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15 articles with title/keywords/abstract containing Dysplasia of spinal cord

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The time of onset of abnormal calcification in spondylometaepiphyseal dysplasia, short limb-abnormal calcification type

Authors: Tüysüz, Beyhan; Gazioğlu, Nurperi; Üngür, Savaş; Aji, Dolly; Türkmen, Seval

Source: Pediatric Radiology, Volume 39, Number 1, January 2009 , pp. 84-89(6)

Publisher: Springer

Brachytelephalangic chondrodysplasia punctata with severe spinal cord compression: report of four new cases

Authors: Garnier, Arnaud; Dauger, Stéphane; Eurin, Danièle; Parisi, Ida; Parenti, Giancarlo; Garel, Catherine; Delbecque, Katy; Baumann, Clarisse

Source: European Journal of Pediatrics, Volume 166, Number 4, April 2007 , pp. 327-331(5)

Publisher: Springer

MR imaging features of craniodiaphyseal dysplasia

Authors: Marden, Franklin; Wippold, Franz

Source: Pediatric Radiology, Volume 34, Number 2, February 2004 , pp. 167-170(4)

Publisher: Springer

Novel alternative splicing of human faciogenital dysplasia 1 gene

Authors: Kumiko Yanagi; Tadashi Kaname; Yasutsugu Chinen; Kenji Naritomi

Source: Congenital Anomalies, Volume 44, Number 3, September 2004 , pp. 137-141(5)

Publisher: Blackwell Publishing

Posterior ataxia-paraparesis syndrome in the large-breed dog.

Authors: Polizopoulou, Z.S.; Koutinas, A.F.; Koutinas, C.K.

Source: Journal of the Hellenic Veterinary Medical Society, Volume 53, Number 2, April 2002 , pp. 119-131(13)

Publisher: Hellenic Veterinary Medical Society

Friedreich ataxia with minimal GAA expansion presenting as adult-onset spastic ataxia

Authors: Berciano J.; Mateo I.; De Pablos C.; Polo J.M.; Combarros O.

Source: Journal of the Neurological Sciences, Volume 194, Number 1, 15 February 2002 , pp. 75-82(8)

Publisher: Elsevier

Improvement in daily activities using a portable ventilator in a patient with spondyloepiphyseal dysplasia congenita

Authors: Asano, T; Enokido, H; Fujino, O; Hashimoto, K

Source: Pediatrics International, Volume 43, Number 3, June 2001 , pp. 316-318(3)

Publisher: Blackwell Publishing

A Spontaneous Mouse Mutation, mesenchymal dysplasia (mes), Is Caused by a Deletion of the Most C-Terminal Cytoplasmic Domain of patched (ptc)

Authors: Makino S.; Masuya H.; Ishijima J.; Yada Y.; Shiroishi T.

Source: Developmental Biology, Volume 239, Number 1, 1 November 2001 , pp. 95-106(12)

Publisher: Elsevier

A Spontaneous Mouse Mutation, mesenchymal dysplasia (mes), Is Caused by a Deletion of the Most C-Terminal Cytoplasmic Domain of patched (ptc)

Authors: Makino S.; Masuya H.; Ishijima J.; Yada Y.; Shiroishi T.

Source: Developmental Biology, Volume 239, Number 1, November 2001 , pp. 95-106(12)

Publisher: Academic Press

Progressive myelopathy and neuropathy in New Zealand Huntaway dogs

Authors: Jolly R.D.; Burbidge H.M.; Alley M.R.; Pack R.J.; Wilson M.S.

Source: New Zealand Veterinary Journal, Volume 48, Number 6, 1 December 2000 , pp. 188-191(4)

Publisher: New Zealand Veterinary Association

Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy

Authors: Yamamoto T.; Toyoda C.; Kobayashi M.; Kondo E.; Saito K.; Osawa M.

Source: Brain and Development, Volume 19, Number 1, January 1997 , pp. 35-42(8)

Publisher: Elsevier

Spinal epidural hematoma progressing to brown-sequard syndrome: report of a case

Authors: Hancock J.B.; Field E.M.; Gadam R.

Source: Journal of Emergency Medicine, Volume 15, Number 3, May 1997 , pp. 309-312(4)

Publisher: Elsevier

Neurodysraphic state

Author: Huber Z.

Source: Clinical Neurology and Neurosurgery, Volume 99, Supplement 1, July 1997 , pp. 207-207(1)

Publisher: Elsevier

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