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Research Feature
It’s been called the most common disease nobody’s heard of – and also one of the big mysteries in medicine. It’s restless legs syndrome (RLS) , a neurological and sleep disorder that causes discomfort and sometimes pain in the legs, particularly at night. It triggers a constant urge to move the legs that makes falling asleep and staying asleep...
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Research Features
Chris Camp recalls the early days of the HIV/AIDS epidemic, when being diagnosed as HIV positive was considered a virtual death sentence. Doctors had no medications that could really help. People with the disease often did not survive more than a year or two. Camp, now 63, says he personally lost more than 500 friends. Among them: his first husband...
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Research Feature
Soon after birth, a baby in the United States is tested for sickle cell disease, the often-devastating genetic blood disorder affecting more than 100,000 Americans and 20 million of people worldwide. If positive, that newborn typically begins a course of treatment that can greatly prolong life and help stave off complications of the disease. But in...
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Transfusion journal
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Research Feature
Every two seconds someone in the United States needs blood. Five million people receive a blood transfusion every year in the U.S. In a country where blood is perennially in short supply, it is the most common medical procedure of all. Yet giving to a blood bank is not always a slam dunk—some people get turned away because of strict rules meant for...
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News Release
Los Institutos Nacionales de la Salud (NIH, por sus siglas en inglés) anunciaron hoy el lanzamiento de una iniciativa para acelerar la búsqueda de curas para la enfermedad de células falciformes, un grupo de trastornos sanguíneos hereditarios que afectan al menos a 100,000 personas de Estados Unidos y 20 millones en todo el mundo. A partir de los...
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Research Feature
They ranged in age from 15 to 61—four African American women, all with stories to tell about their struggles with sickle cell disease, all with stories about a common experience that helped them through those struggles: participating in clinical trials. It mattered, said the women, all of whom had joined trials funded by the National Institutes of...
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News Release
Scientists have confirmed the role of a set of gene mutations in the development of congenital heart disease and simultaneously discovered a link between them and some neurodevelopmental abnormalities in children. These abnormalities include cognitive, motor, social, and language impairments. “The risk of developing neurodevelopmental disabilities...