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 12 (December)

1. Simultaneous mutation scanning for gross deletions, duplications and point mutations in the DMD gene.
   Eur J Hum Genet, 16(1): 53-61. [Abstract] [Full-text]
2. Multiple mitochondrial DNA deletions in monozygotic twins with OPMD.
   J Neurol Neurosurg Psychiatry, 79(1): 68-71. [Abstract] [Full-text]
3. Facioscapulohumeral muscular dystrophy: a multicenter study on hearing function.
   Audiol Neurootol, 13(1): 1-6. [Abstract] [Full-text]
4. Acute liver failure following therapeutic paracetamol administration in patients with muscular dystrophies.
   Anaesthesia, 63(1): 89-91. [Abstract] [Full-text]
5. Three-point technique of fat quantification of muscle tissue as a marker of disease progression in Duchenne muscular dystrophy: preliminary study.
   AJR Am J Roentgenol, 190(1): W8-12. [Abstract] [Full-text]
6. Local dystrophin restoration with antisense oligonucleotide PRO051.
   N Engl J Med, 357(26): 2677-86. [Abstract] [Full-text]
7. Array-MLPA: comprehensive detection of deletions and duplications and its application to DMD patients.
   Hum Mutat, 29(1): 190-7. [Abstract] [Full-text]
8. RNA toxicity in myotonic muscular dystrophy induces NKX2-5 expression.
   Nat Genet, 40(1): 61-8. [Abstract] [Full-text]

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