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There are 2788621 results for: content related to: Methylphenidate fails to improve gait and muscle tone in patients with sporadic and hereditary spastic paraplegia

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    A Family with Hereditary Spastic Paraparesis and Epilepsy

    Epilepsia

    Volume 38, Issue 4, April 1997, Pages: 495–499, Stewart Webb, Niamh Flanagan, Noel Callaghan and Michael Hutchinson

    Article first published online : 3 AUG 2005, DOI: 10.1111/j.1528-1157.1997.tb01741.x

  2. Hereditary spastic paraplegia with neurogenic bladder disturbances and syndactylia

    Acta Neurologica Scandinavica

    Volume 61, Issue 1, January 1980, Pages: 35–41, Stein Opjordsmoen and Rolf Nyberg-Hansen

    Article first published online : 29 JAN 2009, DOI: 10.1111/j.1600-0404.1980.tb02993.x

  3. Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia

    Clinical Genetics

    Volume 79, Issue 6, June 2011, Pages: 523–530, DS McCorquodale III, U Ozomaro, J Huang, G Montenegro, A Kushman, L Citrigno, J Price, F Speziani, MA Pericak-Vance and S Züchner

    Article first published online : 2 JUL 2010, DOI: 10.1111/j.1399-0004.2010.01501.x

  4. Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia

    Human Mutation

    Volume 20, Issue 2, August 2002, Pages: 127–132, S. Sauter, B. Miterski, S. Klimpe, D. Bönsch, L. Schöls, A. Visbeck, T. Papke, H.C. Hopf, W. Engel, T. Deufel, J.T. Epplen and J. Neesen

    Article first published online : 16 JUL 2002, DOI: 10.1002/humu.10105

  5. Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity

    Clinical Genetics

    Volume 75, Issue 6, June 2009, Pages: 527–536, A Boukhris, G Stevanin, I Feki, P Denora, N Elleuch, MI Miladi, C Goizet, J Truchetto, S Belal, A Brice and C Mhiri

    Article first published online : 5 MAY 2009, DOI: 10.1111/j.1399-0004.2009.01176.x

  6. Hereditary spastic paraparesis with dementia, amyotrophy and peripheral neuropathy. A neuropathological study

    Neuropathology and Applied Neurobiology

    Volume 21, Issue 3, June 1995, Pages: 255–261, I. Ferrer, M. Olive, R. Rivera, A. Pou, B. Narberhaust and A. Ugartet

    Article first published online : 12 MAY 2008, DOI: 10.1111/j.1365-2990.1995.tb01057.x

  7. Prenatal diagnosis of hereditary spastic paraplegia

    Prenatal Diagnosis

    Volume 21, Issue 3, March 2001, Pages: 202–206, Peter Hedera, Jeffrey A. Williamson, Shirley Rainier, David Alvarado, Turgut Tukel, Memnune Apak and John K. Fink

    Article first published online : 16 FEB 2001, DOI: 10.1002/1097-0223(200103)21:3<202::AID-PD4>3.0.CO;2-U

  8. A Dutch family with autosomal dominant pure spastic paraparesis (Strümpell's disease)

    Acta Neurologica Scandinavica

    Volume 82, Issue 3, September 1990, Pages: 169–173, P. Scheltens, R. P. M. Bruyn and G. J. Hazenberg

    Article first published online : 29 JAN 2009, DOI: 10.1111/j.1600-0404.1990.tb04484.x

  9. Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive Parkinsonism

    Movement Disorders

    Volume 26, Issue 3, 15 February 2011, Pages: 553–556, Arianna Guidubaldi, Carla Piano, Filippo M. Santorelli, Gabriella Silvestri, Martina Petracca, Alessandra Tessa and Anna Rita Bentivoglio

    Article first published online : 4 MAR 2011, DOI: 10.1002/mds.23552

  10. Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33–q34

    Annals of Neurology

    Volume 51, Issue 6, June 2002, Pages: 681–685, Enza Maria Valente, Francesco Brancati, Viviana Caputo, Enrico Bertini, Clarice Patrono, Danilo Costanti and Bruno Dallapiccola

    Article first published online : 21 MAY 2002, DOI: 10.1002/ana.10204

  11. Severe resting clonus caused by thyrotoxicosis in a 16-year-old girl with hereditary spastic paraparesis: A case report

    Movement Disorders

    Volume 19, Issue 6, June 2004, Pages: 712–713, Terence D. Sanger

    Article first published online : 21 JAN 2004, DOI: 10.1002/mds.20015

  12. Large deletion involving the 5′-UTR in the spastin gene caused mild phenotype of autosomal dominant hereditary spastic paraplegia

    American Journal of Medical Genetics Part A

    Volume 133A, Issue 1, 15 February 2005, Pages: 13–17, Hiroshi Iwanaga, Akira Tsujino, Susumu Shirabe, Hiroto Eguchi, Naomi Fukushima, Norio Niikawa, Koh-ichiro Yoshiura and Katsumi Eguchi

    Article first published online : 6 JAN 2005, DOI: 10.1002/ajmg.a.30510

  13. Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype

    Clinical Genetics

    Volume 75, Issue 5, May 2009, Pages: 485–489, BN Smith, a S Bevan, b C Vance, a P Renwick, c P Wilkinson, d,e C Proukakis, e F Squitieri, f A Berardelli, g TT Warner, e E Reid and b CE Shaw a,c

    Article first published online : 28 APR 2009, DOI: 10.1111/j.1399-0004.2009.01184.x

  14. SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 7, 5 October 2009, Pages: 984–992, Hanna Örlén, Atle Melberg, Raili Raininko, Eva Kumlien, Miriam Entesarian, Per Söderberg, Magnus Påhlman, Niklas Darin, Mårten Kyllerman, Eva Holmberg, Henry Engler, Urban Eriksson and Niklas Dahl

    Article first published online : 4 FEB 2009, DOI: 10.1002/ajmg.b.30928

  15. Distinct novel mutations affecting the same base in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia in two Chinese families

    Human Mutation

    Volume 25, Issue 2, February 2005, Pages: 135–141, Suqin Chen, Chun Song, Hui Guo, Pingyi Xu, Weijun Huang, Yan Zhou, Jiandong Sun, Cai-Xia Li, Yong Du, Xunhua Li, Zhuolin Liu, Deqin Geng, Patrick H. Maxwell, Cheng Zhang and Yiming Wang

    Article first published online : 10 JAN 2005, DOI: 10.1002/humu.20126

  16. A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia

    Human Mutation

    Volume 29, Issue 4, April 2008, Pages: 522–531, Alessia Arnoldi, Alessandra Tonelli, Francesca Crippa, Gaetano Villani, Consiglia Pacelli, Manuela Sironi, Uberto Pozzoli, Maria Grazia D'Angelo, Giovanni Meola, Andrea Martinuzzi, Claudia Crimella, Francesca Redaelli, Chris Panzeri, Alessandra Renieri, Giacomo Pietro Comi, Anna Carla Turconi, Nereo Bresolin and Maria Teresa Bassi

    Article first published online : 16 JAN 2008, DOI: 10.1002/humu.20682

  17. Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci

    American Journal of Medical Genetics

    Volume 102, Issue 1, 22 July 2001, Pages: 68–72, H. Patel, P.E. Hart, T. Warner, I. Allen, H.E. Phillimore, J.R. Silver, N.W. Wood, S. Jeffery, M.A. Patton and A.H. Crosby

    Article first published online : 5 JUL 2001, DOI: 10.1002/1096-8628(20010722)102:1<68::AID-AJMG1411>3.0.CO;2-R

  18. Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity

    European Journal of Neurology

    Volume 16, Issue 1, January 2009, Pages: 121–126, T. Pippucci, E. Panza, E. Pompilii, V. Donadio, A. Borreca, C. Babalini, C. Patrono, R. Zuntini, T. Kawarai, G. Bernardi, R. Liguori, G. Romeo, P. Montagna, A. Orlacchio and M. Seri

    Article first published online : 12 NOV 2008, DOI: 10.1111/j.1468-1331.2008.02367.x

  19. Double-blind crossover trial of gabapentin in SPG4-linked hereditary spastic paraplegia

    European Journal of Neurology

    Volume 14, Issue 6, June 2007, Pages: 663–666, K. H. Scheuer, K. Svenstrup, P. Jennum, B. á Rogvi-Hansen, L. Werdelin, K. Fenger and J. E. Nielsen

    Article first published online : 29 MAY 2007, DOI: 10.1111/j.1468-1331.2007.01812.x

  20. Computerized tomography in hereditary ataxias

    Acta Neurologica Scandinavica

    Volume 58, Issue 2, August 1978, Pages: 81–88, Lene Pedersen and Carsten Gyldensted

    Article first published online : 29 JAN 2009, DOI: 10.1111/j.1600-0404.1978.tb02864.x