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.

Volume 1 (2005), Issue 5 (May)

1. Merosin-negative congenital muscular dystrophy: magnetic resonance spectroscopy findings.
   Brain Dev, 27(4): 308-10. [Abstract] [Full-text]
2. Brain magnetic resonance image changes in a family with congenital and classic myotonic dystrophy.
   Brain Dev, 27(4): 291-6. [Abstract] [Full-text]
3. Aerobic training in patients with myotonic dystrophy type 1.
   Ann Neurol, 57(5): 754-7. [Abstract] [Full-text]
4. Congenital muscular dystrophy: molecular and cellular aspects.
   Cell Mol Life Sci, 62(7): 809-23. [Abstract] [Full-text]
5. A family of Emery-Dreifuss muscular dystrophy with extreme difference in severity.
   Pediatr Neurol, 32(5): 358-60. [Abstract] [Full-text]
6. LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype.
   Neurology, 64(9): 1635-7. [Abstract] [Full-text]
7. A comparison of gait in spinal muscular atrophy, type II and Duchenne muscular dystrophy.
   Gait Posture, 21(4): 369-78. [Abstract] [Full-text]
8. Merosin-deficient congenital muscular dystrophy (CMD): a study of 25 Brazilian patients using MRI.
   Pediatr Radiol, 35(6): 572-9. [Abstract] [Full-text]
9. Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs.
   J Neurol, 252(5): 538-47. [Abstract] [Full-text]
10. Significance of Beevor's sign in facioscapulohumeral dystrophy and other neuromuscular diseases.
    J Neurol Neurosurg Psychiatry, 76(6): 869-70. [Abstract] [Full-text]
11. Transgenic mice expressing CUG-BP1 reproduce splicing mis-regulation observed in myotonic dystrophy.
    Hum Mol Genet, 14(11): 1539-47. [Abstract] [Full-text]
12. Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA).
    Hum Genet, 117(1): 92-8. [Abstract] [Full-text]
13. A 1.3 kb promoter fragment confers spatial and temporal expression of utrophin A mRNA in mouse skeletal muscle fibers.
    Neuromuscul Disord, 15(6): 437-49. [Abstract] [Full-text]
14. Effects of fukutin deficiency in the developing mouse brain.
    Neuromuscul Disord, 15(6): 416-26. [Abstract] [Full-text]
15. Subclinical cardiac involvement in patients with facioscapulohumeral muscular dystrophy.
    Neuromuscul Disord, 15(6): 403-8. [Abstract] [Full-text]
16. Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display.
    Eur J Hum Genet, 13(6): 721-30. [Abstract] [Full-text]
17. Rapid progression from hypertrophic cardiomyopathy to heart failure in a patient with Becker's muscular dystrophy.
    Eur J Heart Fail, 7(4): 684-8. [Abstract] [Full-text]

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