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 3 (December)

1. Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects.
   J Biol Chem, 279(50): 51844-50. [Abstract] [Full-text]
2. Signal acquisition and analysis for cortical control of neuroprosthetics.
   Curr Opin Neurobiol, 14(6): 758-62. [Abstract] [Full-text]
3. Selecting the signals for a brain-machine interface.
   Curr Opin Neurobiol, 14(6): 720-6. [Abstract] [Full-text]
4. Ophthalmic management of facial nerve palsy.
   Eye, 18(12): 1225-34. [Abstract] [Full-text]
5. Differences in kinematic parameters and plantarflexor reflex responses between manual (Ashworth) and isokinetic mobilisations in spasticity assessment.
   Clin Neurophysiol, 116(1): 93-100. [Abstract] [Full-text]
6. Complete recovery of severe quadriparesis caused by stab wound at the craniocervical junction.
   Neurosurg Rev, 28(1): 70-2. [Abstract] [Full-text]
7. A novel autosomal recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12.
   Brain, 128: 42-51. [Abstract] [Full-text]
8. Dopamine transporter SPECT in patients with mitochondrial disorders.
   J Neurol Neurosurg Psychiatry, 76(1): 118-20. [Abstract] [Full-text]
9. The spasticity paradox: movement disorder or disorder of resting limbs?
   J Neurol Neurosurg Psychiatry, 76(1): 47-54. [Abstract] [Full-text]
10. Enigmatic osteomyelitis and bilateral upper limb palsy in a neonate.
    Pediatr Neurol, 32(1): 56-9. [Abstract] [Full-text]
11. A novel thymidine phosphorylase mutation in a Spanish MNGIE patient.
    J Neurol Sci, 228(1): 35-9. [Abstract] [Full-text]
12. Prolonged hemidiaphragmatic paralysis following interscalene brachial plexus block.
    J Clin Anesth, 16(8): 573-5. [Abstract] [Full-text]
13. Mutation analysis of the KIF21A gene in an Indian family with CFEOM1: implication of CpG methylation for most frequent mutations.
    Ophthalmic Genet, 25(4): 247-55. [Abstract] [Full-text]
14. Mutation analysis of KIF21A in congenital fibrosis of the extraocular muscles (CFEOM) patients.
    Ophthalmic Genet, 25(4): 241-6. [Abstract] [Full-text]
15. Incidence and treatment of diaphragmatic paralysis after cardiac surgery in children.
    Eur J Cardiothorac Surg, 27(1): 53-7. [Abstract] [Full-text]
16. Potent and specific antitumor efficacy of CMC-544, a CD22-targeted immunoconjugate of calicheamicin, against systemically disseminated B-cell lymphoma.
    Clin Cancer Res, 10(24): 8620-9. [Abstract] [Full-text]
17. Absence of the interstitial cells of Cajal in patients with gastroparesis and correlation with clinical findings.
    J Gastrointest Surg, 9(1): 102-8. [Abstract] [Full-text]

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