Wilson's Disease is a rare inherited disorder in which copper accumulates in the body to harmful levels. Although copper supports essential functions such as enzyme activity, brain development and ...

This multimodal MRI study shows that hepatic iron deposition, brain iron accumulation, and selective brain atrophy differ ...

Achieving a diagnosis of WD is dependent on maintaining a high index of suspicion. On the basis of a recent case report, [25] it is recommended that all subjects presenting with symptomatic or ...

Oppenheimer has initiated Monopar Therapeutics at outperform citing the potential of a candidate for the genetic disorder Wilson disease it acquired from AstraZeneca (AZN). The firm set a $77 price ...

Dear Dr. Roach: Our son passed away at 38 years old this past December with an end-stage alcohol-related liver disease. He had been sober for four years prior to this, but blood tests revealed that he ...

In another example of the effect of modifier genes, Schiefermeier et al [45] tried to delineate why some patients have later-onset neurologic as well as hepatic symptoms by examining the potential ...

Wilson’s disease is not something most people would think about, until it suddenly enters a conversation, often through a story that feels too close to home. It is a rare genetic condition, quiet in ...

-- Initial positive data from Phase 1/2 clinical trial of PM359 in CGD provide clinical proof-of-concept for Prime Editing as a transformative gene editing technology -- -- On-track to file IND and/or ...