Search Results

There are 41639 results for: content related to: Novel medical bathing with traditional C hinese herb formula alleviates paraplegia spasticity

  1. You have free access to this content
    Poster Presentations

    Movement Disorders

    Volume 30, Issue S1, June 2015, Pages: S1–S567,

    Version of Record online : 12 JUN 2015, DOI: 10.1002/mds.26295

  2. An Update on the Hereditary Spastic Paraplegias: New Genes and New Disease Models

    Movement Disorders Clinical Practice

    Volume 2, Issue 3, September 2015, Pages: 213–223, Kishore R. Kumar, Nicholas F. Blair and Carolyn M. Sue

    Version of Record online : 2 JUN 2015, DOI: 10.1002/mdc3.12184

  3. You have free access to this content
    Poster Session

    Movement Disorders

    Volume 31, Issue S2, June 2016, Pages: S1–S697,

    Version of Record online : 19 JUN 2016, DOI: 10.1002/mds.26688

  4. You have free access to this content
    Revisiting genotype–phenotype overlap in neurogenetics: Triplet-repeat expansions mimicking spastic paraplegias

    Human Mutation

    Volume 33, Issue 9, September 2012, Pages: 1315–1323, Conceição Bettencourt, Beatriz Quintáns, Raquel Ros, Israel Ampuero, Zuleima Yáñez, Samuel Ignacio Pascual, Justo García de Yébenes and María-Jesús Sobrido

    Version of Record online : 16 JUL 2012, DOI: 10.1002/humu.22148

  5. Molecular Genetics of Hereditary Spastic Paraplegias

    Standard Article

    eLS

    Giuseppe Novelli and Gianmarco Contino

    Published Online : 15 SEP 2009, DOI: 10.1002/9780470015902.a0021451

  6. Spinal implantation of hNT neurons and neuronal precursors: graft survival and functional effects in rats with ischemic spastic paraplegia

    European Journal of Neuroscience

    Volume 20, Issue 9, November 2004, Pages: 2401–2414, Martin Marsala, Osamu Kakinohana, Tony L. Yaksh, Zoltan Tomori, Silvia Marsala and Dasa Cizkova

    Version of Record online : 12 OCT 2004, DOI: 10.1111/j.1460-9568.2004.03702.x

  7. SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V

    Clinical Genetics

    Volume 83, Issue 3, March 2013, Pages: 257–262, E Sánchez-Ferrero, E Coto, C Beetz, J Gámez, AI Corao, M Díaz, J Esteban, E del Castillo, G Moris, J Infante, M Menéndez, SI Pascual-Pascual, A López de Munaín, MJ Garcia-Barcina and V Alvarez

    Version of Record online : 21 MAY 2012, DOI: 10.1111/j.1399-0004.2012.01896.x

  8. Pott's paraplegia: Prognosis and treatment

    British Journal of Surgery

    Volume 22, Issue 88, April 1935, Pages: 769–799, H. J. Seddon

    Version of Record online : 6 DEC 2005, DOI: 10.1002/bjs.1800228813

  9. Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: Analysis of muscle beta 1 syntrophin

    American Journal of Medical Genetics

    Volume 92, Issue 2, 15 May 2000, Pages: 122–127, P. Rocco, M. Vainzof, S.C. Froehner, M.F. Peters, S.K.N. Marie, M.R. Passos-Bueno and M. Zatz

    Version of Record online : 25 APR 2000, DOI: 10.1002/(SICI)1096-8628(20000515)92:2<122::AID-AJMG8>3.0.CO;2-B

  10. You have free access to this content
    Poster Presentations

    Movement Disorders

    Volume 29, Issue S1, May 2014, Pages: S1–S571,

    Version of Record online : 6 JUN 2014, DOI: 10.1002/mds.25914

  11. Paraplegia in Pott's disease, with special reference to the pathology and etiology

    British Journal of Surgery

    Volume 22, Issue 88, April 1935, Pages: 738–768, R. Weeden Butler

    Version of Record online : 6 DEC 2005, DOI: 10.1002/bjs.1800228812

  12. You have free access to this content
    Poster Presentations

    Movement Disorders

    Volume 27, Issue S1, June 2012, Pages: S1–S523,

    Version of Record online : 19 JUN 2012, DOI: 10.1002/mds.25051

  13. Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients

    Clinical Genetics

    Volume 80, Issue 2, August 2011, Pages: 148–160, NA Schlipf, R Schüle, S Klimpe, KN Karle, M Synofzik, J Schicks, O Riess, L Schöls and P Bauer

    Version of Record online : 13 JUN 2011, DOI: 10.1111/j.1399-0004.2011.01715.x

  14. ‘Pure’ and ‘Complicated’ Forms of Hereditary Spastic Paraplegia Presenting in Childhood

    Developmental Medicine & Child Neurology

    Volume 33, Issue 4, April 1991, Pages: 304–312, R. E. Appleton, K. Farrell and H. G. Dunn

    Version of Record online : 12 NOV 2008, DOI: 10.1111/j.1469-8749.1991.tb14881.x

  15. Further evidence for a fourth gene causing X-linked pure spastic paraplegia

    American Journal of Medical Genetics

    Volume 111, Issue 2, 1 August 2002, Pages: 152–156, A. Starling, P. Rocco, F. Cambi, G.M. Hobson, M.R. Passos Bueno and M. Zatz

    Version of Record online : 13 JUN 2002, DOI: 10.1002/ajmg.10551

  16. Perceptual weighting of pain behaviours of others, not information integration, varies with expertise

    European Journal of Pain

    Volume 18, Issue 1, January 2014, Pages: 110–119, E. Prigent, M.-A. Amorim, P. Leconte and D. Pradon

    Version of Record online : 2 JUL 2013, DOI: 10.1002/j.1532-2149.2013.00354.x

  17. You have free access to this content
    Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus

    Human Mutation

    Volume 23, Issue 1, January 2004, Page: 98, S.M. Sauter, W. Engel, L.M. Neumann, J. Kunze and J. Neesen

    Version of Record online : 19 DEC 2003, DOI: 10.1002/humu.9205

  18. Botulinum neurotoxin type A injections reduce spasticity in mild to moderate hereditary spastic paraplegia— Report of 19 cases

    Movement Disorders

    Volume 23, Issue 2, 30 January 2008, Pages: 228–233, Martin J. Hecht, Henning Stolze, Matthias Auf Dem Brinke, Ralf Giess, Thoams Treig, Martin Winterholler, Jörg Wissel and German Spasticity Education Group

    Version of Record online : 12 NOV 2007, DOI: 10.1002/mds.21809

  19. Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations

    Clinical Genetics

    Volume 81, Issue 2, February 2012, Pages: 150–157, A Arnoldi, C Crimella, E Tenderini, A Martinuzzi, MG D'Angelo, O Musumeci, A Toscano, M Scarlato, M Fantin, N Bresolin and MT Bassi

    Version of Record online : 31 JAN 2011, DOI: 10.1111/j.1399-0004.2011.01624.x

  20. You have full text access to this OnlineOpen article
    AP5Z1/SPG48 frequency in autosomal recessive and sporadic spastic paraplegia

    Molecular Genetics & Genomic Medicine

    Volume 2, Issue 5, September 2014, Pages: 379–382, Nina A. Schlipf, Rebecca Schüle, Sven Klimpe, Kathrin N. Karle, Matthis Synofzik, Julia Wolf, Olaf Riess, Ludger Schöls and Peter Bauer

    Version of Record online : 25 MAY 2014, DOI: 10.1002/mgg3.87