-1642386. PMID 8165648. S2CID 39576004.

vcu.edu

pathology.vcu.edu

Riley RS (April 2005). "Factor XII Deficiency" (PDF). Pathology, Virginia Commonwealth University. Archived from the original (PDF) on February 21, 2017. Retrieved February 20, 2017.

web.archive.org

Riley RS (April 2005). "Factor XII Deficiency" (PDF). Pathology, Virginia Commonwealth University. Archived from the original (PDF) on February 21, 2017. Retrieved February 20, 2017.
Zeerleder S, Schloesser M, Redondo M, Wuillemin WA, Engel W, Furlan M, Laemmle B (1999). "Reevaluation of the Incidence of Thromboembolic Complications in Congenital Factor XII Deficiency A Study on 73 Subjects from 14 Swiss Families". Thrombosis and Haemostasis. 82 (4): 1240–1246. doi:10.1055/s-0037-1614368. PMID 10544906. S2CID 37296883. Archived from the original on February 21, 2017. Retrieved February 20, 2017.