Scoliosis Research Today is a free monthly online journal that collates and summarizes the latest research about Scoliosis, including details on treatment, exercises, surgery, symtpoms.

Volume 1 (2005), Issue 10 (October)

1. Preoperative predictors of prolonged postoperative mechanical ventilation in children following scoliosis repair.
   Pediatr Pulmonol, 40(5): 414-9. [Abstract] [Full-text]
2. Simultaneous anterior-posterior approach through a costotransversectomy for the treatment of congenital kyphosis and acquired kyphoscoliotic deformities.
   J Bone Joint Surg Am, 87(10): 2281-9. [Abstract] [Full-text]
3. An analysis of PAX1 in the development of vertebral malformations.
   Clin Genet, 68(5): 448-53. [Abstract] [Full-text]
4. Teratogenic effects in rabbits of simultaneous exposure to ochratoxin A and aflatoxin B1 with special reference to microscopic effects.
   Toxicology, 215(1): 37-47. [Abstract] [Full-text]
5. Primary thoracoplasty and pedicle screw instrumentation in thoracic idiopathic scoliosis.
   Eur Spine J, 14(8): 777-82. [Abstract] [Full-text]
6. Morphological study of rib regeneration following costectomy in adolescent idiopathic scoliosis.
   Eur Spine J, 14(8): 772-6. [Abstract] [Full-text]
7. Late-onset spinal deformities in children treated by laminectomy and radiation therapy for malignant tumours.
   Eur Spine J, 14(8): 765-71. [Abstract] [Full-text]
8. Late implant infections caused by Propionibacterium acnes in scoliosis surgery.
   Eur Spine J, 14(8): 783-8. [Abstract] [Full-text]
9. The suprapedicle claw construct in anterior scoliosis surgery.
   Eur Spine J, 14(8): 789-94. [Abstract] [Full-text]
10. Pull-out strength of the suprapedicle claw construct: a biomechanical study.
    Eur Spine J, 14(8): 759-64. [Abstract] [Full-text]
11. The phenotype of short stature homeobox gene (SHOX) deficiency in childhood: contrasting children with Leri-Weill dyschondrosteosis and Turner syndrome.
    J Pediatr, 147(4): 499-507. [Abstract] [Full-text]
12. Cardiac tamponade associated with a peripheral vein central venous catheter.
    Paediatr Anaesth, 15(11): 988-92. [Abstract] [Full-text]
13. Familial Chiari type I malformation with syringomyelia in two siblings: case report and review of the literature.
    Childs Nerv Syst, 21(11): 955-9. [Abstract] [Full-text]
14. Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosis.
    Neuromuscul Disord, 15(11): 764-7. [Abstract] [Full-text]
15. Predictive value of the early clinical signs in Rett disorder.
    Brain Dev, 27: S20-S24. [Abstract] [Full-text]
16. Clinical profile of a male with Rett syndrome.
    Brain Dev, 27: S69-S71. [Abstract] [Full-text]
17. Rett syndrome from a family perspective: The Swedish Rett Center survey.
    Brain Dev, 27: S14-S19. [Abstract] [Full-text]
18. Subtotal amelia in a child with autosomal recessive hypohidrotic ectodermal dysplasia.
    Afr Health Sci, 5(3): 270-275. [Abstract] [Full-text]

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