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 2 (2006), Issue 2 (February)

1. Use of RNA fluorescence in situ hybridization in the prenatal molecular diagnosis of myotonic dystrophy type I.
   Clin Chem, 52(2): 319-22. [Abstract] [Full-text]
2. Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2).
   Biochim Biophys Acta, 1762(3): 329-34. [Abstract] [Full-text]
3. Oxandrolone enhances skeletal muscle myosin synthesis and alters global gene expression profile in Duchenne muscular dystrophy.
   Am J Physiol Endocrinol Metab, 290(3): E530-9. [Abstract] [Full-text]
4. Spectrum of brain changes in patients with congenital muscular dystrophy and FKRP gene mutations.
   Arch Neurol, 63(2): 251-7. [Abstract] [Full-text]
5. Falls and stumbles in myotonic dystrophy.
   J Neurol Neurosurg Psychiatry, 77(3): 393-6. [Abstract] [Full-text]
6. Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1.
   Nature, 439(7079): 973-7. [Abstract] [Full-text]
7. Outcome and effect of pregnancy in myotonic dystrophy type 2.
   Neurology, 66(4): 579-80. [Abstract] [Full-text]
8. Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?
   Biochem Biophys Res Commun, 342(2): 489-502. [Abstract] [Full-text]

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