Results 281 to 290 of about 1,468,461 (396)
ABSTRACT Introduction Decision‐making in haemophilia is challenging due to the small evidence base, disease heterogeneity, and inter‐patient variability. Shared decision‐making (SDM) supports patient‐clinician decisions. Aim Creation of a two‐sided decision box facilitating SDM for haemophilia patients switching from conventional (weight‐based) to ...
Arun Keepanasseril+4 more
wiley +1 more source
Estimating the Factor VIII‐Equivalent Activity of Emicizumab Using Global Assays of Haemostasis
ABSTRACT Background Emicizumab is a bispecific monoclonal antibody mimicking factor (F) VIII activity and an effective therapy for prophylaxis in people with haemophilia A (PWHA). The FVIII‐equivalent activity (FVIIIeq) of emicizumab remains unknown. Objectives To estimate FVIIIeq of emicizumab using global assays of haemostasis.
Daniel Kraemmer+6 more
wiley +1 more source
Platforms for studying cell–cell recognition by immune cells
This review compares different platforms for studying how immune cells integrate signals from co‐signaling receptor‐ligand interactions at cell–cell interfaces. By understanding the strengths and weaknesses of each platform, including which factors can be controlled by the user, immunologists can identify the most appropriate platform to address their ...
Jordan Kramer+2 more
wiley +1 more source
Abstract The survival of newly diagnosed patients with multiple myeloma has improved significantly over the past 20 years with significant therapeutic advances. Despite this, high‐dose chemotherapy followed by autologous stem cell transplantation remains the standard of care in newly diagnosed patients who are considered transplant eligible.
Georgia McCaughan+14 more
wiley +1 more source
Abstract Background Apheresis procedure of autologous lymphocytes competent for proliferation and expansion is a crucial step in the production of chimeric antigen receptor (CAR) T‐cells. Previous therapies or disease status prior to collection may negatively impact the collections.
Vladan Vučinić+25 more
wiley +1 more source
Abstract The discovery of activating mutations in the epidermal growth factor receptor (EGFR) gene has revolutionized the management of lung cancer, enabling the development of targeted tyrosine kinase inhibitors (TKIs). These therapies offer improved survival and reduced side effects compared with conventional treatments.
Maxime Borgeaud+9 more
wiley +1 more source
Alternative Immunosuppression in Acquired Haemophilia A
Haemophilia, EarlyView.
Jayna Mistry+3 more
wiley +1 more source
What's new? Mutations in EGFR are the most frequently detected driver mutations in non‐small cell lung carcinoma (NSCLC), and two common mutations account for 75%–90% of these. The remaining 10%–25% are uncommon mutations, a heterogeneous set of genetic changes that do not necessarily respond well to treatment.
Yuwen Xie+7 more
wiley +1 more source
TGF‐β inhibition is emerging as a promising cancer therapy, yet translating laboratory success to bedside implementation has suffered significant setbacks. The associated challenges include adverse drug reactions, inadequate predictive models, and activation of alternative signaling pathways.
Faizah A. Alabi+5 more
wiley +1 more source