Muscular Dystrophy Research - Duchenne Muscular Dystrophy, Symptoms, Treatment

Muscular Dystrophy Research Today is a free monthly online journal that collates and summarizes the latest research about Muscular Dystrophy, including details on duchenne muscular dystrophy, symptoms, treatment.


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Volume 3 (2007), Issue 1 (January)

  1. Endurance training: an effective and safe treatment for patients with LGMD2I.
    Neurology, 68(1): 59-61. [Abstract] [Full-text]
  2. Nitric oxide release combined with nonsteroidal antiinflammatory activity prevents muscular dystrophy pathology and enhances stem cell therapy.
    Proc Natl Acad Sci U S A, 104(1): 264-9. [Abstract] [Full-text]
  3. Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutations.
    J Med Genet, 44(1): 38-43. [Abstract] [Full-text]
  4. MRI for the demonstration of subclinical muscle involvement in muscular dystrophy.
    Clin Radiol, 62(2): 160-5. [Abstract] [Full-text]
  5. Orofacial dysfunction in children and adolescents with myotonic dystrophy.
    Dev Med Child Neurol, 49(1): 18-22. [Abstract] [Full-text]
  6. Kinetics of FcRn-mediated recycling of IgG and albumin in human: pathophysiology and therapeutic implications using a simplified mechanism-based model.
    Clin Immunol, 122(2): 146-55. [Abstract] [Full-text]
  7. A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12.
    Brain, 130: 368-80. [Abstract] [Full-text]
  8. Deletion of exon 16 of the dystrophin gene is not associated with disease.
    Hum Mutat, 28(2): 205. [Abstract] [Full-text]
  9. Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy.
    Hum Mutat, 28(2): 196-202. [Abstract] [Full-text]
  10. Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene.
    Hum Mutat, 28(2): 183-95. [Abstract] [Full-text]
  11. Belated diagnosis of congenital myotonic dystrophy in a boy with cerebral palsy.
    Am J Phys Med Rehabil, 86(2): 161-5. [Abstract] [Full-text]
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Muscular Dystrophy Research Today Archive:

Volume 1 (2005)
  Issue 1 (January)
  Issue 2 (February)
  Issue 3 (March)
  Issue 4 (April)
  Issue 5 (May)
  Issue 6 (June)
  Issue 7 (July)
  Issue 8 (August)
  Issue 9 (September)
  Issue 10 (October)
  Issue 11 (November)
  Issue 12 (December)

Volume 2 (2006)
  Issue 1 (January)
  Issue 2 (February)
  Issue 3 (March)
  Issue 4 (April)
  Issue 5 (May)
  Issue 6 (June)
  Issue 7 (July)
  Issue 8 (August)
  Issue 9 (September)
  Issue 10 (October)
  Issue 11 (November)
  Issue 12 (December)

Volume 3 (2007)
  Issue 1 (January)
  Issue 2 (February)
  Issue 3 (March)
  Issue 4 (April)
  Issue 5 (May)
  Issue 6 (June)
  Issue 7 (July)
  Issue 8 (August)
  Issue 9 (September)
  Issue 10 (October)
  Issue 11 (November)
  Issue 12 (December)

Volume 4 (2008)
  Issue 1 (January)
  Issue 2 (February)
  Issue 3 (March)
  Issue 4 (April)
  Issue 5 (May)
  Issue 6 (June)
  Issue 7 (July)
  Issue 8 (August)
  Issue 9 (September)
  Issue 10 (October)



Muscular Dystrophy Books

Chance of a Lifetime (Silver Blades)

Chance of a Lifetime (Silver Blades)