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Items: 1 to 20 of 314

1.

Biology of Factor XIII and clinical manifestations of Factor XIII deficiency.

Levy JH, Greenberg C.

Transfusion. 2013 May;53(5):1120-31. doi: 10.1111/j.1537-2995.2012.03865.x. Epub 2012 Aug 28. Review.

PMID:
22928875
2.

Factor XIII deficiency.

Hsieh L, Nugent D.

Haemophilia. 2008 Nov;14(6):1190-200. doi: 10.1111/j.1365-2516.2008.01857.x. Review.

PMID:
19141159
3.

Factor XIII Deficiency.

Karimi M, Bereczky Z, Cohan N, Muszbek L.

Semin Thromb Hemost. 2009 Jun;35(4):426-38. doi: 10.1055/s-0029-1225765. Epub 2009 Jul 13. Review.

PMID:
19598071
4.

Factor XIII: congenital deficiency factor XIII, acquired deficiency, factor XIII A-subunit, and factor XIII B-subunit.

Tahlan A, Ahluwalia J.

Arch Pathol Lab Med. 2014 Feb;138(2):278-81. doi: 10.5858/arpa.2012-0639-RS. Review.

PMID:
24476525
5.

Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired forms.

Biswas A, Ivaskevicius V, Thomas A, Oldenburg J.

Hamostaseologie. 2014;34(2):160-6. doi: 10.5482/HAMO-13-08-0046. Epub 2014 Feb 7. Review.

PMID:
24503678
6.

Congenital factor XIII deficiency in Switzerland: from the worldwide first case in 1960 to its molecular characterisation in 2005.

Schroeder V, Durrer D, Meili E, Schubiger G, Kohler HP.

Swiss Med Wkly. 2007 May 19;137(19-20):272-8. Review.

PMID:
17594539
7.

Factor XIII deficiency: an update.

Schroeder V, Kohler HP.

Semin Thromb Hemost. 2013 Sep;39(6):632-41. doi: 10.1055/s-0033-1353392. Epub 2013 Aug 8. Review.

PMID:
23929307
8.

Severe congenital factor XIII deficiency caused by novel W187X and G273V mutations in the F13A gene; diagnosis and classification according to the ISTH/SSC guidelines.

Souri M, Biswas A, Misawa M, Omura H, Ichinose A.

Haemophilia. 2014 Mar;20(2):255-62. doi: 10.1111/hae.12298. Epub 2013 Nov 29.

PMID:
24286209
9.

Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations.

Katona É, Muszbek L, Devreese K, Kovács KB, Bereczky Z, Jonkers M, Shemirani AH, Mondelaers V, Ermens AA.

Haemophilia. 2014 Jan;20(1):114-20. doi: 10.1111/hae.12267. Epub 2013 Oct 1.

PMID:
24118344
10.

Congenital blood coagulation factor XIII deficiency and perinatal management.

Ichinose A, Asahina T, Kobayashi T.

Curr Drug Targets. 2005 Aug;6(5):541-9. Review.

PMID:
16026274
11.

[Factor XIII in man: a review].

Dufner GS, Marbet GA.

Hamostaseologie. 2002 Feb;22(1):11-9. Review. German.

PMID:
12193980
12.

Acquired plasma factor XIII deficiencies.

Tosetto A, Castaman G, Rodeghiero F.

Haematologica. 1993 Nov-Dec;78(6 Suppl 2):5-10. Review.

PMID:
8039759
13.

Delayed umbilical bleeding--a presenting feature for factor XIII deficiency: clinical features, genetics, and management.

Anwar R, Minford A, Gallivan L, Trinh CH, Markham AF.

Pediatrics. 2002 Feb;109(2):E32.

PMID:
11826242
14.

Molecular modeling predicts structural changes in the A subunit of factor XIII caused by two novel mutations identified in a neonate with severe congenital factor XIII deficiency.

Souri M, Yee VC, Fujii N, Ichinose A.

Thromb Res. 2012 Sep;130(3):506-10. doi: 10.1016/j.thromres.2012.05.003. Epub 2012 May 25.

PMID:
22633530
15.

Molecular mechanism of a mild phenotype in coagulation factor XIII (FXIII) deficiency: a splicing mutation permitting partial correct splicing of FXIII A-subunit mRNA.

Mikkola H, Muszbek L, Laiho E, Syrjälä M, Hämäläinen E, Haramura G, Salmi T, Peltonen L, Palotie A.

Blood. 1997 Feb 15;89(4):1279-87.

16.

Use of Factor XIII (FXIII) concentrate in patients with congenital FXIII deficiency undergoing surgical procedures.

Janbain M, Nugent DJ, Powell JS, St-Louis J, Frame VB, Leissinger CA.

Transfusion. 2015 Jan;55(1):45-50. doi: 10.1111/trf.12784. Epub 2014 Jul 29.

PMID:
25070582
17.

Alloantibodies against the B subunit of plasma factor XIII developed in its congenital deficiency.

Wada H, Souri M, Matsumoto R, Sugihara T, Ichinose A.

Thromb Haemost. 2013 Apr;109(4):661-8. doi: 10.1160/TH12-12-0936. Epub 2013 Feb 14.

PMID:
23407795
18.

Factor XIII: inherited and acquired deficiency.

Board PG, Losowsky MS, Miloszewski KJ.

Blood Rev. 1993 Dec;7(4):229-42. Review.

PMID:
8130686
19.

Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.

Borhany M, Handrkova H, Cairo A, Schroeder V, Fatima N, Naz A, Amanat S, Shamsi T, Peyvandi F, Kohler HP.

Haemophilia. 2014 Jul;20(4):568-74. doi: 10.1111/hae.12340. Epub 2013 Dec 16.

PMID:
24329762
20.

Efficacy and safety of prophylactic treatment with plasma-derived factor XIII concentrate (human) in patients with congenital factor XIII deficiency.

Ashley C, Chang E, Davis J, Mangione A, Frame V, Nugent DJ.

Haemophilia. 2015 Jan;21(1):102-8. doi: 10.1111/hae.12524. Epub 2014 Nov 7.

PMID:
25377187

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