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 7 (July)

1. Molecular cloning and protein expression of Duchenne muscular dystrophy gene products in porcine retina.
   Neuromuscul Disord, 15(7): 476-87. [Abstract] [Full-text]
2. Recurrent somatic mosaicism for D4Z4 contractions in a family with facioscapulohumeral muscular dystrophy.
   Neuromuscul Disord, 15(7): 471-5. [Abstract] [Full-text]
3. CINRG randomized controlled trial of creatine and glutamine in Duchenne muscular dystrophy.
   Ann Neurol, 58(1): 151-5. [Abstract] [Full-text]
4. Midwall myocardial fibrosis in Becker-Kiener muscular dystrophy.
   Z Kardiol, 94(7): 465-8. [Abstract] [Full-text]
5. Stable transduction of myogenic cells with lentiviral vectors expressing a minidystrophin.
   Gene Ther, 12(14): 1099-108. [Abstract] [Full-text]
6. Altered mRNA splicing of the skeletal muscle ryanodine receptor and sarcoplasmic/endoplasmic reticulum Ca2+-ATPase in myotonic dystrophy type 1.
   Hum Mol Genet, 14(15): 2189-200. [Abstract] [Full-text]
7. Expression and regulation of CC class chemokines in the dystrophic (mdx) diaphragm.
   Am J Respir Cell Mol Biol, 33(2): 178-85. [Abstract] [Full-text]
8. HnRNP H inhibits nuclear export of mRNA containing expanded CUG repeats and a distal branch point sequence.
   Nucleic Acids Res, 33(12): 3866-74. [Abstract] [Full-text]
9. Oxidative stress in myotonic dystrophy type 1.
   Free Radic Res, 39(7): 771-6. [Abstract] [Full-text]
10. Hutterite brothers both affected with two forms of limb girdle muscular dystrophy: LGMD2H and LGMD2I.
    Eur J Hum Genet, 13(8): 978-82. [Abstract] [Full-text]
11. Tracheoinnominate fistula in a Duchenne muscular dystrophy patient: successful management with an endovascular stent.
    Neuromuscul Disord, 15(8): 569-71. [Abstract] [Full-text]
12. Impaired primary hemostasis with normal platelet function in Duchenne muscular dystrophy during highly-invasive spinal surgery.
    Neuromuscul Disord, 15(8): 532-40. [Abstract] [Full-text]
13. Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genes.
    Neuromuscul Disord, 15(8): 521-4. [Abstract] [Full-text]

© 2005-2008 Muscular Dystrophy Research Today. All Rights Reserved.