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Healthcare professionals generally agree that genetic testing can be useful in the HAE diagnostic process, but many urge caution in interpreting results.
Researchers have established clinical indications for pediatric blood transfusions with various ABO/Rh blood types that emphasize Rh compatibility.
Researchers developed a new clinical score to estimate the probability of NMOSD in patients presenting with optic neuritis.
Patients with alpha-1 antitrypsin deficiency (AATD) and the PiZZ genotype have more aggressive disease than those with PiSZ.
Two phase 3 clinical trials are recruiting patients with CIDP to evaluate the efficacy of riliprubart treatment.
Generalized pustular psoriasis is the most serious form of psoriasis, with more than half of all patients with the condition needing hospitalization.
Rilzabrutinib shows improved platelet counts, reduced fatigue, and acceptable safety for patients with immune thrombocytopenia (ITP).
A 16-year-old boy with Duchenne muscular dystrophy died of acute liver failure several months after receiving delandistrogene moxeparvovec-rokl (Elevidys®).
The CSHA Clinical Frailty Scale is a feasible tool for predicting treatment-related toxicity and discontinuation in older adults with CLL.
A new phase 2 clinical trial to test the safety, efficacy, and tolerability of TAK-411 for the treatment of CIDP is now open.
The EGPA treatment mepolizumab has shown safety and efficacy in decreasing the absolute number of eosinophils in peripheral blood and tissues.
The expression of AQP4 In the respiratory epithelium suggests that lung involvement might be an unrecognized feature of NMOSD. Patients with neuromyelitis optica spectrum disorder (NMOSD) should be ...
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