Paralysis Research Today is a free monthly online journal that collates and summarizes the latest research about Paralysis, including details on treatment, diagnosis, facial paralysis, sleep paralysis.

Volume 1 (2004), Issue 2 (November)

1. Distal arthrogryposis 5: a dominant syndrome of peripheral contractures and ophthalmoplegia.
   Am J Med Genet A, 131(1): 67-70. [Abstract] [Full-text]
2. Myosin heavy chain isoform mRNA and protein levels after long-term paralysis.
   Biochem Biophys Res Commun, 325(1): 296-301. [Abstract] [Full-text]
3. Striking intrafamilial phenotypic variability and spastic paraplegia in the presence of similar homozygous expansions of the FRDA1 gene.
   Mov Disord, 19(12): 1424-31. [Abstract] [Full-text]
4. Cardiovascular control during voluntary static exercise in humans with tetraplegia.
   J Appl Physiol, 97(6): 2077-82. [Abstract] [Full-text]
5. The role of glottal gap in predicting aspiration in patients with unilateral vocal paralysis.
   Clin Otolaryngol Allied Sci, 29(6): 709-12. [Abstract] [Full-text]
6. A brief exploration of neurological art history.
   J Hist Neurosci, 13(4): 345-50. [Abstract] [Full-text]
7. Pathological substrate for regional distribution of increased atrophy rates in progressive supranuclear palsy.
   J Neurol Neurosurg Psychiatry, 75(12): 1772-5. [Abstract] [Full-text]
8. Paraplegia secondary to fracture-subluxation of the thoracic spine sustained playing rugby union football.
   Br J Sports Med, 38(6): e32. [Abstract] [Full-text]
9. Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the 5698G-->A mitochondrial DNA mutation.
   Neuromuscul Disord, 14(12): 815-7. [Abstract] [Full-text]
10. Application of multiplex ligation-dependent probe analysis to define a small deletion encompassing PMP22 exons 4 and 5 in hereditary neuropathy with liability to pressure palsies.
    Neuromuscul Disord, 14(12): 804-9. [Abstract] [Full-text]
11. A founder effect in three large Newfoundland families with a novel clinically variable spastic ataxia and supranuclear gaze palsy.
    Am J Med Genet A, 131(3): 249-54. [Abstract] [Full-text]

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