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 6 (June)

1. Tachykinergic neurotransmission is enhanced in duodenum from dystrophic (mdx) mice.
   Br J Pharmacol, 145(3): 334-41. [Abstract] [Full-text]
2. Doxycycline attenuates and delays toxicity of the oculopharyngeal muscular dystrophy mutation in transgenic mice.
   Nat Med, 11(6): 672-7. [Abstract] [Full-text]
3. Nutritional inadequacy in adults with muscular dystrophy.
   Muscle Nerve, 31(6): 713-8. [Abstract] [Full-text]
4. Familial clustering of muscular and cardiac involvement in myotonic dystrophy type 1.
   Muscle Nerve, 31(6): 719-24. [Abstract] [Full-text]
5. Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2.
   Muscle Nerve, 31(6): 764-7. [Abstract] [Full-text]
6. Intrapulmonary percussive ventilation vs incentive spirometry for children with neuromuscular disease.
   Arch Pediatr Adolesc Med, 159(6): 526-31. [Abstract] [Full-text]
7. Parents' perspectives on coping with Duchenne muscular dystrophy.
   Child Care Health Dev, 31(4): 385-96. [Abstract] [Full-text]
8. Diffuse xanthogranulomatous pyelonephritis in a patient with myotonic dystrophy and cerebral palsy.
   Int J Urol, 12(5): 497-9. [Abstract] [Full-text]
9. Lipid imaging by gold cluster time-of-flight secondary ion mass spectrometry: application to Duchenne muscular dystrophy.
   J Lipid Res, 46(7): 1388-95. [Abstract] [Full-text]
10. DNA sequence analysis for structure/function and mutation studies in Becker muscular dystrophy.
    Clin Genet, 68(1): 69-79. [Abstract] [Full-text]
11. Relaxin restores altered ileal spontaneous contractions in dystrophic (mdx) mice.
    Ann N Y Acad Sci, 1041: 308-10. [Abstract] [Full-text]
12. Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy.
    J Neurol Neurosurg Psychiatry, 76(7): 1019-21. [Abstract] [Full-text]
13. Localisation of merosin-positive congenital muscular dystrophy to chromosome 4p16.3.
    Hum Genet, 117(2): 207-12. [Abstract] [Full-text]
14. Anatomy of a founder effect: myotonic dystrophy in Northeastern Quebec.
    Hum Genet, 117(2): 177-87. [Abstract] [Full-text]
15. X-linked Emery-Dreifuss muscular dystrophy and vacuoles: an immunohistochemical characterization.
    Muscle Nerve, 32(1): 61-5. [Abstract] [Full-text]
16. Quantitative analysis of the "warm-up" phenomenon in myotonic dystrophy type 1.
    Muscle Nerve, 32(1): 35-42. [Abstract] [Full-text]
17. Functional sparing of intrafusal muscle fibers in muscular dystrophies.
    Muscle Nerve, 32(1): 88-94. [Abstract] [Full-text]
18. Clinical and molecular aspects of the myotonic dystrophies: a review.
    Muscle Nerve, 32(1): 1-18. [Abstract] [Full-text]
19. Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy.
    J Cell Sci, 118: 2923-33. [Abstract] [Full-text]
20. A G-to-A transition at the fifth position of intron-32 of the dystrophin gene inactivates a splice-donor site both in vivo and in vitro.
    Mol Genet Metab, 85(3): 213-9. [Abstract] [Full-text]
21. Generation of skeletal muscle from transplanted embryonic stem cells in dystrophic mice.
    Biochem Biophys Res Commun, 333(2): 644-9. [Abstract] [Full-text]
22. Echocardiographic assessment of left ventricular morphology and function in patients with Emery-Dreifuss muscular dystrophy.
    Int J Cardiol, 102(2): 207-10. [Abstract] [Full-text]
23. Living with a hereditary disease: persons with muscular dystrophy and their next of kin.
    Am J Med Genet A, 136(1): 17-24. [Abstract] [Full-text]

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