Skip to main content

Home/ Cerebral Palsy/ Group items tagged muscle atrophy

Rss Feed Group items tagged

Filter: All | Bookmarks | Topics Simple Middle
Lee Vander Loop

Muscle Atrophy: MedlinePlus Medical Encyclopedia - 0 views

www.nlm.nih.gov/...003188.htm

muscle atrophy disuse atrophy muscle atrophy and physical therapy physical therapy atrophy

shared by Lee Vander Loop on 23 Jul 10 - Cached
  • Lee Vander Loop on 23 Jul 10
     
    Muscle Atrophy Definition - Types - Causes - Treatment
Lee Vander Loop

Charcot-Marie-Tooth Association - CMTA - 0 views

www.charcot-marie-tooth.org

Charcot-Marie-Tooth Association: tooth CMT international neurology genetics orthopedic peroneal muscular atrophy motor sensory neuropathy degeneration of peroneal muscles muscle functions CMTA CMT expertsorthopedic surgery PMA HMSN

shared by Lee Vander Loop on 29 Mar 10 - Cached
  • Lee Vander Loop on 29 Mar 10
     
    Charcot-Marie-Tooth, or CMT, is the most commonly inherited neurological disorder and is found world-wide in all races and ethnic groups. Discovered in 1886 by three physicians, Jean-Martin-Charcot, Pierre Marie, and Howard Henry Tooth, CMT affects an estimated 2.6 million people. The CMTA is a 501(C)(3)nonprofit organization founded in 1983 whose goals are patient support, public education, promotion of research and ultimately the treatment and cure of CMT. This international group of men and women are noted CMT experts in neurology, genetics, orthopedic surgery, physiatry, physical therapy and podiatry.
Lee Vander Loop

Floppy infant syndrome. [J Clin Neuromuscul Dis. 2004] - PubMed result - 0 views

www.ncbi.nlm.nih.gov/...19078754

floppy infant syndrome floppy infant sydrome at PubMed neurologic disorders ataxic cerebral palsy ataxic hypotonia neurological disorders

shared by Lee Vander Loop on 01 Aug 10 - Cached
  • Lee Vander Loop on 01 Aug 10
     
    National Library of Medicine - National Institute of Health - PubMed Article Abstract: Floppy infant syndrome - Review - On long-term follow up, cerebral palsy and mental retardation turn out to be the 2 most common causes of FIS. This review focuses on neuromuscular causes of FIS. With the advent of molecular diagnosis, a few conditions can be diagnosed by DNA analysis of the peripheral lymphocytes (myotonic dystrophy, spinal muscular atrophy); however, for the most part, electrodiagnostic studies and muscle biopsy remain as essential diagnostic tools for FIS.
1 - 3 of 3
Showing 20▼ items per page