Biomarkers are increasingly recognized for their use in diagnosing and tracking disability progression in NMOSD.

The duration of P-waves and the PQ interval is shortened in adult patients with Fabry disease before the onset of cardiomyopathy, a study found.

The pathophysiology of Duchenne muscular dystrophy (DMD) revolves around the lack of functional dystrophin, which results in a fragile, permeable cell membrane and the dysregulation of calcium ...

Diet and nutrition play a key role in managing Duchenne muscular dystrophy (DMD). Dietary goals include preserving lean muscle mass, preventing weight gain and fat accumulation, maintaining bone ...

Spesolimab demonstrated rapid and effective disease control in a patient with generalized pustular psoriasis (GPP) undergoing hemodialysis.

Monomeric C-reactive protein (mCRP) levels were significantly elevated in AAV and declined earlier than pentameric CRP during treatment.

An extension of the dosing interval of lanadelumab retains effectiveness in reducing attack frequency in patients with HAE.

US Food and Drug Administration grants Orphan Drug Designation to VAS-101 for patients with sickle cell disease (SCD).

As someone living with neuromyelitis optica (NMO), my initial reaction to the words, “stem cell transplant,” is to run in the opposite direction.

In those with HAE-C1NH, whole blood under cold activation demonstrated a noticeable elevation in bradykinin levels, with minimal impact on healthy subjects.

Patients with antiaquaporin 4 antibody-positive NMOSD and MOGAD often also have other comorbidities, a study found.

Bisphosphonate scintigraphy has a high diagnostic accuracy in ATTR-CM caused by a Glu54Gln mutation in the TTR gene.