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 3 (2007), Issue 9 (September)

1. Reduced cell anchorage may cause sarcolemma-specific collagen VI deficiency in Ullrich disease.
   Neurology, 69(10): 1043-9. [Abstract] [Full-text]
2. Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan.
   Neurology, 69(10): 1035-42. [Abstract] [Full-text]
3. Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD.
   Neurology, 69(10): 1018-26. [Abstract] [Full-text]
4. Molecular heterogeneity in fetal forms of type II lissencephaly.
   Hum Mutat, 28(10): 1020-7. [Abstract] [Full-text]
5. Tranexamic acid diminishes intraoperative blood loss and transfusion in spinal fusions for duchenne muscular dystrophy scoliosis.
   Spine, 32(20): 2278-83. [Abstract] [Full-text]
6. Family function in families of children with Duchenne muscular dystrophy.
   Fam Community Health, 30(4): 296-304. [Abstract] [Full-text]
7. New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation.
   Neurology, 69(12): 1254-60. [Abstract] [Full-text]
8. Charcot-Marie-Tooth neuropathy type 1A combined with Duchenne muscular dystrophy.
   Eur J Neurol, 14(10): 1182-5. [Abstract] [Full-text]
9. Antisense-mediated exon skipping: a versatile tool with therapeutic and research applications.
   RNA, 13(10): 1609-24. [Abstract] [Full-text]

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