Works matching IS 13518216 AND DT 2020 AND VI 26
Results: 254
Determining meaningful health‐related quality‐of‐life improvement in persons with haemophilia A using the Haemophilia Quality of Life Questionnaire for Adults (Haem‐A‐QoL).
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- Haemophilia, 2020, v. 26, n. 6, p. 1019, doi. 10.1111/hae.14184
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Patient satisfaction with US Hemophilia Treatment Center Care, Teams and Services: The First National Survey.
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- Haemophilia, 2020, v. 26, n. 6, p. 991, doi. 10.1111/hae.14176
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Evaluating international Haemophilia Joint Health Score (HJHS) results combined with expert opinion: Options for a shorter HJHS.
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- Haemophilia, 2020, v. 26, n. 6, p. 1072, doi. 10.1111/hae.14180
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The challenge of genetically unresolved haemophilia A patients: Interest of the combination of whole F8 gene sequencing and functional assays.
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- Haemophilia, 2020, v. 26, n. 6, p. 1056, doi. 10.1111/hae.14179
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Quality of electronic treatment records and adherence to prophylaxis in haemophilia and von Willebrand disease: Systematic assessments from an electronic diary.
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- Haemophilia, 2020, v. 26, n. 6, p. 999, doi. 10.1111/hae.14178
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Effects of Emicizumab on APTT, FVIII assays and FVIII Inhibitor assays using different reagents: Results of a UK NEQAS proficiency testing exercise.
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- Haemophilia, 2020, v. 26, n. 6, p. 1087, doi. 10.1111/hae.14177
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Health‐related quality of life and caregiver burden of emicizumab in children with haemophilia A and factor VIII inhibitors—Results from the HAVEN 2 study.
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- Haemophilia, 2020, v. 26, n. 6, p. 1009, doi. 10.1111/hae.14183
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Bleeding of unknown cause and unclassified bleeding disorders; diagnosis, pathophysiology and management.
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- Haemophilia, 2020, v. 26, n. 6, p. 946, doi. 10.1111/hae.14174
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Management of patients with severe haemophilia a without inhibitors on prophylaxis with emicizumab: AICE recommendations with focus on emergency in collaboration with SIBioC, SIMEU, SIMEUP, SIPMeL and SISET.
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- Haemophilia, 2020, v. 26, n. 6, p. 937, doi. 10.1111/hae.14172
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Cross‐reacting recombinant porcine FVIII inhibitors in patients with acquired haemophilia A.
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- Haemophilia, 2020, v. 26, n. 6, p. 1181, doi. 10.1111/hae.14162
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Low rate of subclinical venous thrombosis in patients with haemophilia undergoing major orthopaedic surgery in the absence of pharmacological thromboprophylaxis.
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- Haemophilia, 2020, v. 26, n. 6, p. 1064, doi. 10.1111/hae.14161
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Telehealth for delivery of haemophilia comprehensive care during the COVID‐19 pandemic.
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- Haemophilia, 2020, v. 26, n. 6, p. 984, doi. 10.1111/hae.14156
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3D gait analysis, haemophilia joint health score, leg muscle laterality and biomarkers of joint damage: A cross‐sectional comparative assessment of haemophilic arthropathy.
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- Haemophilia, 2020, v. 26, n. 6, p. e323, doi. 10.1111/hae.14154
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Real‐world data demonstrate improved bleed control and extended dosing intervals for patients with haemophilia B after switching to recombinant factor IX Fc fusion protein (rFIXFc) for up to 5 years.
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- Haemophilia, 2020, v. 26, n. 6, p. 975, doi. 10.1111/hae.14152
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Acupuncture as a therapeutic resource for treatment of chronic pain in people with haemophilia.
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- Haemophilia, 2020, v. 26, n. 6, p. e315, doi. 10.1111/hae.14151
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Treatment of pelvic haemophilic pseudotumour: A retrospective study.
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- Haemophilia, 2020, v. 26, n. 6, p. e308, doi. 10.1111/hae.14148
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Challenges and key lessons from the design and implementation of an international haemophilia registry supported by a pharmaceutical company.
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- Haemophilia, 2020, v. 26, n. 6, p. 966, doi. 10.1111/hae.14144
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National registry of haemophilia and other coagulopathies: A multisector initiative in the Colombian Health System.
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- Haemophilia, 2020, v. 26, n. 6, p. e254, doi. 10.1111/hae.14138
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Patient and caregiver preferences for haemophilia A treatments: A discrete choice experiment.
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- Haemophilia, 2020, v. 26, n. 6, p. e291, doi. 10.1111/hae.14137
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Primary prophylaxis was associated with lower arthropathy in Colombian men with haemophilia B: A longitudinal analysis (2015‐2019).
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- Haemophilia, 2020, v. 26, n. 6, p. e282, doi. 10.1111/hae.14136
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Initiation of emicizumab prophylaxis in an infant with haemophilia A and subdural haemorrhage.
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- Haemophilia, 2020, v. 26, n. 6, p. e353, doi. 10.1111/hae.14133
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Management of previously untreated patients with severe haemophilia A preferentially treated with recombinant factor VIII products: Two French centres' real‐life experience.
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- Haemophilia, 2020, v. 26, n. 6, p. e349, doi. 10.1111/hae.14132
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Gene therapy to cure haemophilia: Is robust scientific inquiry the missing factor?
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- Haemophilia, 2020, v. 26, n. 6, p. 931, doi. 10.1111/hae.14131
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Impact of COVID‐19 pandemic on mental health of patients with inherited bleeding disorders in Germany.
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- Haemophilia, 2020, v. 26, n. 6, p. e272, doi. 10.1111/hae.14130
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Weather changes leading to bleeding in arthropathic joints among individuals with haemophilia: Symptoms of meteoropathy?
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- Haemophilia, 2020, v. 26, n. 6, p. e346, doi. 10.1111/hae.14126
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Arthroplasty in haemophilia: Double‐edged sword in low/middle‐income countries.
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- Haemophilia, 2020, v. 26, n. 6, p. e344, doi. 10.1111/hae.14124
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Emerging benefits of Fc fusion technology in the context of recombinant factor VIII replacement therapy.
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- Haemophilia, 2020, v. 26, n. 6, p. 958, doi. 10.1111/hae.14123
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Bleeding complications during pregnancy and delivery in haemophilia carriers and their neonates in Western France: An observational study.
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- Haemophilia, 2020, v. 26, n. 6, p. 1046, doi. 10.1111/hae.14117
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Case report of a fatal rectal haemorrhage in a person with severe haemophilia A receiving emicizumab and high‐dose bypassing agents in the HAVEN 1 study.
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- Haemophilia, 2020, v. 26, n. 6, p. e340, doi. 10.1111/hae.14110
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Management of haemophilia patients in the COVID‐19 pandemic: Experience in Wuhan and Tianjin, two differently affected cities in China.
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- Haemophilia, 2020, v. 26, n. 6, p. 1031, doi. 10.1111/hae.14108
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Acquired haemophilia A after alemtuzumab therapy.
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- Haemophilia, 2020, v. 26, n. 6, p. e337, doi. 10.1111/hae.14107
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Optimal trough levels in haemophilia B: Raising expectations.
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- Haemophilia, 2020, v. 26, n. 6, p. e334, doi. 10.1111/hae.14098
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Portal vein thrombosis in a patient known for congenital afibrinogenemia.
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- Haemophilia, 2020, v. 26, n. 6, p. e331, doi. 10.1111/hae.14092
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Clinical utility of sample preheat treatment in a modified Nijmegen‐Bethesda assay (mNBA) for inhibitor monitoring in congenital and acquired haemophilia A: A single‐centre four‐year experience.
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- Haemophilia, 2020, v. 26, n. 6, p. e300, doi. 10.1111/hae.14090
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Effect of emicizumab on thrombin generation: A case report of breakthrough bleeding during emicizumab treatment.
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- Haemophilia, 2020, v. 26, n. 6, p. e327, doi. 10.1111/hae.14085
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Long‐term safety and sustained efficacy for up to 5 years of treatment with recombinant factor IX Fc fusion protein in subjects with haemophilia B: Results from the B‐YOND extension study.
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- Haemophilia, 2020, v. 26, n. 6, p. e262, doi. 10.1111/hae.14036
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A neonate bearing a novel genetic variant within the factor XIII active site presenting with severe umbilical haemorrhage.
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- Haemophilia, 2020, v. 26, n. 6, p. e324, doi. 10.1111/hae.14074
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An international survey to evaluate systemic bevacizumab for chronic bleeding in hereditary haemorrhagic telangiectasia.
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- Haemophilia, 2020, v. 26, n. 6, p. 1038, doi. 10.1111/hae.14034
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Adherence is a human behaviour, assessing it requires multimethod evaluation with validated measures: Comment on Guedes VG et al (2019).
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- Haemophilia, 2020, v. 26, n. 6, p. 934, doi. 10.1111/hae.14022
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Issue Information.
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- Haemophilia, 2020, v. 26, n. 6, p. 925, doi. 10.1111/hae.13798
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Growing success and ambitions of the Chinese edition of Haemophilia.
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- Haemophilia, 2020, v. 26, n. 5, p. 750, doi. 10.1111/hae.14164
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Identification of new F8 deep intronic variations in patients with haemophilia A.
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- Haemophilia, 2020, v. 26, n. 5, p. 847, doi. 10.1111/hae.14134
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Paediatric patients with blood‐induced ankle joint arthritis demonstrate physiological foot joint mechanics and energetics during walking.
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- Haemophilia, 2020, v. 26, n. 5, p. 907, doi. 10.1111/hae.14128
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Low bone mass and hypovitaminosis D in haemophilia: A single‐centre study in patients with severe and moderate haemophilia A and B.
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- Haemophilia, 2020, v. 26, n. 5, p. 898, doi. 10.1111/hae.14127
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Haemostatic efficacy of single‐dose factor administration in neonates with severe haemophilia undergoing circumcision.
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- Haemophilia, 2020, v. 26, n. 5, p. 786, doi. 10.1111/hae.14122
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Illness cognitions associated with health‐related quality of life in young adult men with haemophilia.
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- Haemophilia, 2020, v. 26, n. 5, p. 793, doi. 10.1111/hae.14120
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Comparing clotting factors attributes across different methods of preference elicitation in haemophilia patients.
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- Haemophilia, 2020, v. 26, n. 5, p. 817, doi. 10.1111/hae.14119
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Complications of total knee arthroplasty in patients with haemophilia compared with osteoarthritis and rheumatoid arthritis: A 20‐year single‐surgeon cohort.
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- Haemophilia, 2020, v. 26, n. 5, p. 861, doi. 10.1111/hae.14115
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Joint health and treatment modalities in Nordic patients with moderate haemophilia A and B – The MoHem study.
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- Haemophilia, 2020, v. 26, n. 5, p. 891, doi. 10.1111/hae.14114
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Early wound complications after orthopaedic surgery for haemophilia: What can we do more.
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- Haemophilia, 2020, v. 26, n. 5, p. 882, doi. 10.1111/hae.14113
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