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Storage Disease
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Storage Disease
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Should I be tested for Tay-Sachs disease? Nov 22, 2005
TSD is considered a lysosomal (a small component of the cell) storage disease in which substances called gangliosides accumulate throughout the body, causing ...
- Standard-Speaker,
Child with rare illness fights for life Nov 13, 2005
Joshua Sorenson, 5, was born with glycogen storage disease type 1, a condition which requires strict diet regulation, special feedings and no sugar. ...
- Provo Daily Herald,
Rare Disorder Patients Face Access Restrictions on Expensive ... Nov 9, 2005
For many people with rare illnesses such as lysosomal storage disease, hemophilia, Guillain-Barre syndrome, and Alpha-1-antitrypsin deficiency disease ...
- Genetic Engineering News,
Students, community unite to fund liver for ailing baby Oct 25, 2005
Canon Perkins, a 19-month-old boy from Amarillo, has been diagnosed with the liver disease, Glycogen Storage Disease Type IV, said his father, Drew Perkins. ...
- Texas Tech Daily Net,
flexSCAN Reaches Open Enrollment Milestone; Record 110,000 ... Oct 26, 2005
Disease screening and benchmarking services are provided from a mobile clinic that goes on-site to qualifying employer locations. ...
- Business Wire (press release),
One stolen puppy doomed Sep 26, 2005
Massey researchers say Beau is a carrier of mucopolysaccharidosis, also known as storage disease, or MP3a, which is present in humans under the name San ...
- Stuff.co.nz
Short takes on people, places and events Sep 16, 2005
Dr. Paul Fernhoff, the director of the Emory Lysosomal Storage Disease Center, said the disease is most prevalent in the Jewish community. ...
- Atlanta Jewish Times
What rare diseases can teach us Sep 3, 2005
Once again, NP-C is a good example. It is what is known as a "lysosomal storage" disease — one that involves a tiny structure in cells known as the lysosome. ...
- Los Angeles Times
Snatched huntaway pups in good shape after ordeal Aug 30, 2005
Instead they were privately owned and were being treated for the genetic wasting disease, mucopolysaccaridosis, sometimes known as storage disease. ...
- Manawatu Standard
Hepatocyte transplantation for metabolic liver disease: UK ...Jul 29, 2005
...been gained in patients with acute liver failure 3,4 and metabolic liver diseases such as Crigler–Najjar syndrome type I, 5 glycogen storage disease type 1a ...
- Journal of the Royal Society of Medicine
Changed dreamsJul 29, 2005
...month wellness check, the doctor noticed something was wrong with Canon's liver, and after numerous tests, he was diagnosed with glycogen storage disease type 4 ...
- Amarillo.com (Subscription)
Treatments now available for lysosomal storage diseasesJul 1, 2005
...additional LSDs, including Tay-Sachs disease, Neimann-Pick types B and C, Pompe disease, MPS II, MPS VI and Wolman disease/cholesterol ester storage disease. ...
- AAP News (subscription)
Hannah's champJul 23, 2005
The 11-year-old from Osawatomie, Kan., is in dire need of a liver transplant after having lived with the effects of glycogen storage disease since she was 6 ...
- Blue Springs Examiner
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Storage Disease
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