Results 101 to 110 of about 118,635,816 (237)

Acquired hemophilia A in chronic lymphocytic leukemia: A case report

, 2019
0000-0003-0238-2236; 0000-0001-9178-2850WOS: 000484872100020PubMed ID: 31320278Acquired hemophilia A, due to spontaneous autoantibody against FVIII, is a rare hemorrhagic disorder with an incidence of about 1 per million population per year.
Karakuş, Volkan, Kaya, Egemen, Dere, Yelda, Kurtoğlu, Erdal   +3 more
core   +1 more source

Clinical Outcomes of Efanesoctocog Alfa Prophylaxis in Children With Severe Haemophilia A: Interim Data From XTEND‐ed

Haemophilia, EarlyView.
Lynn Malec, Beatrice Nolan, Anthony K C Chan, Manuela Albisetti, Sheng‐Chieh Chou, Bulent Zulfikar, Mindy Simpson, Liqi Feng, Helena Palmborg, Graham Neill, Lydia Abad‐Franch, Sriya Gunawardena, Karin Fijnvandraat   +12 more
wiley   +1 more source

Ultrasound Versus Magnetic Resonance Imaging for Haemophilic Arthropathy: A Systematic Review With Meta‐Analysis of Diagnostic Accuracy Across Joint Pathologies

Haemophilia, EarlyView.
ABSTRACT Introduction Haemophilic arthropathy (HA) is a debilitating consequence of recurrent intra‐articular bleeding. While magnetic resonance imaging (MRI) is the established gold standard for joint assessment, musculoskeletal ultrasound (US) has emerged as a point‐of‐care alternative.
George Triantafyllou, Konstantina Bolou, Aikaterini Michalopoulou, Athina Dettoraki, Nikolaos‐Achilleas Arkoudis, Maria Piagkou, Olympia Papakonstantinou, Helen Pergantou   +7 more
wiley   +1 more source

Hereditary and acquired hemophilia

, 2022
Danas su poznate tri vrste nasljedne hemofilije : najčešća hemofilija A, zatim hemofilija B, te vrlo rijetka hemofilija C. Ostalih 5 do 10% nasljednih koagulacijskih poremećaja uzrokuju deficiti drugih faktora koji uključuju faktor II, V,VII, X, XII i ...
Peček, Sara
core   +1 more source

A Case of Renal Pelvic Cancer with Acquired Hemophilia and Leukemoid Reaction [PDF]

, 2018
A 71-year-old man was referred to us with a right renal mass that was discovered by computed tomography (CT) examination for acquired hemophilia and leukemoid reaction.
大森, 聡, 中村, 泰行, 氏家, 隆, 五十嵐, 大樹, 阿部, 正和, 泉田, 亘, 小原, 航   +6 more
core   +1 more source

Successful eradication of acquired factor VIII inhibitors with rituximab: a report of two cases

Hematology
Objectives Acquired hemophilia A (AHA) is a rare autoimmune disorder that presents with spontaneous bleeding due to the development of autoantibodies against coagulation factor VIII.
Ma'in Abumuhfouz, Anas Al-sadi, Awni Alshurafa, Israa Jawarneh, Ruba Y. Taha, Sarah A. Elkourashy   +5 more
doaj   +1 more source

Acquired Hemophilia A successfully treated with rituximab

Mediterranean Journal of Hematology and Infectious Diseases, 2015
Acquired hemophilia A (AHA) is a rare bleeding disorder due to the development of specific autoantibodies against factor VIII. The anti-CD20 monoclonal antibody Rituximab has been proven to be effective in  obtaining a long-term suppression of inhibitors
Giovanni D'Arena, Elvira Grandone, Matteo Nicola Dario Di Minno, Pellegrino Musto, Giovanni Di Minno   +4 more
doaj   +1 more source

Efficacy of Air‐Polishing in Managing Biofilm Formation in Patients Wearing Fixed Orthodontic Appliances: A Single‐Blind, Split‐Mouth, Randomised Controlled Trial

International Journal of Dental Hygiene, EarlyView.
ABSTRACT Objectives To investigate the efficacy of air‐polishing in managing biofilm formation in patients wearing fixed orthodontic appliances. Methods This pilot study was designed as a single‐blind split‐mouth randomised controlled study. Twenty patients undergoing fixed orthodontic treatment were enrolled.
James Millar, Tianyou Wu, Richard D. Cannon, Mauro Farella, Li Mei   +4 more
wiley   +1 more source

Concomitant Acquired Hemophilia A and Acquired Von Willebrand Syndrome from Distinctive Autoantibodies: Case Report

Hematology Reports
Background and Clinical Significance: Acquired hemophilia A (AHA) and acquired von Willebrand syndrome (AVWS) are rare bleeding disorders that do not often present concurrently.
Richard Yu, Mackenzie Bowman, Arnaud Bonnefoy, Paula James, Chai W. Phua   +4 more
doaj   +1 more source

Advanced Molecular Analysis in Hemophilia A in a Single Step: Next Generation Sequencing (NGS) and Copy Number Variation (CNV) Analysis

International Journal of Laboratory Hematology, EarlyView.
ABSTRACT Background Hemophilia A, an X‐linked bleeding disorder caused by pathogenic variants in the F8 gene, requires precise genetic diagnosis for optimal management. Conventional stepwise sequence and copy number variation (CNV) analyses are time‐consuming and may leave some cases unresolved.
Enise Avci Durmusalioglu, Esra Isik, Basak Durmus Ozen, Mehmet Mert Topaloglu, Nihal Karadas, Kaan Kavakli, Melike Sezgin Evim, Tolga Aslan, Erşen Kavak, Adalet Meral Gunes, Funda Tayfun Kupesiz, Alphan Kupesiz, Fahri Sahin, Tahir Atik   +13 more
wiley   +1 more source