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There are 61494 results for: content related to: Patient with adult-onset congenital neuromuscular disease with uniform type 1 fibers

  1. Adult onset pigmentary orthochromatic leukodystrophy with ovarian dysgenesis

    European Journal of Neurology

    Volume 9, Issue 6, November 2002, Pages: 663–670, J. Verghese, K. Weidenheim, S. Malik and I. Rapin

    Version of Record online : 9 DEC 2002, DOI: 10.1046/j.1468-1331.2002.00469.x

  2. A family with autosomal dominant leukodystrophy linked to 5q23.2–q23.3 without lamin B1 mutations

    European Journal of Neurology

    Volume 17, Issue 4, April 2010, Pages: 541–549, A. Brussino, G. Vaula, C. Cagnoli, E. Panza, M. Seri, E. Di Gregorio, S. Scappaticci, S. Camanini, D. Daniele, G. B. Bradac, L. Pinessi, S. Cavalieri, E. Grosso, N. Migone and A. Brusco

    Version of Record online : 4 DEC 2009, DOI: 10.1111/j.1468-1331.2009.02844.x

  3. 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

  4. Adult-onset Alexander disease with palatal myoclonus and intraventricular tumour

    European Journal of Neurology

    Volume 15, Issue 2, February 2008, Pages: e16–e17, T. Hirayama, J. Fukae, K. Noda, K. Fujishima, T. Yamamoto, K. Mori, M. Maeda, N. Hattori, N. Shiroma, S. Tsurui and Y. Okuma

    Version of Record online : 21 JAN 2008, DOI: 10.1111/j.1468-1331.2007.02031.x

  5. You have full text access to this Open Access content
    Nemaline Rods in Canine Myopathies: 4 Case Reports and Literature Review

    Journal of Veterinary Internal Medicine

    Volume 12, Issue 6, November 1998, Pages: 424–430, Agnes J. Delauche, Paul A. Cuddon, Michael Podell, Kim Devoe, Henry C. Powell and G. Diane Shelton

    Version of Record online : 5 FEB 2008, DOI: 10.1111/j.1939-1676.1998.tb02145.x

  6. Characterization of the Asian myopathy patients with VCP mutations

    European Journal of Neurology

    Volume 19, Issue 3, March 2012, Pages: 501–509, Z. Shi, Y. K. Hayashi, S. Mitsuhashi, K. Goto, D. Kaneda, Y.-C. Choi, C. Toyoda, S. Hieda, T. Kamiyama, H. Sato, M. Wada, S. Noguchi, I. Nonaka and I. Nishino

    Version of Record online : 31 OCT 2011, DOI: 10.1111/j.1468-1331.2011.03575.x

  7. A prospective, open-label treatment trial to compare the effect of IFN β-1a (Avonex), IFNβ-1b (Betaseron), and glatiramer acetate (Copaxone) on the relapse rate in relapsing-remitting multiple sclerosis

    European Journal of Neurology

    Volume 8, Issue 2, March 2001, Pages: 141–148, O. A. Khan, A. C. Tselis, J. A. Kamholz, J. Y. Garbern, R. A. Lewis and R. P. Lisak

    Version of Record online : 7 JUL 2008, DOI: 10.1046/j.1468-1331.2001.00189.x

  8. Outcome measures of spasticity

    European Journal of Neurology

    Volume 9, Issue s1, May 2002, Pages: 10–16, G. R. Johnson

    Version of Record online : 25 MAR 2002, DOI: 10.1046/j.1468-1331.2002.0090s1010.x

  9. Natural history of Crohn's disease: Comparison between childhood- and adult-onset disease

    Inflammatory Bowel Diseases

    Volume 16, Issue 6, June 2010, Pages: 953–961, Bénédicte Pigneur, Philippe Seksik, Sheila Viola, Jérôme Viala, Laurent Beaugerie, Jean-Philippe Girardet, Frank M. Ruemmele and Jacques Cosnes

    Version of Record online : 15 OCT 2009, DOI: 10.1002/ibd.21152

  10. The 40-mg dose of eletriptan: comparative efficacy and tolerability versus sumatriptan 100 mg

    European Journal of Neurology

    Volume 11, Issue 2, February 2004, Pages: 125–134, Hans-Christoph Diener, Robert Ryan, Wei Sun and Jayasena Hettiarachchi

    Version of Record online : 28 JAN 2004, DOI: 10.1046/j.1351-5101.2003.00730.x

  11. Pure quadriceps myopathy in two sisters

    European Journal of Neurology

    Volume 10, Issue 4, July 2003, Pages: 453–456, I. Mahjneh, H. Somer, A. Paetau and G. Marconi

    Version of Record online : 19 JUN 2003, DOI: 10.1046/j.1468-1331.2003.00616.x

  12. Cost of disorders of the brain in Europe

    European Journal of Neurology

    Volume 12, Issue s1, June 2005, Pages: 1–27, Patrik Andlin-Sobocki, Bengt Jönsson, Hans-Ulrich Wittchen and Jes Olesen

    Version of Record online : 5 MAY 2005, DOI: 10.1111/j.1468-1331.2005.01202.x

  13. Juvenile-onset neuronal ceroid lipofuscinosis with infantile CLN1 mutation and palmitoyl-protein thioesterase deficiency

    European Journal of Neurology

    Volume 14, Issue 4, April 2007, Pages: 369–372, R. Kälviäinen, K. Eriksson, M. Losekoot, I. Sorri, I. Harvima, P. Santavuori, I. Järvelä, T. Autti, R. Vanninen, T. Salmenperä and O. P. Van Diggelen

    Version of Record online : 23 MAR 2007, DOI: 10.1111/j.1468-1331.2007.01668.x

  14. Late-onset vanishing white matter disease with compound heterozygous EIF2B5 gene mutations

    European Journal of Neurology

    Volume 16, Issue 3, March 2009, Pages: e42–e43, H.-N. Lee, S.-H. Koh, K.-Y. Lee, C.-S. Ki and Y. J. Lee

    Version of Record online : 23 DEC 2008, DOI: 10.1111/j.1468-1331.2008.02395.x

  15. Acute onset of fatal vegetative symptoms: unusual presentation of adult Alexander disease

    European Journal of Neurology

    Volume 14, Issue 11, November 2007, Pages: 1251–1255, H. B. Huttner, G. Richter, M. Hildebrandt, I. Blümcke, T. Fritscher, W. Brück, J. Gärtner, F. Seifert, D. Staykov, M.-J. Hilz, S. Schwab and J. Bardutzky

    Version of Record online : 19 OCT 2007, DOI: 10.1111/j.1468-1331.2007.01961.x

  16. Multiple sclerosis in Oslo, Norway: prevalence on 1 January 1995 and incidence over a 25-year period

    European Journal of Neurology

    Volume 8, Issue 5, September 2001, Pages: 463–469, E. G. Celius and B. Vandvik

    Version of Record online : 21 DEC 2001, DOI: 10.1046/j.1468-1331.2001.00269.x

  17. Disorders in intentional gestural organization in Alzheimer’s disease: combined or selective impairment of the conceptual and production systems?

    European Journal of Neurology

    Volume 8, Issue 6, November 2001, Pages: 629–641, A. Blondel, B. Desgranges, V. De La Sayette, S. Schaeffer, K. Benali, B. Lechevalier, F. Viader and F. Eustache

    Version of Record online : 21 DEC 2001, DOI: 10.1046/j.1468-1331.2001.00318.x

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    Skeletal muscle development in normal and double-muscled cattle

    The Anatomical Record Part A: Discoveries in Molecular, Cellular, and Evolutionary Biology

    Volume 281A, Issue 2, December 2004, Pages: 1363–1371, Julie K. Martyn, John J. Bass and Jenny M. Oldham

    Version of Record online : 5 NOV 2004, DOI: 10.1002/ar.a.20140

  19. CADASIL syndrome in a large Turkish kindred caused by the R90C mutation in the Notch3 receptor

    European Journal of Neurology

    Volume 9, Issue 1, January 2002, Pages: 23–28, U. Utku, Y. Celik, O. Uyguner, M. Yüksel-Apak and B. Wollnik

    Version of Record online : 11 JAN 2002, DOI: 10.1046/j.1468-1331.2002.00344.x

  20. The role of genes in causing dystonia

    European Journal of Neurology

    Volume 17, Issue s1, July 2010, Pages: 65–70, A. Schmidt and C. Klein

    Version of Record online : 8 JUN 2010, DOI: 10.1111/j.1468-1331.2010.03055.x