About PWSPrader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder caused by an abnormality in the gene expression on chromosome 15. The Prader-Willi Syndrome Association USA ...

Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder caused by an abnormality in the gene expression on chromosome 15. The Prader-Willi Syndrome Association USA estimates that PWS ...

Four years before Kimberly Gallagher enrolled in Medicaid herself, the public health insurance program's rules prompted her ...

G. Willi-Food International (NASDAQ:WILC) has had a great run on the share market with its stock up by a significant 24% over the last three months. But the company's key financial indicators ...

Willi Carlisle brands himself a believer in nonsense on 'Winged Victory,' pairing original, fantastical tracks with contemporary translations of boundary-pushing, subversive relics.

On Winged Victory, songwriter Willi Carlisle weaves between the absurd and the sentimental. NPR's Scott Simon speaks with Carlisle about the 11 tracks of originals and covers.

The first words that Arkansas-forged singer-songwriter Willi Carlisle sings on his magnificent fourth album, “Winged Victory,” are not his own. Atop a flurry of bluegrass banjo and harmonica ...

A rare genetic condition called Prader-Willi syndrome, in addition to autism, left him with an intellectual disability; a constant, excessive hunger; and an inability to speak.

An unexpected logo change at China’s securities regulator is being teasingly celebrated by stock investors as heralding an end to recent years of market malaise.

The next Architecture set that was just announced is the Bavarian castle Neuschwanstein, one of the inspirations for Sleeping Beauty's castle at Disneyland (and on the logo).

The latest G.Willi-Food International LtdShs stock prices, stock quotes, news, and WILC history to help you invest and trade smarter.

Colin Farrell opened up to PEOPLE about his son James, who was diagnosed with Angelman syndrome. Here’s what to know about the rare neurogenetic disorder that affects 1 in 15,000 people.