Works matching DE "VON Willebrand disease"
Results: 1609
Use of routine histopathology and factor VIII-related antigen/von Willebrand factor immunohistochemistry to differentiate primary hemangiosarcoma of bone from telangiectatic osteosarcoma in 54 dogs.
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- Veterinary & Comparative Oncology, 2017, v. 15, n. 4, p. 1232, doi. 10.1111/vco.12259
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Canine mammary carcinomas: influence of histological grade, vascular invasion, proliferation, microvessel density and VEGFR2 expression on lymph node status and survival time.
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- Veterinary & Comparative Oncology, 2017, v. 15, n. 2, p. 450, doi. 10.1111/vco.12189
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Impact of von Willebrand Disease on Women's Health Outcomes: A Matched Cohort Database Study.
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- Journal of Women's Health (15409996), 2022, v. 31, n. 9, p. 1262, doi. 10.1089/jwh.2022.0082
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Bleeding Disorders in Women and Girls: State of the Science and CDC Collaborative Programs.
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- Journal of Women's Health (15409996), 2022, v. 31, n. 3, p. 301, doi. 10.1089/jwh.2022.0008
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Factoring Them In: Shining the Spotlight on Women and Girls with Congenital Bleeding Disorders.
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- Journal of Women's Health (15409996), 2020, v. 29, n. 5, p. 608, doi. 10.1089/jwh.2019.8255
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A Cross-Sectional Study of Women and Girls with Congenital Bleeding Disorders: The American Thrombosis and Hemostasis Network Cohort.
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- Journal of Women's Health (15409996), 2020, v. 29, n. 5, p. 670, doi. 10.1089/jwh.2019.7930
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Chemie für alle: ein Plädoyer für Chancengleichheit.
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- Angewandte Chemie, 2019, v. 131, n. 10, p. 2936, doi. 10.1002/ange.201901594
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Recombinant factor VIIa use in patients with the rarest forms of inherited coagulation-factor deficiencies: a study of cases from the www.haemostasis.com registry.
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- Comparative Clinical Pathology, 2006, v. 15, n. 4, p. 203, doi. 10.1007/s00580-006-0645-z
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Safety and oncological outcome following radiofrequency ablation of small renal masses in a single center.
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- Scandinavian Journal of Urology, 2021, v. 55, n. 3, p. 203, doi. 10.1080/21681805.2021.1900386
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Gastroduodenal Obstruction Secondary to Pica-associated Bezoar: A Case Report.
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- Clinical Practice & Cases in Emergency Medicine, 2025, v. 9, n. 1, p. 53, doi. 10.5811/cpcem.21300
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Multicenter retrospective study of transcatheter arterial embolisation for life-threatening haemorrhage in patients with uncorrected bleeding diathesis.
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- CVIR Endovascular, 2020, v. 3, n. 1, p. 1, doi. 10.1186/s42155-020-00186-3
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Anesthesia management for emergency cesarean section in a patient affected by von Willebrand's disease with perinatal distress.
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- Pediatric Anesthesia & Critical Care Journal (PACCJ), 2013, v. 1, n. 1, p. 39, doi. 10.14587/paccj.2013.8
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Study of etipoathogenesis of different forms of epistaxis: Observational study.
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- Indian Journal of Basic & Applied Medical Research, 2021, v. 10, p. 9, doi. 10.36848/IJBAMR/2020/30215.5560
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Administration of plasma-derived coagulation factor VIII during the perioperative period of mastectomy for breast cancer with acquired von Willebrand syndrome.
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- Surgical Case Reports, 2018, v. 4, n. 1, p. 1, doi. 10.1186/s40792-018-0528-y
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Assessment of Endothelial Dysfunction by Measuring Von Willebrand Factor and Exhaled Nitric Oxide in Patients with Chronic Obstructive Pulmonary Disease.
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- Collegium Antropologicum, 2013, v. 37, n. 4, p. 1153
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VON WILLEBRAND FACTOR LEVEL IN PATIENTS WITH ATHEROTHROMBOTIC ISCHEMIC STROKE AND CARDIOEMBOLIC ISCHEMIC STROKE WITH ATRIAL FIBRILLATION.
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- Bulletin of Taras Shevchenko National University of Kyiv / Vestnik Kievskogo Nacional'Nogo Universiteta Imeni Tarasa Ševčenko, 2014, v. 66, n. 1, p. 55
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FACTOR-X DEFICIENCY: A RARE DISORDER TO BE LOOKED FOR IN CASES OF CONGENITAL BLEEDING TENDENCY.
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- Khyber Medical University Journal, 2018, v. 10, n. 3, p. 163, doi. 10.35845/kmuj.2018.18270
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Acquired Von Willebrand Syndrome and Blood Pump Design.
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- Artificial Organs, 2018, v. 42, n. 12, p. 1119, doi. 10.1111/aor.13291
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Influence of a Rotational Speed Modulation System Used With an Implantable Continuous-Flow Left Ventricular Assist Device on von Willebrand Factor Dynamics.
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- Artificial Organs, 2016, v. 40, n. 9, p. 877, doi. 10.1111/aor.12666
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Preclinical Models for Translational Investigations of Left Ventricular Assist Device-Associated von Willebrand Factor Degradation.
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- Artificial Organs, 2015, v. 39, n. 7, p. 1, doi. 10.1111/aor.12428
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Establishing a Method for In Vitro Investigation of Mechanical Parameters Causing Acquired von Willebrand Syndrome in Ventricular Assist Devices.
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- Artificial Organs, 2013, v. 37, n. 9, p. 833, doi. 10.1111/aor.12116
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Genetically determined telomere length and risk for haematologic diseases: results from large prospective cohorts and Mendelian Randomization analysis.
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- Blood Cancer Journal, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41408-024-01035-5
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Comprehensive Analyses of Coagulation Parameters in Patients with Vascular Anomalies.
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- Biomolecules (2218-273X), 2022, v. 12, n. 12, p. 1840, doi. 10.3390/biom12121840
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A core outcome set for prophylaxis and perioperative treatment of von Willebrand disease: The coreVWD initiative.
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- Haemophilia, 2024, v. 30, n. 6, p. 1357, doi. 10.1111/hae.15122
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Patient‐reported data on the severity of Von Willebrand disease.
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- Haemophilia, 2024, v. 30, n. 6, p. 1348, doi. 10.1111/hae.15103
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Efficacy and safety of a recombinant von Willebrand factor treatment in acquired von Willebrand syndrome in case of bleeding and surgical procedures.
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- Haemophilia, 2024, v. 30, n. 6, p. 1341, doi. 10.1111/hae.15098
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Efficacy of a 1:1 ratio VWF/FVIII concentrate in patients with von Willebrand disease.
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- Haemophilia, 2024, v. 30, n. 5, p. 1148, doi. 10.1111/hae.15079
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A case of bruising and joint hypermobility: The need to consider genetic testing for platelet disorders.
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- Haemophilia, 2024, v. 30, n. 5, p. 1225, doi. 10.1111/hae.15066
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Review of interventions and effectiveness for heavy menstrual bleeding in women with moderate and severe von Willebrand disease.
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- Haemophilia, 2024, v. 30, n. 5, p. 1177, doi. 10.1111/hae.15078
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Low bleeding rates after intramuscular Covid‐19 vaccination in patients with haemophilia and von Willebrand disease: Outcome data from the Swedish haemophilia registry.
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- Haemophilia, 2024, v. 30, n. 5, p. 1217, doi. 10.1111/hae.15063
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Limited value of testing for factor XIII and α2‐antiplasmin deficiency in patients with a bleeding disorder of unknown cause.
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- Haemophilia, 2024, v. 30, n. 4, p. 998, doi. 10.1111/hae.15059
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Oral surgery in people with inherited bleeding disorder: A retrospective study.
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- Haemophilia, 2024, v. 30, n. 4, p. 943, doi. 10.1111/hae.15055
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Alleviated bleeding phenotypes in a child with severe haemophilia A and thalassemia disease.
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- Haemophilia, 2024, v. 30, n. 4, p. 1092, doi. 10.1111/hae.15041
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Retrospective chart review of GI bleeding in people with von Willebrand disease.
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- Haemophilia, 2024, v. 30, n. 4, p. 970, doi. 10.1111/hae.15034
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Spectrum, clinical characteristics and outcome of von Willebrand disease in Oman.
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- Haemophilia, 2024, v. 30, n. 4, p. 1080, doi. 10.1111/hae.15029
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Dental management of people with complex or rare inherited bleeding disorders.
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- Haemophilia, 2024, v. 30, p. 128, doi. 10.1111/hae.15005
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Diagnosis and treatment of von Willebrand disease in 2024 and beyond.
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- Haemophilia, 2024, v. 30, p. 103, doi. 10.1111/hae.14970
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Diagnosis and treatment challenges in lower resource countries: State‐of‐the‐art.
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- Haemophilia, 2024, v. 30, p. 78, doi. 10.1111/hae.14956
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Targeting a higher plasma VWF level at time of delivery in pregnant individuals with von Willebrand disease: Outcomes at a single‐institution cohort study.
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- Haemophilia, 2024, v. 30, n. 2, p. 470, doi. 10.1111/hae.14953
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Adult haematology clinics for menstruating/pregnant patients: A single center experience and lessons learned: Haematology/Gynaecology Clinics for Adults.
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- Haemophilia, 2024, v. 30, n. 2, p. 564, doi. 10.1111/hae.14950
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Impact of inherited bleeding disorders on maternal bleeding and other pregnancy outcomes: A population‐based cohort study.
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- Haemophilia, 2024, v. 30, n. 2, p. 478, doi. 10.1111/hae.14922
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Poster Abstracts.
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- Haemophilia, 2024, v. 30, p. 34, doi. 10.1111/hae.14919
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Main Congress Oral Abstracts.
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- Haemophilia, 2024, v. 30, p. 18, doi. 10.1111/hae.14916
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Speaker Abstracts.
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- Haemophilia, 2024, v. 30, p. 5, doi. 10.1111/hae.14915
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Von Willebrand Factor (VWF) multiplex activity assay differentiation of type 1 von Willebrand Disease (VWD) and variant VWD.
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- Haemophilia, 2024, v. 30, n. 1, p. 161, doi. 10.1111/hae.14901
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Direct data transfer of people with hereditary bleeding disorders from the Thai haemophilia treatment centre registry to the Annual Global Survey of the World Federation of Hemophilia.
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- Haemophilia, 2024, v. 30, n. 1, p. 245, doi. 10.1111/hae.14897
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In vitro field study and worldwide survey assessing how clinical haemostasis laboratories analyse recombinant and plasma‐derived von Willebrand factor products.
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- Haemophilia, 2024, v. 30, n. 1, p. 151, doi. 10.1111/hae.14892
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An open‐label, multi‐centre, post‐marketing study to assess the efficacy and safety of a plasma‐derived VWF/FVIII concentrate in patients with von Willebrand disease.
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- Haemophilia, 2024, v. 30, n. 1, p. 236, doi. 10.1111/hae.14868
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Preclinical development and characterization of a human plasma‐derived high‐purity factor X concentrate for therapeutic use.
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- Haemophilia, 2023, v. 29, n. 6, p. 1394, doi. 10.1111/hae.14875
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The World Health Organisation's list of essential medicines and haemophilia treatment products.
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- Haemophilia, 2023, v. 29, n. 6, p. 1387, doi. 10.1111/hae.14879
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