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General anesthesia provides similar pain control to nerve block-assisted anesthesia after limb lengthening surgery, common in achondroplasia.
Healthcare professionals generally agree that genetic testing can be useful in the HAE diagnostic process, but many urge caution in interpreting results.
A new study conducted in India has revealed that 40% of antenatal patients experienced severe fetomaternal hemorrhage, which can increase the risk of HDFN.
Researchers have established clinical indications for pediatric blood transfusions with various ABO/Rh blood types that emphasize Rh compatibility.
The prevalence of pregnant women administered anti-D prophylaxis antenatally remains worryingly low in India.
Large language models may offer complementary value to human expert analysis in the diagnosis of achondroplasia and other skeletal dysplasias.
Elevated basal serum tryptase levels in SM and HαT, as well as overlapping clinical characteristics, complicate the diagnostic process for both disorders.
Seladelpar showed efficacy in reducing pruritus and levels of ALP and bilirubin in patients with PBC across multiple clinical trials.
Compound 23, a dual-target FGFR2/3 inhibitor, delivered superior growth improvements over infigratinib in achondroplasia mouse models.
Biomarkers are increasingly recognized for their use in diagnosing and tracking disability progression in NMOSD.
Long-term prophylaxis with lanadelumab has been linked to a marked reduction in attack rates in HAE, with the decline persisting in a real-world setting.
Frailty reduced the likelihood of CLL/SLL first-line treatment initiation during the CIT era, but the gap narrowed with novel therapies.
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