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Factor XIII deficiency diagnosis: Challenges and tools.
- Published in:
- International Journal of Laboratory Hematology, 2018, v. 40, n. 1, p. 3, doi. 10.1111/ijlh.12756
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- Publication type:
- Article
Potential misdiagnosis of dysfibrinogenaemia: Data from multicentre studies amongst UK NEQAS and PRO-RBDD project laboratories.
- Published in:
- International Journal of Laboratory Hematology, 2017, v. 39, n. 6, p. 653, doi. 10.1111/ijlh.12721
- By:
- Publication type:
- Article
Detection of Factor XIII deficiency: data from multicentre exercises amongst UK NEQAS and PRO- RBDD project laboratories.
- Published in:
- International Journal of Laboratory Hematology, 2017, v. 39, n. 4, p. 350, doi. 10.1111/ijlh.12633
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- Publication type:
- Article
The effect of prion reduction in solvent/detergent-treated plasma on haemostatic variables.
- Published in:
- Vox Sanguinis, 2010, v. 99, n. 3, p. 232, doi. 10.1111/j.1423-0410.2010.01346.x
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- Publication type:
- Article
Reduced circulating FABP2 in patients with moderate to severe COVID-19 may indicate enterocyte functional change rather than cell death.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-23282-x
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- Publication type:
- Article
Genome-wide association studies in myocardial infarction and coronary artery disease.
- Published in:
- 2010
- By:
- Publication type:
- Journal Article
Predikce vzniku inhibitoru faktoru VIII v kohortě SIPPET pomocí analýzy mutací a měření antigenu faktoru VIII.
- Published in:
- Transfusiology & Haematology Today / Transfuze a Hematologie Dnes, 2018, v. 24, n. 2, p. 103
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- Publication type:
- Article
Lombardy diagnostic and therapeutic network of thrombotic microangiopathy.
- Published in:
- 2022
- By:
- Publication type:
- journal article
European principles of inhibitor management in patients with haemophilia: implications of new treatment options.
- Published in:
- 2020
- By:
- Publication type:
- Letter
Evolution of Haemophilia Care in Europe: 10 years of the principles of care.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India.
- Published in:
- Haemophilia, 2007, v. 13, n. 4, p. 413, doi. 10.1111/j.1365-2516.2007.01477.x
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- Publication type:
- Article
Genetic diagnosis of haemophilia and other inherited bleeding disorders.
- Published in:
- Haemophilia, 2006, v. 12, p. 82, doi. 10.1111/j.1365-2516.2006.01263.x
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- Publication type:
- Article
Rare bleeding disorders.
- Published in:
- Haemophilia, 2006, v. 12, p. 137, doi. 10.1111/j.1365-2516.2006.01271.x
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- Publication type:
- Article
Comparison of attitudes towards prenatal diagnosis and termination of pregnancy for haemophilia in Iran and Italy.
- Published in:
- Haemophilia, 2004, v. 10, n. 4, p. 367, doi. 10.1111/j.1365-2516.2004.00927.x
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- Publication type:
- Article
Rare coagulation deficiencies.
- Published in:
- Haemophilia, 2002, v. 8, n. 3, p. 308, doi. 10.1046/j.1365-2516.2002.00633.x
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- Publication type:
- Article
Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency.
- Published in:
- Haemophilia, 1997, v. 3, n. 4, p. 242, doi. 10.1046/j.1365-2516.1997.00137.x
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- Publication type:
- Article
Presentation and pattern of symptoms in 382 patients with Glanzmann thrombasthenia in Iran.
- Published in:
- American Journal of Hematology, 2004, v. 77, n. 2, p. 198, doi. 10.1002/ajh.20159
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- Publication type:
- Article
Variants of OCTN1–2 cation transporter genes are associated with both Crohn's disease and ulcerative colitis.
- Published in:
- Alimentary Pharmacology & Therapeutics, 2006, v. 23, n. 4, p. 497, doi. 10.1111/j.1365-2036.2006.02780.x
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- Publication type:
- Article
Prospective study on the behaviour of the metalloprotease ADAMTS13 and of von Willebrand factor after bone marrow transplantation.
- Published in:
- British Journal of Haematology, 2006, v. 134, n. 2, p. 187, doi. 10.1111/j.1365-2141.2006.06126.x
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- Publication type:
- Article
Clinical manifestations and complications of childbirth and replacement therapy in 385 Iranian patients with type 3 von Willebrand disease.
- Published in:
- British Journal of Haematology, 2000, v. 111, n. 4, p. 1236, doi. 10.1046/j.1365-2141.2000.02507.x
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- Publication type:
- Article
Role of the 2 adenine (g.11293_11294insAA) insertion polymorphism in the 3′ untranslated region of the factor VII (FVII) gene: molecular characterization of a patient with severe FVII deficiency.
- Published in:
- Human Mutation, 2005, v. 26, n. 5, p. 455, doi. 10.1002/humu.20241
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- Publication type:
- Article
Choices of factor VIII products in previously untreated patients with haemophilia A: A global survey.
- Published in:
- Haemophilia, 2018, v. 24, n. 4, p. e266, doi. 10.1111/hae.13535
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- Publication type:
- Article
Differential diagnosis between type 2A and 2B von Willebrand disease in a child with a previously undescribed de novo mutation.
- Published in:
- Haemophilia, 2018, v. 24, n. 4, p. e263, doi. 10.1111/hae.13532
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- Publication type:
- Article
“In vitro” correction of the severe factor V deficiency‐related coagulopathy by a novel plasma‐derived factor V concentrate.
- Published in:
- Haemophilia, 2018, v. 24, n. 4, p. 648, doi. 10.1111/hae.13465
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- Publication type:
- Article
First‐year results of an expanded humanitarian aid programme for haemophilia in resource‐constrained countries.
- Published in:
- Haemophilia, 2018, v. 24, n. 2, p. 229, doi. 10.1111/hae.13409
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- Publication type:
- Article
Molecular investigation of 41 patients affected by coagulation factor XI deficiency.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
A comparative evaluation of a new fully automated assay for von Willebrand factor collagen binding activity to an established method.
- Published in:
- Haemophilia, 2018, v. 24, n. 1, p. 156, doi. 10.1111/hae.13371
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- Publication type:
- Article
Acquired Von Willebrand syndrome and response to desmopressin.
- Published in:
- Haemophilia, 2018, v. 24, n. 1, p. e25, doi. 10.1111/hae.13382
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- Publication type:
- Article
Ageing successfully with haemophilia: A multidisciplinary programme.
- Published in:
- Haemophilia, 2018, v. 24, n. 1, p. 57, doi. 10.1111/hae.13308
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- Publication type:
- Article
Polypharmacy in older adults with severe haemophilia.
- Published in:
- Haemophilia, 2018, v. 24, n. 1, p. e1, doi. 10.1111/hae.13262
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- Publication type:
- Article
Involvement of the IgE-basophil system and mild complement activation in haemophilia B with anti-factor IX neutralizing antibodies and anaphylaxis.
- Published in:
- Haemophilia, 2017, v. 23, n. 4, p. e348, doi. 10.1111/hae.13282
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- Publication type:
- Article
Kreuth IV: European consensus proposals for treatment of haemophilia with coagulation factor concentrates.
- Published in:
- Haemophilia, 2017, v. 23, p. 370, doi. 10.1111/hae.13211
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- Publication type:
- Article
SIPPET: methodology, analysis and generalizability.
- Published in:
- Haemophilia, 2017, v. 23, p. 353, doi. 10.1111/hae.13203
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- Publication type:
- Article
Reply to the letter by Iorio.
- Published in:
- Haemophilia, 2017, v. 23, p. e248, doi. 10.1111/hae.13248
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- Publication type:
- Article
Molecular diagnosis of von Willebrand disease.
- Published in:
- Haemophilia, 2017, v. 23, n. 2, p. 188, doi. 10.1111/hae.13175
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- Publication type:
- Article
Incidence of low-titre factor VIII inhibitors in patients with haemophilia A: meta-analysis of observational studies.
- Published in:
- Haemophilia, 2017, v. 23, n. 2, p. e87, doi. 10.1111/hae.13193
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- Publication type:
- Article
Inhibitor development in haemophilia.
- Published in:
- Haemophilia, 2017, v. 23, p. 3, doi. 10.1111/hae.13145
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- Publication type:
- Article
New Findings on Inhibitor Development: from Registries to Clinical Studies.
- Published in:
- Haemophilia, 2017, v. 23, p. 4, doi. 10.1111/hae.13137
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- Publication type:
- Article
von Willebrand disease type 1 mutation p.Arg1379Cys and the variant p.Ala1377Val synergistically determine a 2M phenotype in four Italian patients.
- Published in:
- Haemophilia, 2016, v. 22, n. 6, p. e502, doi. 10.1111/hae.13084
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- Publication type:
- Article
Genomic approaches to bleeding disorders.
- Published in:
- Haemophilia, 2016, v. 22, p. 42, doi. 10.1111/hae.12998
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- Publication type:
- Article
The thrombin generation assay distinguishes inhibitor from non-inhibitor patients with severe haemophilia A.
- Published in:
- Haemophilia, 2016, v. 22, n. 4, p. e286, doi. 10.1111/hae.12927
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- Publication type:
- Article
Low thrombin generation during major orthopaedic surgery fails to predict the bleeding risk in inhibitor patients treated with bypassing agents.
- Published in:
- Haemophilia, 2016, v. 22, n. 4, p. e292, doi. 10.1111/hae.12939
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- Publication type:
- Article
Baseline factor VIII plasma levels and age at first bleeding in patients with severe forms of von Willebrand disease.
- Published in:
- Haemophilia, 2016, v. 22, n. 4, p. 564, doi. 10.1111/hae.12900
- By:
- Publication type:
- Article
Efficacy, safety and pharmacokinetics of a new high-purity factor X concentrate in subjects with hereditary factor X deficiency.
- Published in:
- Haemophilia, 2016, v. 22, n. 3, p. 419, doi. 10.1111/hae.12893
- By:
- Publication type:
- Article
Long-term prophylaxis in severe factor VII deficiency.
- Published in:
- Haemophilia, 2015, v. 21, n. 6, p. 812, doi. 10.1111/hae.12702
- By:
- Publication type:
- Article
Management of pregnancy in type 2B von Willebrand disease: case report and literature review.
- Published in:
- Haemophilia, 2015, v. 21, n. 1, p. e98, doi. 10.1111/hae.12580
- By:
- Publication type:
- Article
Research in haemophilia B - approaching the request for high evidence levels in a rare disease.
- Published in:
- Haemophilia, 2015, v. 21, n. 1, p. 4, doi. 10.1111/hae.12603
- By:
- Publication type:
- Article
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women.
- Published in:
- Haemophilia, 2014, v. 20, n. 6, p. e377, doi. 10.1111/hae.12514
- By:
- Publication type:
- Article
Management of orthopaedic surgery in rare bleeding disorders.
- Published in:
- Haemophilia, 2014, v. 20, n. 5, p. 693, doi. 10.1111/hae.12387
- By:
- Publication type:
- Article
Does the orphan medicinal product regulation assist or hinder access to innovative haemophilia treatment in Europe?
- Published in:
- 2014
- By:
- Publication type:
- Editorial