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 9 (September)

1. Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy.
   Ann Neurol, 58(3): 400-10. [Abstract] [Full-text]
2. Ubiquinol: a potential biomarker for tissue energy requirements and oxidative stress.
   Clin Chim Acta, 360(1): 87-96. [Abstract] [Full-text]
3. Sarcoplasmic body myopathy--a rare hereditary myopathy with characteristic inclusions.
   Acta Neurol Scand, 112(4): 223-7. [Abstract] [Full-text]
4. Sleep-related breathing disorder in Duchenne muscular dystrophy: disease spectrum in the paediatric population.
   J Paediatr Child Health, 41(9): 500-3. [Abstract] [Full-text]
5. Targeting the respiratory muscles of fetal sheep for prenatal gene therapy for Duchenne muscular dystrophy.
   Am J Obstet Gynecol, 193(3): 1105-9. [Abstract] [Full-text]
6. Mdm muscular dystrophy: interactions with calpain 3 and a novel functional role for titin's N2A domain.
   Hum Mol Genet, 14(19): 2801-11. [Abstract] [Full-text]
7. Experienced fatigue in facioscapulohumeral dystrophy, myotonic dystrophy, and HMSN-I.
   J Neurol Neurosurg Psychiatry, 76(10): 1406-9. [Abstract] [Full-text]
8. Fatigue and daytime sleepiness rating scales in myotonic dystrophy: a study of reliability.
   J Neurol Neurosurg Psychiatry, 76(10): 1403-5. [Abstract] [Full-text]
9. A neonatal form of Steinert's myotonic dystrophy in twins after in vitro fertilization.
   Fertil Steril, 84(3): 756. [Abstract] [Full-text]
10. Analysis of an adult Duchenne muscular dystrophy population.
    QJM, 98(10): 729-36. [Abstract] [Full-text]
11. Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy.
    Ann Neurol, 58(4): 569-76. [Abstract] [Full-text]
12. Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1.
    Neurol Sci, 26(4): 235-42. [Abstract] [Full-text]

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