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This issue will cover chiari malformation in both children and adult populations. In the past, it was estimated that the condition occurs in about one in every 1,000 births. However, the increased use of diagnostic imaging has shown that CM may be much more common. Complicating this estimation is the fact that some children who are born with the condition may not show symptoms until adolescence or adulthood, if at all. CMs occur more often in women than in men and Type II malformations are more prevalent in certain groups, including people of Celtic descent.

1. Cover image - p. Cover 2. Title page - p. Cover 3. Table of Contents - p. Cover 4. Copyright - p. Cover 5. Contributors - p. Cover 6. Forthcoming Issues - p. Cover 7. Erratum - p. Cover 8. Preface. Chiari I Malformation: Adult and Pediatric Considerations - p. Cover 9. Definitions and Anatomic Considerations in Chiari I Malformation and Associated Syringomyelia - p. Cover 10. Pathogenesis and Cerebrospinal Fluid Hydrodynamics of the Chiari I Malformation - p. Cover 11. Prevalence of Chiari I Malformation and Syringomyelia - p. Cover 12. Clinical Presentation of Chiari I Malformation and Syringomyelia in Children - p. Cover 13. Clinical Presentation and Alternative Diagnoses in the Adult Population - p. Cover 14. Advanced Imaging of Chiari 1 Malformations - p. Cover 15. Surgical Treatment of Chiari I Malformation - p. Cover 16. Clinical Outcome Measures in Chiari I Malformation - p. Cover 17. Surgical History of Sleep Apnea in Pediatric Patients with Chiari Type 1 Malformation - p. Cover 18. Complex Chiari Malformations in Children: Diagnosis and Management - p. Cover 19. Craniovertebral Junction Instability in the Setting of Chiari I Malformation - p. Cover 20. Ventral Decompression in Chiari Malformation, Basilar Invagination, and Related Disorders - p. Cover 21. Spinal Deformity Associated with Chiari Malformation - p. Cover 22. Index - p. Cover

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Descripcion
Descripción

This issue will cover chiari malformation in both children and adult populations. In the past, it was estimated that the condition occurs in about one in every 1,000 births. However, the increased use of diagnostic imaging has shown that CM may be much more common. Complicating this estimation is the fact that some children who are born with the condition may not show symptoms until adolescence or adulthood, if at all. CMs occur more often in women than in men and Type II malformations are more prevalent in certain groups, including people of Celtic descent.

1. Cover image - p. Cover 2. Title page - p. Cover 3. Table of Contents - p. Cover 4. Copyright - p. Cover 5. Contributors - p. Cover 6. Forthcoming Issues - p. Cover 7. Erratum - p. Cover 8. Preface. Chiari I Malformation: Adult and Pediatric Considerations - p. Cover 9. Definitions and Anatomic Considerations in Chiari I Malformation and Associated Syringomyelia - p. Cover 10. Pathogenesis and Cerebrospinal Fluid Hydrodynamics of the Chiari I Malformation - p. Cover 11. Prevalence of Chiari I Malformation and Syringomyelia - p. Cover 12. Clinical Presentation of Chiari I Malformation and Syringomyelia in Children - p. Cover 13. Clinical Presentation and Alternative Diagnoses in the Adult Population - p. Cover 14. Advanced Imaging of Chiari 1 Malformations - p. Cover 15. Surgical Treatment of Chiari I Malformation - p. Cover 16. Clinical Outcome Measures in Chiari I Malformation - p. Cover 17. Surgical History of Sleep Apnea in Pediatric Patients with Chiari Type 1 Malformation - p. Cover 18. Complex Chiari Malformations in Children: Diagnosis and Management - p. Cover 19. Craniovertebral Junction Instability in the Setting of Chiari I Malformation - p. Cover 20. Ventral Decompression in Chiari Malformation, Basilar Invagination, and Related Disorders - p. Cover 21. Spinal Deformity Associated with Chiari Malformation - p. Cover 22. Index - p. Cover

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