Spinal muscular atrophy: Difference between revisions
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===[[Spinal Muscular atrophy carrier testing and newborn screening | Carrier testing and newborn screening]]=== | ===[[Spinal Muscular atrophy carrier testing and newborn screening | Carrier testing and newborn screening]]=== | ||
===[[Spinal Muscular atrophy epidemiology| Epidemiology]]=== | ===[[Spinal Muscular atrophy epidemiology and demographics| Epidemiology and Demographics]]=== | ||
===[[Spinal Muscular atrophy other forms | Other forms]]=== | ===[[Spinal Muscular atrophy other forms | Other forms]]=== | ||
Revision as of 20:30, 24 June 2011
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Spinal Muscular Atrophy Microchapters |
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Spinal muscular atrophy Resources |
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Ongoing Trials on Spinal muscular atrophy at Clinical Trials.gov |
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US National Guidelines Clearinghouse on Spinal muscular atrophy |
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Risk calculators and risk factors for Spinal muscular atrophy |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [2] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
Overview
Symptom
Types
Causes
Diagnosis
Carrier testing and newborn screening
Epidemiology and Demographics
Other forms
Treatment
Outcome measures in SMA|Therapeutics development in SMA
Research
References
External links
- Template:NINDS
- SMA Support
- Spinal Muscular Atrophy - Fight SMA - An international nonprofit dedicated to finding a treatment or cure for spinal muscular atrophy. Visit Fight SMA's website and also the Spinal Muscular Atrophy Blog for the latest news and research information about the leading genetic killer of children under two.
- Families of Spinal Muscular Atrophy - An international nonprofit dedicated to advancing research and supporting individuals and families with sma. FSMA has a web site with news, information and message boards for individuals to post questions. FSMA is one of the largest US private funders of SMA research and has more than 30 chapters worldwide.FSMA
- SMA Trust - a UK registered charity working to fund medical research into Spinal Muscular Atrophy
- Jennifer Trust for Spinal Muscular Atrophy - A national charity in the UK dedicated both to supporting people affected by SMA, and investing in essential research into causes, treatments and eventually a cure for the condition
Template:Diseases of the nervous system Template:SIB
da:Spinal muskulær atrofi de:Spinale Muskelatrophie el:Νωτιαία μυϊκή ατροφία nl:Spinale Musculaire Atrofieën fi:Spinaaliset lihasatrofiat sv:Spinal muskelatrofi