凝血因子 XIII 缺乏症。 - Suppr

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超能文献

Factor XIII deficiency.

作者信息

Anwar R, Miloszewski K J

机构信息

Molecular Medicine Unit, University of Leeds, St. James University, UK.

出版信息

Br J Haematol. 1999 Dec;107(3):468-84. doi: 10.1046/j.1365-2141.1999.01648.x.

DOI:10.1046/j.1365-2141.1999.01648.x

PMID:10583246

Abstract

摘要

相似文献

Factor XIII deficiency.

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引用本文的文献

Clinical Profile of Congenital Factor XIII Deficiency in Children.

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Factor XIII-A: An Indispensable "Factor" in Haemostasis and Wound Healing.

Int J Mol Sci. 2021 Mar 17;22(6):3055. doi: 10.3390/ijms22063055.

Factor XIII and Fibrin Clot Properties in Acute Venous Thromboembolism.

Int J Mol Sci. 2021 Feb 5;22(4):1607. doi: 10.3390/ijms22041607.

Factor XIII-A in Diseases: Role Beyond Blood Coagulation.

Int J Mol Sci. 2021 Feb 1;22(3):1459. doi: 10.3390/ijms22031459.

Dental Management of Factor XIII Deficiency Patients: A Case Series.

Int J Clin Pediatr Dent. 2020 May-Jun;13(3):299-302. doi: 10.5005/jp-journals-10005-1760.

Meta-Analysis of Factor V, Factor VII, Factor XII, and Factor XIII-A Gene Polymorphisms and Ischemic Stroke.

Medicina (Kaunas). 2019 Apr 11;55(4):101. doi: 10.3390/medicina55040101.

Successful treatment of severe gastrointestinal manifestations of Henoch-Schonlein Purpura and factor XIII deficiency using cryoprecipitate transfusion.

Int J Pediatr Adolesc Med. 2015 Jun;2(2):84-88. doi: 10.1016/j.ijpam.2015.06.003. Epub 2015 Jul 26.

Rare congenital bleeding disorders.

Ann Transl Med. 2018 Sep;6(17):331. doi: 10.21037/atm.2018.08.34.

Inhibition of Fibrinolysis by Coagulation Factor XIII.

Biomed Res Int. 2017;2017:1209676. doi: 10.1155/2017/1209676. Epub 2017 Jul 6.

Genomic variants reveal differential evolutionary constraints on human transglutaminases and point towards unrecognized significance of transglutaminase 2.

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相似文献

Factor XIII deficiency.

Br J Haematol. 1999 Dec;107(3):468-84. doi: 10.1046/j.1365-2141.1999.01648.x.

Factor XIII: inherited and acquired deficiency.

Blood Rev. 1993 Dec;7(4):229-42. doi: 10.1016/0268-960x(93)90010-2.

Identification of two novel missense mutations causing severe factor XIII deficiency.

Haemophilia. 2015 May;21(3):e253-e256. doi: 10.1111/hae.12663. Epub 2015 Mar 31.

[Factor XIII deficiency due to lack of both the S and A subunits. (Classification of factor XIII deficiency in 2 groups)].

Ric Clin Lab. 1979;9(2 Suppl):35-49.

Spontaneous splenic rupture in a patient with factor XIII deficiency and a novel mutation.

Pediatr Blood Cancer. 2008 Jan;50(1):113-4. doi: 10.1002/pbc.20786.

Factor XIII deficiency: an update.

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

Factor XIII Deficiency in Western Afghanistan due to a Novel F13A Gene Mutation.

Int J Lab Hematol. 2020 Feb;42(1):e1-e3. doi: 10.1111/ijlh.13050. Epub 2019 May 28.

Factor XIII Deficiency: A Review of Clinical Presentation and Management.

Hematol Oncol Clin North Am. 2021 Dec;35(6):1171-1180. doi: 10.1016/j.hoc.2021.07.009. Epub 2021 Oct 2.

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

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

First trimester prenatal diagnosis of severe FXIII deficiency.

Haemophilia. 2016 Sep;22(5):e443-4. doi: 10.1111/hae.12982. Epub 2016 Jun 24.

引用本文的文献

Clinical Profile of Congenital Factor XIII Deficiency in Children.

Indian J Pediatr. 2024 Mar;91(3):223-228. doi: 10.1007/s12098-023-04681-y. Epub 2023 Jun 14.

Factor XIII-A: An Indispensable "Factor" in Haemostasis and Wound Healing.

Int J Mol Sci. 2021 Mar 17;22(6):3055. doi: 10.3390/ijms22063055.

Factor XIII and Fibrin Clot Properties in Acute Venous Thromboembolism.

Int J Mol Sci. 2021 Feb 5;22(4):1607. doi: 10.3390/ijms22041607.

Factor XIII-A in Diseases: Role Beyond Blood Coagulation.

Int J Mol Sci. 2021 Feb 1;22(3):1459. doi: 10.3390/ijms22031459.

Dental Management of Factor XIII Deficiency Patients: A Case Series.

Int J Clin Pediatr Dent. 2020 May-Jun;13(3):299-302. doi: 10.5005/jp-journals-10005-1760.

Meta-Analysis of Factor V, Factor VII, Factor XII, and Factor XIII-A Gene Polymorphisms and Ischemic Stroke.

Medicina (Kaunas). 2019 Apr 11;55(4):101. doi: 10.3390/medicina55040101.

Successful treatment of severe gastrointestinal manifestations of Henoch-Schonlein Purpura and factor XIII deficiency using cryoprecipitate transfusion.

Int J Pediatr Adolesc Med. 2015 Jun;2(2):84-88. doi: 10.1016/j.ijpam.2015.06.003. Epub 2015 Jul 26.

Rare congenital bleeding disorders.

Ann Transl Med. 2018 Sep;6(17):331. doi: 10.21037/atm.2018.08.34.

Inhibition of Fibrinolysis by Coagulation Factor XIII.

Biomed Res Int. 2017;2017:1209676. doi: 10.1155/2017/1209676. Epub 2017 Jul 6.

Genomic variants reveal differential evolutionary constraints on human transglutaminases and point towards unrecognized significance of transglutaminase 2.

PLoS One. 2017 Mar 1;12(3):e0172189. doi: 10.1371/journal.pone.0172189. eCollection 2017.