Found: 13
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Lack of the human choline transporter‐like protein SLC44A2 causes hearing impairment and a rare red blood phenotype.
- Published in:
- EMBO Molecular Medicine, 2023, v. 15, n. 3, p. 1, doi. 10.15252/emmm.202216320
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- Publication type:
- Article
Apheresis Efficacy and Tolerance in the Setting of HLA-Incompatible Kidney Transplantation.
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- Journal of Clinical Medicine, 2021, v. 10, n. 6, p. 1316, doi. 10.3390/jcm10061316
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- Publication type:
- Article
How to improve clotting factors depletion in double‐filtration plasmapheresis.
- Published in:
- Journal of Clinical Apheresis, 2021, v. 36, n. 5, p. 766, doi. 10.1002/jca.21928
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- Publication type:
- Article
Fibrinogen reconstitution after therapeutic apheresis: Comparison of double‐filtration plasmapheresis, plasma exchange, and immunoadsorption.
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- Journal of Clinical Apheresis, 2021, v. 36, n. 4, p. 574, doi. 10.1002/jca.21895
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- Publication type:
- Article
Comparison of three modalities of plasmapheresis on coagulation: Centrifugal, single‐membrane filtration, and double‐filtration plasmapheresis.
- Published in:
- Journal of Clinical Apheresis, 2021, v. 36, n. 3, p. 408, doi. 10.1002/jca.21879
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- Publication type:
- Article
Effect of immunoadsorption alone or combined with membrane filtration on hemostasis parameters.
- Published in:
- Journal of Clinical Apheresis, 2020, v. 35, n. 5, p. 444, doi. 10.1002/jca.21825
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- Publication type:
- Article
Cerebral Venous Thrombosis: Clinical, Radiological, Biological, and Etiological Characteristics of a French Prospective Cohort (FPCCVT)—Comparison With ISCVT Cohort.
- Published in:
- Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.753110
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- Publication type:
- Article
Are coagulation profiles in Andean highlanders with excessive erythrocytosis favouring hypercoagulability?
- Published in:
- Experimental Physiology, 2024, v. 109, n. 6, p. 899, doi. 10.1113/EP091670
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- Publication type:
- Article
The administration of four-factor prothrombin complex concentrate exacerbates thrombin generation in trauma patients at risk of massive transfusion: an ancillary study of the PROCOAG trial.
- Published in:
- 2024
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- Publication type:
- Letter
Plasminogen gene mutation with normal C1 inhibitor hereditary angioedema: Three additional French families.
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- 2018
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- Publication type:
- Letter to the Editor
Multicentre evaluation of CK Prest<sup>®</sup> for assaying plasma levels of factor IX fused with albumin (Idelvion<sup>®</sup>).
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. e327, doi. 10.1111/hae.13812
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- Publication type:
- Article
Reducing Fibrinogen and Factor XIII Using Double-Filtration Plasmapheresis for Antibody-Mediated Rejection: Predictive Models.
- Published in:
- Blood Purification, 2018, v. 46, n. 3, p. 239, doi. 10.1159/000488928
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- Publication type:
- Article
Long-Term Therapy With Bevacizumab in a Patient With Glanzmann's Thrombasthenia and Recurrent Digestive Bleeding due to Gastrointestinal Angiodysplastic Lesions.
- Published in:
- American Journal of Gastroenterology (Springer Nature), 2015, v. 110, n. 2, p. 352, doi. 10.1038/ajg.2014.391
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- Publication type:
- Article