Works matching DE "DYSFIBRINOGENEMIA"
Results: 30
Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization.
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- Haemophilia, 2017, v. 23, n. 4, p. e340, doi. 10.1111/hae.13268
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- Article
Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family.
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- Haemophilia, 2015, v. 21, n. 6, p. 846, doi. 10.1111/hae.12712
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- Article
Participation and risk-taking behaviour in sports in children with haemophilia.
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- Haemophilia, 2009, v. 15, n. 3, p. 686, doi. 10.1111/j.1365-2516.2009.02006.x
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- Article
Factor XIII deficiency in south-east Iran.
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- 2004
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- Publication type:
- Letter
Hypercoagulability in a Patient with Hypodysfibrinogenemia:Implic ations for Clinical Management.
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- Acta Haematologica, 1999, v. 101, n. 4, p. 209, doi. 10.1159/000040956
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- Article
The dysfibrinogenaemias.
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- British Journal of Haematology, 2001, v. 114, n. 2, p. 249, doi. 10.1046/j.1365-2141.2001.02892.x
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- Article
Electrospray ionization mass spectrometry identification of fibrinogen Banks Peninsula (γ280Tyr→Cys): a new variant with defective polymerization.
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- British Journal of Haematology, 1998, v. 101, n. 1, p. 24, doi. 10.1046/j.1365-2141.1998.00663.x
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- Article
Management of inherited dysfibrinogenemia during pregnancy: a description of four consecutive cases.
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- 2007
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- Publication type:
- Letter
A Chinese family with congenital Dysfibrinogenemia carries a heterozygous missense mutation in FGA: Concerning the genetic abnormality and clinical treatment.
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- Pakistan Journal of Medical Sciences, 2017, v. 33, n. 4, p. 1, doi. 10.12669/pjms.334.12828
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- Article
Ventricular Tachycardia in Acute Fulminant Myocarditis: Medical Management and Follow-up.
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- Pediatric Cardiology, 2008, v. 29, n. 2, p. 416, doi. 10.1007/s00246-007-9044-8
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- Article
Disseminated intravascular coagulation after isolated mild head injury.
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- Acta Neurochirurgica, 2009, v. 151, n. 11, p. 1521, doi. 10.1007/s00701-009-0258-9
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- Article
Can Mutations Identified in Congenital Fibrinogen Disorders Explain the Clinical Manifestations?
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- Journal of Coagulation Disorders, 2010, v. 2, n. 2, p. 1
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- Publication type:
- Article
LABORATORY INVESTIGATION OF THROMBOPHILIA.
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- Journal of Medical Biochemistry, 2014, v. 33, n. 1, p. 28, doi. 10.2478/jomb-2013-0041
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- Article
Dysfibrinogenemia and multiple sclerosis: spuriously associated or causally linked?
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- Hippokratia, 2018, v. 21, n. 1, p. 49
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- Publication type:
- Article
Building an immune-mediated coagulopathy consensus: early recognition and evaluation to enhance post-surgical patient safety.
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- Patient Safety in Surgery, 2009, v. 3, p. 1, doi. 10.1186/1754-9493-3-8
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- Publication type:
- Article
Dysfibrinogenemia during pregnancy treated successfully with fibrinogen.
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- 2003
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- Publication type:
- journal article
A novel fibrinogen variant – Liberec: dysfibrinogenaemia associated with γ Tyr262Cys substitution.
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- European Journal of Haematology, 2008, v. 81, n. 2, p. 123, doi. 10.1111/j.1600-0609.2008.01094.x
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- Publication type:
- Article
Disfibrinojenemi ve Homosisteinemili Genç Bir Olguda Nonarteritik Anterior İskemik Optik Nöropati.
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- Retina-Vitreus/Journal of Retina-Vitreous, 2012, v. 20, n. 4, p. 311
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- Article
Use of Chromogenic Assay of Factor X to Accept or Reject INR Results in Warfarin Treated Patients.
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- 2009
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- Case Study
Sneddon Syndrome revealing dysfibrinogenemia.
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- International Journal of Dermatology, 2003, v. 42, n. 7, p. 561, doi. 10.1046/j.1365-4362.2003.01723_1.x
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- Article
Genetic Thrombophilias and Pregnancy Loss.
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- 2006
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- Publication type:
- Editorial
Thromboelastography predicts risks of obstetric complication occurrence in (hypo)dysfibrinogenemia patients under non-pregnant state.
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- Clinical & Experimental Pharmacology & Physiology, 2016, v. 43, n. 2, p. 149, doi. 10.1111/1440-1681.12509
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- Publication type:
- Article
Structural Changes in the Fibrin Network of a Pretoria Family with Dysfibrinogenemia: A Scanning Electron Microscopical Study.
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- Ultrastructural Pathology, 2006, v. 30, n. 3, p. 167, doi. 10.1080/01913120600689772
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- Publication type:
- Article
Presence of Idiopathic Thrombocytopenic Purpura and Autoimmune Hemolytic Anemia in the Patients with Common Variable Immunodeficiency.
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- Iranian Journal of Allergy, Asthma & Immunology, 2008, v. 7, n. 3, p. 169
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- Publication type:
- Article
Hypodysfibrinogenemia with a Heterozygous Mutation of γCys326Ser by the Novel Transversion of TGT to TCT in a Patient with Pulmonary Thromboembolism and Right Ventricular Thrombus.
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- 2017
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- Publication type:
- Case Study
Erythrocyte hyperaggregation and thrombogenic dysfibrinogenemia.
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- Clinical Hemorheology & Microcirculation, 1998, v. 18, n. 4, p. 235
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- Publication type:
- Article
Syndromes of Thrombosis and Hypercoagulability: Congenital and Acquired Thrombophilias.
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- Clinical & Applied Thrombosis/Hemostasis, 1998, v. 4, n. 1, p. 25, doi. 10.1177/107602969800400106
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- Publication type:
- Article
Liver Cirrhosis Manifested by Dysfibrinogenemia.
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- Clinical & Applied Thrombosis/Hemostasis, 1997, v. 3, n. 2, p. 102, doi. 10.1177/107602969700300206
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- Article
Familial Thrombophilia: A Review Analysis.
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- Clinical & Applied Thrombosis/Hemostasis, 1996, v. 2, n. 4, p. 227, doi. 10.1177/107602969600200402
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- Article
Diagnosis and Prognosis.
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- Current Medical Literature: Pulmonary Hypertension, 2010, v. 1, n. 2, p. 52
- Publication type:
- Article