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Decoding Patient's Genome Found Gene For Inherited Neurological Disorder CMT
Heralding what they hope is a new era of personalized genomic medicine, experts in the US have identified the gene behind a patient's inherited neurological disorder, in this case a form of Charcot-Marie-Tooth disease, by sequencing his complete genome.

Medical News Today: Mar 11 2010 1:51PM
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Reminder Webcast Alert: Transgenomic, Inc. Announces Fourth Quarter 2009 Earnings Release Conference Call Webc
KSLA Heart News OMAHA, Neb., Feb.

24 /PRNewswire-FirstCall/ -- Transgenomic, Inc.

(OTC Bulletin Board: TBIO) announces the following Webcast: What: Transgenomic, Inc.

Fourth Quarter 2009 Earnings Release Conference Call When: Wednesday, February 24, 2010 ...

KSLA: Feb 25 2010 3:26AM
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Maternal Coagulation Disorders and Postpartum Hemorrhage
Silver RM et al.

Disorders of coagulation are relatively uncommon as a sole cause of postpartum hemorrhage.

Coagulation disturbances should be suspected in patients with a family history of such abnormalities and patients with a history of...

MDLinx: Feb 16 2010 11:55AM
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Octapharma Accepting Grant Applications for Research on Immunotherapy, Coagulation Disorders, and Critical Car
Octapharma USA is accepting applications until the end of March 2010 for the Octapharma 25th Anniversary Grants Program, which supports clinical or pre-clinical research focused on human protein therapies in coagulation disorders, immunotherapy, intensive care,...

The Foundation Center: Feb 16 2010 5:23AM
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