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Relevant bibliographies by topics / Spinal Dysraphism Spinal Dysraphism / Books

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Books on the topic 'Spinal Dysraphism Spinal Dysraphism'

Author: Grafiati

Published: 4 June 2021

Last updated: 13 February 2022

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1

Tubbs, R. Shane, Rod J. Oskouian, Jeffrey P. Blount, and W. Jerry Oakes, eds. Occult Spinal Dysraphism. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-10994-3.

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2

L, Seljeskog Edward, ed. A parent's guide to spina bifida. University of Minnesota Press, 1988.

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3

Sandler, Adrian. Living with spina bifida: A guide for families and professionals. University of North Carolina Press, 1997.

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4

Sandler, Adrian. Living with spina bifida: A guide for families and professionals. University of North Carolina Press, 2004.

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5

Tanni. CollinsWillow, 1996.

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6

S, Park T., ed. Spinal dysraphism. Blackwell Scientific Publications, 1993.

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7

Dachling, Pang, ed. Spinal dysraphism. Saunders, 1995.

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8

Tubbs, R. Shane, W. Jerry Oakes, Rod J. Oskouian, and Jeffrey P. Blount. Occult Spinal Dysraphism. Springer, 2019.

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9

Park, Therese S. Spinal Dysraphism (Contemporary Issues in Neurological Surgery). Blackwell Science Inc, 1992.

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10

Kinsman, Stephen L. Spina Bifida and Related Conditions. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0077.

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The term “spinal dysraphism” encompasses the broadest array of the conditions known as the neural tube defects. The open neural tube defects (spina bifida aperta and cystica) include both disorders of primary and/or secondary neuralation and are best defined as myelomeningocele complex (MMC) due to their protean nervous system manifestations beyond the spinal lesion. Closed spinal dysraphisms (so-called spina bifida occulta) include lipomatous lesions, forms of tethered spinal cord, sinus tracts, and forms of split spinal cord (diastematomyelia). Both genetic and environmental etiologies have

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11

Seljeskog, Edward L., and Beth-Ann Bloom. Parent's Guide to Spina Bifida. University of Minnesota Press, 1988.

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12

Hoang, Jimmy, and Samuel David Yanofsky. Neural Tube Defects. Edited by Kirk Lalwani, Ira Todd Cohen, Ellen Y. Choi, and Vidya T. Raman. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190685157.003.0025.

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Neural tube defects (NTDs) are congenital abnormalities that arise from the neural tube failing to close. These defects can affect the brain, spine, or spinal cord and generally happen within the first month of pregnancy. Cranial dysraphism is failure of cranial neural tube closure and includes anencephaly and encephalocele. Spinal dysraphism is failure of caudal neuropore closure and includes spina bifida cystica and occulta. Myelomeningocele is a type of spina bifida cystica where the membranous sac containing neural tissue protrudes through an opening in the back. It is the most common NTD

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13

Travis, Karen Snyder. Christal: Coping With Spina Bifida. Branden Books, 2001.

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14

Neural Tube Defects (Pediatric Habilitation). Informa Healthcare, 2007.

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15

Neural tube defects. Informa Healthcare USA, 2007.

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16

Rinaldi, Simon. Congenital neurological disorders. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0225.

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This chapter covers four congenital neurological disorders which may be encountered in adult medicine: cerebral palsy, Chiari malformations, spina bifida, and tethered cord syndromes. Cerebral palsy is a disturbance of motor function arising from damage to the developing fetal or infant brain. It usually refers to a disorder resulting from a non-progressive insult which occurred at less than 3 years of age. Chiari malformations are congenital abnormalities of the anatomy and structural relationships of the cerebellum, the brainstem, and the foramen magnum. Dysraphism is a failure of opposition

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17

(Editor), Memet Ozek, Giuseppe Cinalli (Editor), and Wirginia June Maixner (Editor), eds. Spina Bifida: Management and Outcome. Springer, 2008.

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18

Sandler, Adrian. Living with Spina Bifida: A Guide for Families and Professionals. University of North Carolina Press, 2009.

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19

Sandler, Adrian. Living with Spina Bifida: A Guide for Families and Professionals. University of North Carolina Press, 2009.

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20

(Editor), Carys M. Bannister, and Brian Tew (Editor), eds. Current Concepts in Spina Bifida and Hydrocephalus (Clinics in Developmental Medicine (Mac Keith Press)). Cambridge University Press, 1992.

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21

M, Bannister Carys, and Tew Brian, eds. Current concepts in spina bifida and hydrocephalus. Mac Keith Press, 1991.

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22

Bannister, Carys M., and Brian Tew. Current Concepts in Spina Bifida and Hydrocephalus (Clinics in Developmental Medicine). MacKeith Press, 1993.

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23

M, Bannister Carys, Tew Brian, and Spastics Society, eds. Current concepts in spina bifida and hydrocephalus. MacKeith Press, 1991.

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24

Kowal, Deborah. The China-US Partnership to Prevent Spina Bifida: The Evolution of a Landmark Epidemiological Study. Vanderbilt University Press, 2015.

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25

Kowal, Deborah. China-US Partnership to Prevent Spina Bifida: The Evolution of a Landmark Epidemiological Study. Vanderbilt University Press, 2015.

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26

Farooq, Najma, S. K. Tucker, and D. Thompson. Neurological aspects of spinal disorders in children. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199550647.003.013008.

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♦ Spinal neurological problems may be a focal anomaly or part of a systemic disorder♦ The neuro-orthopaedic syndrome should be considered in any dysraphic patient with a changing clinical picture—urological symptoms respond well to prompt untethering♦ Ten per cent of central nervous system tumours originate in the spinal cord—they may be intramedullary, intradural extramedullary, or extradural.

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27

Raimondi, Anthony J., and Maurice Choux. The Pediatric Spine I: Development and the Dysraphic State (Principles of Pediatric Neurosurgery). Springer, 1989.

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