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Expert Opinion on Pharmacotherapy Volume 7, 2006 - Issue 14
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Editorial

Hereditary spastic paraplegia: clinical genomics and pharmacogenetic perspectives

Gianmarco Contino Resident, Department of Biopathology and Diagnostic Imaging, Tor Vergata University of Rome, V.le Oxford, 81, 00133 Rome, Italy
&
Giuseppe Novelli Professor of Human Genetics, Department of Biopathology and Diagnostic Imaging, Tor Vergata University of Rome, V.le Oxford, 81, 00133 Rome, Italy. [email protected]
Pages 1849-1856 | Published online: 04 Oct 2006

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Jessie Khera, Nadine E Andrew, Dominique A Cadilhac, Tara Purvis, Michael C Fahey & Hyam Barry Rawicki. (2015) Use of continuous intrathecal baclofen in hereditary spastic paraplegia. Clinical Audit 7, pages 19-26.
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Articles from other publishers (7)

Laurene A. Sweet, Lindsey M. O'Neill & Matthew B. Dobbs. (2014) Serial Casting for Neuromuscular Flatfoot and Vertical Talus in an Adolescent With Hereditary Spastic Paraplegia. Pediatric Physical Therapy 26:2, pages 253-264.
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Jian Zeng, Yanhong Lin, Aizhen Yan, Longfeng Ke, Zhongyong Zhu & Fenghua Lan. (2011) Establishment of a Molecular Diagnostic System for Spinal Muscular Atrophy. The Journal of Molecular Diagnostics 13:1, pages 41-47.
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Laura Southgate, Dimitra Dafou, Jacqueline Hoyle, Nan Li, Esther Kinning, Peter Critchley, Andrea H. Németh, Kevin Talbot, Parayil S. Bindu, Sanjib Sinha, Arun B. Taly, Seetharam Raghavendra, Ferenc Müller, Eamonn R. Maher & Richard C. Trembath. (2010) Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish. neurogenetics 11:4, pages 379-389.
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Christine Albertyn, Sean O'Dowd, John McHugh & Raymond Murphy. (2010) Compliance with McDonald criteria and red flag recognition in a general neurology practice in Ireland. Multiple Sclerosis Journal 16:6, pages 678-684.
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David Pountney. (2010) Identifying and managing hereditary spastic paraplegia. British Journal of Neuroscience Nursing 6:4, pages 173-175.
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Jonathon L. Burman, Lyne Bourbonniere, Jacynthe Philie, Thomas Stroh, Selma Y. Dejgaard, John F. Presley & Peter S. McPherson. (2008) Scyl1, Mutated in a Recessive Form of Spinocerebellar Neurodegeneration, Regulates COPI-mediated Retrograde Traffic. Journal of Biological Chemistry 283:33, pages 22774-22786.
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T. WarneckeT. DuningA. SchwanH. LohmannJ. T. EpplenP. Young. (2007) A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation . Neurology 69:4, pages 368-375.
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