Modern prophylactic therapies for hereditary angioedema with C1 inhibitor deficiency (HAE-C1INH) have become increasingly prevalent in Hungary, paralleling global trends, and are proving both ...

Physical activity before or during pregnancy was not associated with negative maternal/neonatal outcomes; however, physical activity was not statistically significantly associated with positive ...

There were no significant changes in the levels of a polysialic acid (polySia), a glycoepitope that plays a key role during neuronal development and plasticity, in chronic inflammatory demyelinating ...

Complement inhibition appears to effectively block lesion extension as well as facilitate oligodendrocyte repopulation and myelin repair during acute attacks of neuromyelitis optica spectrum disorder ...

A CRISPR/Cas9-modified Janus kinase 2 (JAK2) V617F model may be useful to develop new therapies against myeloproliferative neoplasms (MPNs), showed a new study published in the International Journal ...

Capillary zone electrophoresis appears to effectively identify molecular fragments capable of binding to human transthyretin (TTR), with potential therapeutic applications for transthyretin amyloid ...

Stem cell therapy, artificial womb technology, and telehealth innovations are reshaping neonatal care and improving outcomes for infants affected by complex conditions, including fetal and neonatal ...

The presence of Raynaud’s phenomenon and assessment with nailfold videocapillaroscopy (NVC) may identify patients with systemic lupus erythematosus (SLE) who are at high risk of pulmonary arterial ...

Researchers in the United States have observed an increase in the incidence of systemic mastocytosis (SM), particularly among non-Hispanic white individuals. SM is a rare mast cell disorder ...

Venetoclax (VEN)-based therapies are effective after disease progression while receiving covalent Bruton tyrosine kinase inhibitors (cBTKi) in patients with chronic lymphocytic leukemia (CLL), ...

Patients with severe hemophilia A and B who develop inhibitors exhibit fundamentally distinct immune responses to replacement factor VIII and factor IX, as revealed by single-cell sequencing of ...

Risk factors for thymidine kinase 2 deficiency (TK2d) include inheritance patterns, molecular pathogenesis, genotype-phenotype correlations, and the risk of secondary complications after disease onset ...