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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
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
Choices of factor VIII products in previously untreated patients with haemophilia A: A global survey.
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- Haemophilia, 2018, v. 24, n. 4, p. e266, doi. 10.1111/hae.13535
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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.
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- 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.
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- 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
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- Publication type:
- Letter to the Editor
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
A comparative evaluation of a new fully automated assay for von Willebrand factor collagen binding activity to an established method.
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- Haemophilia, 2018, v. 24, n. 1, p. 156, doi. 10.1111/hae.13371
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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
Ageing successfully with haemophilia: A multidisciplinary programme.
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- Haemophilia, 2018, v. 24, n. 1, p. 57, doi. 10.1111/hae.13308
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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.
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- 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.
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- 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.
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- Haemophilia, 2017, v. 23, n. 2, p. e87, doi. 10.1111/hae.13193
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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
Inhibitor development in haemophilia.
- Published in:
- Haemophilia, 2017, v. 23, p. 3, doi. 10.1111/hae.13145
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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.
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- 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.
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- 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.
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- 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.
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- Haemophilia, 2016, v. 22, n. 4, p. 564, doi. 10.1111/hae.12900
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- 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
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- 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
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- Publication type:
- Article
Management of pregnancy in type 2B von Willebrand disease: case report and literature review.
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- Haemophilia, 2015, v. 21, n. 1, p. e98, doi. 10.1111/hae.12580
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- Publication type:
- Article
Research in haemophilia B - approaching the request for high evidence levels in a rare disease.
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- Haemophilia, 2015, v. 21, n. 1, p. 4, doi. 10.1111/hae.12603
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- Publication type:
- Article
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women.
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- Haemophilia, 2014, v. 20, n. 6, p. e377, doi. 10.1111/hae.12514
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- Publication type:
- Article
Management of orthopaedic surgery in rare bleeding disorders.
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- Haemophilia, 2014, v. 20, n. 5, p. 693, doi. 10.1111/hae.12387
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- Publication type:
- Article
Does the orphan medicinal product regulation assist or hinder access to innovative haemophilia treatment in Europe?
- Published in:
- 2014
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- Publication type:
- Editorial
Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.
- Published in:
- Haemophilia, 2014, v. 20, n. 4, p. 568, doi. 10.1111/hae.12340
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- Publication type:
- Article
Joint WFH-ISTH session: issues in clinical trial design.
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- Haemophilia, 2014, v. 20, p. 137, doi. 10.1111/hae.12415
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- Publication type:
- Article
Rare bleeding disorders - bleeding assessment tools, laboratory aspects and phenotype and therapy of FXI deficiency.
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- Haemophilia, 2014, v. 20, p. 71, doi. 10.1111/hae.12402
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- Publication type:
- Article
Joint WFH- ISTH session: issues in clinical trial design.
- Published in:
- Haemophilia, 2014, v. 20, p. 137, doi. 10.1111/hae.12415
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- Publication type:
- Article
Assaying FVIII activity: one method is not enough, and never was.
- Published in:
- 2014
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- Publication type:
- Editorial
Rare bleeding disorders - bleeding assessment tools, laboratory aspects and phenotype and therapy of FXI deficiency.
- Published in:
- Haemophilia, 2014, v. 20, p. 71, doi. 10.1111/hae.12402
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- 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
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- Publication type:
- Article
Integrated postural analysis in children with haemophilia.
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- Haemophilia, 2014, v. 20, n. 2, p. 263, doi. 10.1111/hae.12369
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- Publication type:
- Article
Orthopaedic surgery in patients with von Willebrand disease.
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- Haemophilia, 2014, v. 20, n. 1, p. 133, doi. 10.1111/hae.12258
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- Publication type:
- Article
A two-centre comparative evaluation of new automated assays for von Willebrand factor ristocetin cofactor activity and antigen.
- Published in:
- Haemophilia, 2014, v. 20, n. 1, p. 147, doi. 10.1111/hae.12264
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- Publication type:
- Article
Pregnancy complications and obstetric care in women with inherited bleeding disorders.
- Published in:
- Haemophilia, 2013, v. 19, p. 1, doi. 10.1111/hae.12269
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- Publication type:
- Article
A comparative evaluation of a new automated assay for von Willebrand factor activity.
- Published in:
- Haemophilia, 2013, v. 19, n. 2, p. 338, doi. 10.1111/hae.12064
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- Publication type:
- Article
Polymorphic mi RNA-mediated gene contribution to inhibitor development in haemophilia A.
- Published in:
- Haemophilia, 2012, v. 18, n. 6, p. 1003, doi. 10.1111/j.1365-2516.2012.02882.x
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- Publication type:
- Article
Management of bleeding disorders in adults.
- Published in:
- Haemophilia, 2012, v. 18, p. 24, doi. 10.1111/j.1365-2516.2012.02797.x
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- Publication type:
- Article
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency.
- Published in:
- Haemophilia, 2012, v. 18, n. 2, p. 205, doi. 10.1111/j.1365-2516.2011.02621.x
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- Publication type:
- Article
Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in Iran.
- Published in:
- Haemophilia, 2012, v. 18, n. 2, p. 211, doi. 10.1111/j.1365-2516.2011.02635.x
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- Publication type:
- Article
Central nervous system bleeding in patients with rare bleeding disorders.
- Published in:
- Haemophilia, 2012, v. 18, n. 1, p. 34, doi. 10.1111/j.1365-2516.2011.02545.x
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- Publication type:
- Article
Non-invasive tool for foetal sex determination in early gestational age.
- Published in:
- Haemophilia, 2011, v. 17, n. 6, p. 952, doi. 10.1111/j.1365-2516.2011.02537.x
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- Publication type:
- Article
The correlation between gene mutations and inhibitor development in patients with haemophilia A in southern Iran.
- Published in:
- Haemophilia, 2011, v. 17, n. 5, p. 820, doi. 10.1111/j.1365-2516.2011.02510.x
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- Publication type:
- Article