Charcot-Marie-Tooth Disease |
AR-CMT2; Charcot-Marie-Tooth disease, type 1; Charcot-Marie-Tooth disease, type 2; Charcot-Marie-Tooth disease, type 4; Charcot-Marie-Tooth Disorder; congenital hypomyelination; Dejerine-Sottas syndrome; DSN; DSS; hereditary motor and sensory neuropathy; HMSN; Peroneal Muscular Atrophy; PMA; Roussy-Levy Syndrome |
Recent Blog Posts
View Post: Charcot–Marie–Tooth disease type 1A: is ascorbic acid effective ...
9 Nov 2009 by Davide Pareyson, Alessandra Solari
Charcot—Marie—Tooth disease (CMT) is the most common hereditary neuropathy, and the most common type of this disorder, CMT1A, is caused by overexpression of peripheral myelin protein 22 (PMP22). 1 Following publication of the paper by ...
View Blog: The Lancet Neurology - http://www.thelancet.com/journals/laneur
View Post: The natural history of Charcot-Marie-Tooth type 1A in adults: a 5 ...
20 Oct 2009 by Verhamme, C., van Schaik, IN, Koelman,...
Charcot–Marie-Tooth type 1A is the most prevalent hereditary demyelinating polyneuropathy. The aim of this study was to investigate the natural history of the disease in adults during a 5-year follow-up and to compare the changes over ...
View Blog: Brain - Advance Access - http://brain.oxfordjournals.org/
View Post: about charcot marie tooth disease
28 Oct 2009 by Tiny
Charcot-Marie-Tooth disease: Definition from Answers.com More about Charcot Marie Tooth Disease: Demographics Signs and symptoms Diagnosis Treatment Prognosis Resources Charcot Marie Tooth Disease Definition -> ...
View Blog: Health Resources - http://www.health-res.com/
View Post: MISSENSE MUTATIONS IN THE SH3TC2 PROTEIN CAUSING CHARCOT-MARIE ...
10 Sep 2009 by Lupo, V., Galindo, MI, Martinez-Rubio,...
Mutations in SH3TC2 (KIAA1985) cause Charcot-Marie-Tooth disease (CMT) type 4C, a demyelinating inherited neuropathy characterized by early onset and scoliosis. Here we demonstrate that the SH3TC2 protein is present in several ...
View Blog: Human Molecular Genetics - Advance Access - http://hmg.oxfordjournals.org/
View Post: Charcot Marie Tooth Disease
19 Oct 2009 by admin
Charcot Marie Tooth Disease or CMT is a is also known also as Hereditary Motor and Sensory Neuropathy (HMSN), Hereditary Sensorimotor Neuropathy (HSMN), or Peroneal Muscular Atrophy. It is a group of heterogeneous inherited disorder of ...
View Blog: Vanillacokefans - http://www.vanillacokefans.com/
View Post: genome.gov
Learning About Charcot-Marie-Tooth Disease
18 Jun 2004 ...
View Blog: http://www.genome.gov/10001204
View Post: First RCT of ascorbic acid for adult Charcot-Marie-Tooth disease ...
9 Oct 2009
Charcot-Marie-Tooth disease type 1A (CMT1A) is a hereditary degenerative peripheral neuropathy that affects roughly 1 in 5000 births. There is currently no specific treatment for this disorder, which is characterised by distal ...
View Blog: NeLM - News - http://www.nelm.nhs.uk/en/NeLM-Area/News/
View Post: Contributions
5 Nov 2009 by Changeling
We do that when we simply say hello to our neighbor, when we serve on a volunteer cleanup committee for a local park, and share our lives with others who have Charcot Marie Tooth disease. In this way, we too have beautified and ...
View Blog: CMTHighlights - http://cmthighlights.blogspot.com/

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