Works by Makris, M.
Results: 171
Recombinant factor VIIa for unlicensed indications--a definite No or a cautious Maybe in selected patients?
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- 2010
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- Publication type:
- Editorial
MECHANISTIC ENZYMOLOGY OF OXYGEN ACTIVATION BY THE CYTOCHROMES P450.
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- Drug Metabolism Reviews, 2002, v. 34, n. 4, p. 691, doi. 10.1081/DMR-120015691
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- Article
Treatment of bleeding episodes in haemophilia A complicated by a factor VIII inhibitor in patients receiving Emicizumab. Interim guidance from UKHCDO Inhibitor Working Party and Executive Committee.
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- Haemophilia, 2018, v. 24, n. 3, p. 344, doi. 10.1111/hae.13495
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- Publication type:
- Article
A golden age for Haemophilia treatment?
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- 2018
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- Publication type:
- Editorial
Pharmacokinetics, safety and efficacy of a recombinant factor IX product, trenonacog alfa in previously treated haemophilia B patients.
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- Haemophilia, 2018, v. 24, n. 1, p. 104, doi. 10.1111/hae.13324
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- Article
Haemophilia of the third age.
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- Haemophilia, 2018, v. 24, n. 1, p. 15, doi. 10.1111/hae.13257
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- Article
The coagulation laboratory monitoring of Afstyla single-chain FVIII concentrate.
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- Haemophilia, 2017, v. 23, n. 5, p. e469, doi. 10.1111/hae.13290
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- Article
First-line immune tolerance induction for children with severe haemophilia A: A protocol from the UK Haemophilia Centre Doctors' Organisation Inhibitor and Paediatric Working Parties.
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- Haemophilia, 2017, v. 23, n. 5, p. 654, doi. 10.1111/hae.13264
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- Article
von Willebrand disease and extra-intestinal angiodysplasia.
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- Haemophilia, 2017, v. 23, n. 4, p. e354, doi. 10.1111/hae.13204
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- Article
SIPPET trial: the answers.
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- 2017
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- Publication type:
- Editorial
Hepatitis C in haemophilia: time for treatment for all.
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- 2017
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- Publication type:
- Editorial
Natural history and clinical characteristics of inhibitors in previously treated haemophilia A patients: a case series.
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- Haemophilia, 2017, v. 23, n. 2, p. 255, doi. 10.1111/hae.13167
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- Article
New Findings on Inhibitor Development: from Registries to Clinical Studies.
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- Haemophilia, 2017, v. 23, p. 4, doi. 10.1111/hae.13137
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- Article
Inhibitor development in haemophilia.
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- Haemophilia, 2017, v. 23, p. 3, doi. 10.1111/hae.13145
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- Article
Factor VIII assay variability in postinfusion samples containing full length and B-domain deleted FVIII.
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- Haemophilia, 2016, v. 22, n. 5, p. 806, doi. 10.1111/hae.12962
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- Article
NHF-McMaster Guideline on Care Models for Haemophilia Management.
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- Haemophilia, 2016, v. 22, p. 6, doi. 10.1111/hae.13008
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- Article
Care models in the management of haemophilia: a systematic review.
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- Haemophilia, 2016, v. 22, p. 31, doi. 10.1111/hae.13000
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- Article
Congenital macrothrombocytopenia is a heterogeneous disorder in India.
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- Haemophilia, 2016, v. 22, n. 4, p. 570, doi. 10.1111/hae.12917
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- Article
Choosing and using non-steroidal anti-inflammatory drugs in haemophilia.
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- Haemophilia, 2016, v. 22, n. 2, p. 179, doi. 10.1111/hae.12805
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- Article
Von Willebrand factor activity assay errors.
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- Haemophilia, 2016, v. 22, n. 1, p. e74, doi. 10.1111/hae.12862
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- Article
FVIII inhibitor development according to concentrate: data from the EUHASS registry excluding overlap with other studies.
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- Haemophilia, 2016, v. 22, n. 1, p. e36, doi. 10.1111/hae.12764
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- Article
The natural history of occult or angiodysplastic gastrointestinal bleeding in von Willebrand disease.
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- Haemophilia, 2015, v. 21, n. 3, p. 338, doi. 10.1111/hae.12571
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- Article
FXI concentrate use and risk of thrombosis.
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- Haemophilia, 2014, v. 20, n. 4, p. e349, doi. 10.1111/hae.12457
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- Article
Major surgery in severe haemophilia A with inhibitors using a recombinant factor VIIa and activated prothrombin complex concentrate hybrid regimen.
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- Haemophilia, 2014, v. 20, n. 4, p. 587, doi. 10.1111/hae.12365
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- Article
Enhancing haemophilia care through registries.
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- Haemophilia, 2014, v. 20, p. 121, doi. 10.1111/hae.12406
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- Article
Enhancing haemophilia care through registries.
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- Haemophilia, 2014, v. 20, p. 121, doi. 10.1111/hae.12406
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- Article
Assaying FVIII activity: one method is not enough, and never was.
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- 2014
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- Publication type:
- Editorial
Switching clotting factor concentrates: considerations in estimating the risk of immunogenicity.
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- Haemophilia, 2014, v. 20, n. 2, p. 200, doi. 10.1111/hae.12283
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- Article
Update to UKHCDO guidance on vaccination against hepatitis A and B viruses in patients with inherited coagulation factor deficiencies and von Willebrand disease.
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- Haemophilia, 2013, v. 19, n. 3, p. e191, doi. 10.1111/hae.12139
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- Article
Third Åland islands conference on von Willebrand disease, 26-28 September 2012: meeting report.
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- Haemophilia, 2013, v. 19, p. 1, doi. 10.1111/hae.12078
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- Article
Prophylaxis in severe forms of von Willebrand's disease: results from the von Willebrand Disease Prophylaxis Network (VWD PN).
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- Haemophilia, 2013, v. 19, n. 1, p. 76, doi. 10.1111/j.1365-2516.2012.02916.x
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- Article
The World Federation of Hemophilia guideline on management of haemophilia.
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- Haemophilia, 2013, v. 19, n. 1, p. 1, doi. 10.1111/hae.12074
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- Article
Pharmacokinetic properties of IB1001, an investigational recombinant factor IX, in patients with haemophilia B: repeat pharmacokinetic evaluation and sialylation analysis.
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- Haemophilia, 2012, v. 18, n. 6, p. 881, doi. 10.1111/j.1365-2516.2012.02897.x
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- Article
Malignant disease in the haemophilic population: moving towards a management consensus?
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- Haemophilia, 2012, v. 18, n. 5, p. 664, doi. 10.1111/j.1365-2516.2012.02846.x
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- Article
How I treat inhibitors in haemophilia.
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- Haemophilia, 2012, v. 18, p. 48, doi. 10.1111/j.1365-2516.2012.02829.x
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- Article
A prospective registry of European haemophilia B patients receiving nonacog alfa, recombinant human factor IX, for usual use.
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- Haemophilia, 2012, v. 18, n. 4, p. 503, doi. 10.1111/j.1365-2516.2011.02685.x
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- Article
Management of muscle haematomas in patients with severe haemophilia in an evidence-poor world.
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- Haemophilia, 2012, v. 18, n. 4, p. 598, doi. 10.1111/j.1365-2516.2011.02720.x
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- Article
Thrombotic adverse events to coagulation factor concentrates for treatment of patients with haemophilia and von Willebrand disease: a systematic review of prospective studies.
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- Haemophilia, 2012, v. 18, n. 3, p. e173, doi. 10.1111/j.1365-2516.2012.02758.x
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- Article
Non-thrombotic-, non-inhibitor-associated adverse reactions to coagulation factor concentrates for treatment of patients with hemophilia and von Willebrand's disease: a systematic review of prospective studies.
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- Haemophilia, 2012, v. 18, n. 3, p. e164, doi. 10.1111/j.1365-2516.2011.02745.x
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- Article
The risk of variant Creutzfeldt-Jakob disease among UK patients with bleeding disorders, known to have received potentially contaminated plasma products.
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- Haemophilia, 2011, v. 17, n. 6, p. 931, doi. 10.1111/j.1365-2516.2011.02508.x
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- Article
UKHCDO guidelines on the management of HCV in patients with hereditary bleeding disorders 2011.
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- Haemophilia, 2011, v. 17, n. 5, p. e877, doi. 10.1111/j.1365-2516.2011.02585.x
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- Article
Experience with Optivate.
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- Haemophilia, 2011, v. 17, n. 3, p. 428, doi. 10.1111/j.1365-2516.2010.02441.x
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- Article
Pharmacokinetics of Optivate.
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- Haemophilia, 2011, v. 17, n. 2, p. 185, doi. 10.1111/j.1365-2516.2010.02414.x
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- Article
Clinical assessment of Optivate.
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- Haemophilia, 2011, v. 17, n. 3, p. 456, doi. 10.1111/j.1365-2516.2010.02446.x
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- Article
Biovigilance and pharmacovigilance for haemophilia.
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- Haemophilia, 2010, v. 16, p. 17, doi. 10.1111/j.1365-2516.2010.02288.x
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- Article
Risk reduction strategies for variant Creutzfeldt–Jakob disease transmission by UK plasma products and their impact on patients with inherited bleeding disorders.
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- Haemophilia, 2010, v. 16, n. 2, p. 305, doi. 10.1111/j.1365-2516.2010.02220.x
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- Article
Guideline on the selection and use of therapeutic products to treat haemophilia and other hereditary bleeding disorders.
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- Haemophilia, 2008, v. 14, n. 4, p. 671, doi. 10.1111/j.1365-2516.2008.01695.x
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- Article
Paracetamol/acetaminophen usage in haemophilia: more caution needed?
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- Haemophilia, 2008, v. 14, n. 3, p. 434, doi. 10.1111/j.1365-2516.2008.01653.x
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- Article
Liver transplantation for factor XI deficiency: cure before diagnosis.
- Published in:
- 2008
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- Publication type:
- Letter
Haemoperitoneum associated with ovulation in women with bleeding disorders: the case for conservative management and the role of the contraceptive pill.
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- Haemophilia, 2007, v. 13, n. 1, p. 93, doi. 10.1111/j.1365-2516.2006.01399.x
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- Publication type:
- Article