Cure CMD announces CMD BioBank

July 23 2010

To find treatments for the CMDs and identify new CMD genes requires support from the CMD community. If you have CMD or are a sibling or parent of someone with CMD, we would like you to consider supporting CMD Discovery through donating a blood or skin biopsy sample to the CMD BioBank located at the NIGMD respository at the Coriell Medical Institute.
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Congenital Muscular Dystrophy

A group of diseases causing muscle weakness at birth. Several defined genetic mutations cause muscles to break down faster than they can repair or grow. A child with CMD may have various neurological or physical impairments. Some children never gain the ability to walk, while others lose the ability as they grow older. Learn more...
Events
- CMD Research and Therapeutic Development Working Group
  - 13 September 2010
- CMD Translational Grant Deadline
  - 15 September 2010
- Conference on Clinical Research for Rare Diseases
  - 21 September 2010
  - Bethesda, MD
- Cure CMD and NINDS: Common Data Elements Project meeting
  - 29 September 2010
- Team Cure CMD walks/runs San Jose Rock N Roll 1/2 Marathon
  - 3 October 2010
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This website is for the discussion of Congenital muscular dystrophy (CMD) research, treatment and care issues. Please note that the ideas posted are the views of the individual, who may or may not be a licensed professional. Please consult with your doctors before implementing any treatment suggested here.

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Cure CMD announces CMD BioBank

July 23 2010

Congenital Muscular Dystrophy

Events

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