Results 41 to 50 of about 12,413,959 (307)
Medicina, 2021 We present the case of a 70-year-old man with a history of haemophilia B, who presented to our hospital with a non-ST-elevation myocardial infarction.
Konstantinos C. Theodoropoulos +6 more
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Haemophilia A and haemophilia B: molecular insights [PDF]
Molecular Pathology, 2002 This review focuses on selected areas that should interest both the scientist and the clinician alike: polymorphisms within the factor VIII and factor IX genes, their linkage, and their ethnic variation; a general assessment of mutations within both genes and a detailed inspection of the molecular pathology of certain mutations to illustrate the ...
openaire +4 more sources
Clinical profile of children with haemophilia at the University Hospital of Brazzaville
The Journal of Haemophilia Practice, 2020 Haemophilia is a rare hereditary haemorrhagic disease caused by coagulation factor VIII (haemophilia A) or IX (haemophilia B) deficiency. Very few data exist on this disease in Congo.
Galiba Atipo Tsiba FO +5 more
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BMJ Open, 2021 Introduction Two meta-analyses showed lower bone mineral density (BMD) in patients with haemophilia (haemophilia type and severity were often not specified) compared with healthy controls.
Brigitte Tardy‐Poncet +7 more
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The use of rIX-FP in patients with haemophilia B: a nurse's perspective
The Journal of Haemophilia Practice, 2021 The management of patients with haemophilia is complex and requires lifelong care to be delivered by a specialist multidisciplinary team. Haemophilia B results from a deficiency or absence in coagulation factor IX (FIX), leading to easy bruising, and ...
Garner Kara +2 more
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Plasma levels of IL-1β and IL-37 in patients with severe haemophilia
Journal of International Medical Research, 2020 Objective Haemophilia A and B are disorders caused by the lack of clotting factors VIII and IX, respectively. Repeated bleeding into the same joint leads to haemophilic arthropathy (HA).
Pei-Chin Lin +7 more
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The Journal of Haemophilia Practice, 2022 Haemophilia is an inherited X-linked bleeding disorder characterised by a deficiency or absence of clotting factor VIII (haemophilia A) or IX (haemophilia B), which can cause musculoskeletal bleeding. The standard treatment for haemophilia is with factor
Das Arijit +3 more
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Hematology, 2023 Background and Objectives Haemophilia comprises a continuum of blood disorders that often include joint and muscular dysfunction, which may lead to a constellation of activity limitations and participation restrictions.
Bao-Feng Geng +4 more
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Orphanet Journal of Rare Diseases, 2022 Background Haemophilia bears substantial humanistic and economic burden on children and their caregivers. Characterising the differential impact of severe versus moderate paediatric haemophilia is important for clinical and health policy decisions.
Idaira Rodriguez-Santana +6 more
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Causes of death and mortality trends related to hemophilia in Brazil, 1999 to 2016
Hematology, Transfusion and Cell Therapy, 2021 Introduction: Multiple cause of death methodology enhances mortality studies beyond the traditional underlying cause of death approach. Aim: This study aims to describe causes of death and mortality issues related to haemophilia with the use of multiple ...
Augusto Hasiak Santo
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