Works matching DE "BLOOD coagulation factor XIII"
Results: 462
Simulating fibrin clotting time.
- Published in:
- Medical & Biological Engineering & Computing, 2006, v. 44, n. 1/2, p. 79, doi. 10.1007/s11517-005-0007-z
- By:
- Publication type:
- Article
Induction of hemodialysis therapy in a case with factor XIII deficiency.
- Published in:
- 2011
- By:
- Publication type:
- Letter
A case of atypical hemolytic uremic syndrome due to anti-factor H antibody in a patient presenting with a factor XII deficiency identified two novel mutations.
- Published in:
- Clinical & Experimental Nephrology, 2011, v. 15, n. 2, p. 269, doi. 10.1007/s10157-010-0375-z
- By:
- Publication type:
- Article
A cross-sectional study to find association of VDR gene polymorphism with non-syndromic congenital ichthyosis and with vitamin D deficiency.
- Published in:
- Archives of Dermatological Research, 2023, v. 315, n. 3, p. 551, doi. 10.1007/s00403-022-02399-z
- By:
- Publication type:
- Article
Cancer, platelet distribution width, and total protein levels as predictors of rebleeding in upper gastrointestinal bleeding.
- Published in:
- PeerJ, 2022, p. 1, doi. 10.7717/peerj.14061
- By:
- Publication type:
- Article
Exploration of the residues modulating the catalytic features of human carbonic anhydrase XIII by a site-specific mutagenesis approach.
- Published in:
- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1506, doi. 10.1080/14756366.2019.1653290
- By:
- Publication type:
- Article
Factor XIII deficiency and head trauma: management and therapy.
- Published in:
- 2015
- By:
- Publication type:
- Letter
Factor XIIIa-positive dermal dendritic cells in keloids and hypertrophic and mature scars.
- Published in:
- Pathology International, 2007, v. 57, n. 6, p. 337, doi. 10.1111/j.1440-1827.2007.02105.x
- By:
- Publication type:
- Article
DETERMINATION OF CYTOKINE STATUS INDICATORS AND ANGIOGENESIS FACTORS IN PATIENTS WITH EXTERNAL GENITAL ENDOMETRIOSIS AND VITAMIN D DEFICIENCY.
- Published in:
- Periódico Tchê Química, 2020, v. 17, n. 34, p. 251, doi. 10.52571/ptq.v17.n34.2020.268_p34_pgs_251_259.pdf
- By:
- Publication type:
- Article
A Comprehensive Update on Late-Onset Pompe Disease.
- Published in:
- Biomolecules (2218-273X), 2023, v. 13, n. 9, p. 1279, doi. 10.3390/biom13091279
- By:
- Publication type:
- Article
The Structure of Blood Coagulation Factor XIII Is Adapted to Oxidation.
- Published in:
- Biomolecules (2218-273X), 2020, v. 10, n. 6, p. 914, doi. 10.3390/biom10060914
- By:
- Publication type:
- Article
EPIDERMAL PROTEASE.
- Published in:
- British Journal of Dermatology, 1955, v. 67, n. 5, p. 201
- Publication type:
- Article
Collagen remodelling and plasma ascorbic acid levels in patients suspected of inherited bleeding disorders harbouring germline variants in collagen‐related genes.
- Published in:
- Haemophilia, 2021, v. 27, n. 1, p. e69, doi. 10.1111/hae.14195
- By:
- Publication type:
- Article
A neonate bearing a novel genetic variant within the factor XIII active site presenting with severe umbilical haemorrhage.
- Published in:
- Haemophilia, 2020, v. 26, n. 6, p. e324, doi. 10.1111/hae.14074
- By:
- Publication type:
- Article
Benefits of thromboelastometry for monitoring replacement therapy in patients with severe inherited factor XIII deficiency: 3 illustrative cases.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. e336, doi. 10.1111/hae.13823
- By:
- Publication type:
- Article
Tailored prophylaxis with rFXIII (NovoThirteen<sup>®</sup>) in a young girl with severe FXIII deficiency and previous cephalohaematoma.
- Published in:
- Haemophilia, 2019, v. 25, n. 3, p. e206, doi. 10.1111/hae.13723
- By:
- Publication type:
- Article
Prophylactic treatment of bleeding episodes in children <12 years with moderate to severe hereditary factor X deficiency (FXD): Efficacy and safety of a high‐purity plasma‐derived factor X (pdFX) concentrate.
- Published in:
- Haemophilia, 2018, v. 24, n. 6, p. 941, doi. 10.1111/hae.13500
- By:
- Publication type:
- Article
Challenges in diagnosis and management of acquired factor XIII (FXIII) inhibitors.
- Published in:
- Haemophilia, 2018, v. 24, n. 6, p. e417, doi. 10.1111/hae.13603
- By:
- Publication type:
- Article
Congenital coagulation factor X deficiency: Genetic analysis of five patients and functional characterization of mutant factor X proteins.
- Published in:
- Haemophilia, 2018, v. 24, n. 5, p. 774, doi. 10.1111/hae.13606
- By:
- Publication type:
- Article
Factor XI deficiency is not associated with an increased risk of pneumonia and pneumonia‐related mortality.
- Published in:
- Haemophilia, 2018, v. 24, n. 4, p. 634, doi. 10.1111/hae.13463
- By:
- Publication type:
- Article
Successful treatment of acquired von Willebrand disease with lenalidomide leading to dramatic resolution of intractable gastrointestinal bleeding: A case report.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla study.
- Published in:
- Haemophilia, 2017, v. 23, n. 6, p. e488, doi. 10.1111/hae.13356
- By:
- Publication type:
- Article
The first case report of a patient with acquired factor XIII deficiency in the context of autoimmune encephalitis.
- Published in:
- Haemophilia, 2017, v. 23, n. 5, p. e461, doi. 10.1111/hae.13281
- By:
- Publication type:
- Article
Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII-A<sub>2</sub>.
- Published in:
- Haemophilia, 2017, v. 23, p. e194, doi. 10.1111/hae.13233
- By:
- Publication type:
- Article
Low bleeding rates with increase or maintenance of physical activity in patients treated with recombinant factor VIII Fc fusion protein ( rFVIIIFc) in the A-LONG and Kids A- LONG Studies.
- Published in:
- Haemophilia, 2017, v. 23, n. 1, p. e39, doi. 10.1111/hae.13125
- By:
- Publication type:
- Article
Rare coagulation disorders: fibrinogen, factor VII and factor XIII.
- Published in:
- Haemophilia, 2016, v. 22, p. 61, doi. 10.1111/hae.12965
- By:
- Publication type:
- Article
Spontaneous splenic rupture accompanied by hepatic arterial dissection in a patient with autoimmune haemorrhaphilia due to anti-factor XIII antibodies.
- Published in:
- Haemophilia, 2016, v. 22, n. 4, p. e314, doi. 10.1111/hae.12940
- By:
- Publication type:
- Article
In vitro comparison of the effect of two factor XI (FXI) concentrates on thrombin generation in major FXI deficiency.
- Published in:
- Haemophilia, 2016, v. 22, n. 3, p. 403, doi. 10.1111/hae.12846
- By:
- Publication type:
- Article
Alloantibody developed in a factor XIII A subunit deficient patient during substitution therapy; characterization of the antibody.
- Published in:
- Haemophilia, 2016, v. 22, n. 2, p. 268, doi. 10.1111/hae.12786
- By:
- Publication type:
- Article
Combined high molecular weight Kininogen and factor XI deficiency.
- Published in:
- Haemophilia, 2016, v. 22, n. 1, p. e60, doi. 10.1111/hae.12835
- By:
- Publication type:
- Article
Clinical features of 32 new Japanese cases with autoimmune haemorrha-philia.
- Published in:
- Haemophilia, 2015, v. 21, n. 5, p. 653, doi. 10.1111/hae.12677
- By:
- Publication type:
- Article
Congenital combined deficiency of coagulation factors VII and X - different genetic mechanisms.
- Published in:
- Haemophilia, 2015, v. 21, n. 3, p. 386, doi. 10.1111/hae.12604
- By:
- Publication type:
- Article
Uneventful long-term anticoagulation with fluindione in a patient with severe factor XI deficiency.
- Published in:
- Haemophilia, 2015, v. 21, n. 1, p. e72, doi. 10.1111/hae.12502
- By:
- Publication type:
- Article
Pharmacokinetics and safety of plasma-derived factor XIII concentrate (human) in patients with congenital factor XIII deficiency.
- Published in:
- Haemophilia, 2015, v. 21, n. 1, p. 95, doi. 10.1111/hae.12505
- By:
- Publication type:
- Article
Efficacy and safety of prophylactic treatment with plasma-derived factor XIII concentrate (human) in patients with congenital factor XIII deficiency.
- Published in:
- Haemophilia, 2015, v. 21, n. 1, p. 102, doi. 10.1111/hae.12524
- By:
- Publication type:
- Article
The use of recombinant factor XIII in a major bleeding episode of a patient with congenital factor XIII deficiency - the first experience.
- Published in:
- Haemophilia, 2015, v. 21, n. 1, p. e118, doi. 10.1111/hae.12591
- By:
- Publication type:
- Article
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.
- Published in:
- Haemophilia, 2014, v. 20, n. 2, p. 255, doi. 10.1111/hae.12298
- By:
- Publication type:
- Article
Changes in factor XIII level during pregnancy.
- Published in:
- Haemophilia, 2014, v. 20, n. 2, p. e144, doi. 10.1111/hae.12345
- By:
- Publication type:
- Article
Pharmacokinetics of recombinant factor XIII in young children with congenital FXIII deficiency and comparison with older patients.
- Published in:
- Haemophilia, 2014, v. 20, n. 1, p. 99, doi. 10.1111/hae.12224
- By:
- Publication type:
- Article
Polymorphism of thrombin-activatable fibrinolysis inhibitor and risk of intracranial haemorrhage in factor XIII deficiency.
- Published in:
- Haemophilia, 2014, v. 20, n. 1, p. e89, doi. 10.1111/hae.12287
- By:
- Publication type:
- Article
The spectrum of factor XI deficiency in Italy.
- Published in:
- Haemophilia, 2014, v. 20, n. 1, p. 106, doi. 10.1111/hae.12257
- By:
- Publication type:
- Article
Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations.
- Published in:
- Haemophilia, 2014, v. 20, n. 1, p. 114, doi. 10.1111/hae.12267
- By:
- Publication type:
- Article
Acquired factor XIII deficiency: still a clinical challenge in the era of novel therapy.
- Published in:
- Haemophilia, 2014, v. 20, n. 1, p. e104, doi. 10.1111/hae.12314
- By:
- Publication type:
- Article
A child with acquired factor XIII deficiency: case report and literature review.
- Published in:
- Haemophilia, 2013, v. 19, n. 6, p. 814, doi. 10.1111/hae.12145
- By:
- Publication type:
- Article
Congenital factor XIII deficiency in women: a systematic review of literature.
- Published in:
- Haemophilia, 2013, v. 19, n. 6, p. e349, doi. 10.1111/hae.12259
- By:
- Publication type:
- Article
Successful treatment of a lung cancer patient with factor XI deficiency.
- Published in:
- Haemophilia, 2013, v. 19, n. 6, p. e367, doi. 10.1111/hae.12260
- By:
- Publication type:
- Article
Pharmacokinetics and prophylactic use of FEIBA<sup>®</sup> in a child with severe congenital factor X deficiency and recurrent spontaneous intracranial haemorrhage: a case report.
- Published in:
- Haemophilia, 2013, v. 19, n. 6, p. e364, doi. 10.1111/hae.12245
- By:
- Publication type:
- Article
Successful delivery in patients with FXIII deficiency receiving prophylaxis: report of 17 cases in Iran.
- Published in:
- Haemophilia, 2012, v. 18, n. 5, p. 773, doi. 10.1111/j.1365-2516.2012.02785.x
- By:
- Publication type:
- Article
Rare bleeding disorders.
- Published in:
- Haemophilia, 2012, v. 18, p. 148, doi. 10.1111/j.1365-2516.2012.02841.x
- By:
- Publication type:
- Article
A case of acquired FXIII deficiency with severe bleeding symptoms.
- Published in:
- Haemophilia, 2012, v. 18, n. 4, p. 618, doi. 10.1111/j.1365-2516.2012.02763.x
- By:
- Publication type:
- Article