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There are 2617 results for: content related to: Myopathy causing camptocormia in idiopathic Parkinson's disease: A multidisciplinary approach

  1. You have free access to this content
    EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders

    European Journal of Neurology

    Volume 18, Issue 2, February 2011, Pages: 207–217, J.-M. Burgunder, L. Schöls, J. Baets, P. Andersen, T. Gasser, Z. Szolnoki, B. Fontaine, C. Van Broeckhoven, S. Di Donato, P. De Jonghe, T. Lynch, C. Mariotti, A. Spinazzola, S. J. Tabrizi, C. Tallaksen, M. Zeviani, H. F. Harbo and J. Finsterer

    Version of Record online : 25 MAY 2010, DOI: 10.1111/j.1468-1331.2010.03069.x

  2. Review of X-linked syndromes with arthrogryposis or early contractures—aid to diagnosis and pathway identification

    American Journal of Medical Genetics Part A

    Volume 167, Issue 5, May 2015, Pages: 931–973, Jesse M. Hunter, Jeff Kiefer, Christopher D. Balak, Sonya Jooma, Mary Ellen Ahearn, Judith G. Hall and Lisa Baumbach-Reardon

    Version of Record online : 19 MAR 2015, DOI: 10.1002/ajmg.a.36934

  3. Needle electromyography

    Muscle & Nerve

    Volume 39, Issue 2, February 2009, Pages: 244–270, Jasper R. Daube and Devon I. Rubin

    Version of Record online : 14 JAN 2009, DOI: 10.1002/mus.21180

  4. Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 6, 15 March 2008, Pages: 745–757, Virginia. E. Kimonis, Sarju G. Mehta, Erin C. Fulchiero, Dana Thomasova, Marzia Pasquali, Kym Boycott, Edward G. Neilan, Alex Kartashov, Mark S. Forman, Stuart Tucker, Katerina Kimonis, Steven Mumm, Michael P. Whyte, Charles D. Smith and Giles D. J. Watts

    Version of Record online : 7 FEB 2008, DOI: 10.1002/ajmg.a.31862

  5. A novel autosomal dominant distal myopathy with early respiratory failure: Clinico-pathologic characteristics and exclusion of linkage to candidate genetic loci

    Annals of Neurology

    Volume 49, Issue 4, April 2001, Pages: 443–452, Patrick F. Chinnery, Margaret A. Johnson, Timothy J. Walls, G. John Gibson, Peter R. W. Fawcett, Sarra Jamieson, John J. Fulthorpe, Michael Cullen, Peter Hudgson and Kate M. D. Bushby

    Version of Record online : 2 APR 2001, DOI: 10.1002/ana.93

  6. Histopathological differences between human T-lymphotropic virus type 1-positive and human T-lymphotropic virus type 1-negative polymyositis

    Clinical and Experimental Neuroimmunology

    Volume 2, Issue 1, January 2011, Pages: 12–24, Hazem M. Abdullah, Itsuro Higuchi, Ryuji Kubota, Eiji Matsuura, Akihiro Hashiguchi, Nashwa H. Abdelbary, Yukie Inamori, Hiroshi Takashima and Shuji Izumo

    Version of Record online : 27 JAN 2011, DOI: 10.1111/j.1759-1961.2011.00017.x

  7. EFNS review on the role of muscle biopsy in the investigation of myalgia

    European Journal of Neurology

    Volume 20, Issue 7, July 2013, Pages: 997–1005, T. Kyriakides, C. Angelini, J. Schaefer, T. Mongini, G. Siciliano, S. Sacconi, J. Joseph, J. M. Burgunder, L. A. Bindoff, J. Vissing, M. de Visser and D. Hilton-Jones

    Version of Record online : 30 APR 2013, DOI: 10.1111/ene.12174

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    Muscle imaging in inherited and acquired muscle diseases

    European Journal of Neurology

    Volume 23, Issue 4, April 2016, Pages: 688–703, L. ten Dam, A. J. van der Kooi, C. Verhamme, M. P. Wattjes and M. de Visser

    Version of Record online : 18 MAR 2016, DOI: 10.1111/ene.12984

  9. Diagnostic value of electromyography and muscle biopsy in arthrogryposis multiplex congenita

    Annals of Neurology

    Volume 54, Issue 6, December 2003, Pages: 790–795, Peter B. Kang, Hart G. W. Lidov, William S. David, Alcy Torres, Douglas C. Anthony, H. Royden Jones and Basil T. Darras

    Version of Record online : 5 NOV 2003, DOI: 10.1002/ana.10769

  10. Clinical and genetic aspects of distal myopathies

    Muscle & Nerve

    Volume 24, Issue 11, November 2001, Pages: 1440–1450, David S. Saperstein, Anthony A. Amato and Richard J. Barohn

    Version of Record online : 18 OCT 2001, DOI: 10.1002/mus.1167

  11. Early disintegration of myonuclear fibrous lamina in inclusion body myositis: Ultrastructural and immunohistochemical studies

    Clinical and Experimental Neuroimmunology

    Volume 7, Issue 2, May 2016, Pages: 185–196, Shiro Matsubara, Koichi Kondo, Kazuhito Miyamoto, Akihiro Kawata, Takashi Komori and Imaharu Nakano

    Version of Record online : 1 FEB 2016, DOI: 10.1111/cen3.12287

  12. Mitochondriopathies

    European Journal of Neurology

    Volume 11, Issue 3, March 2004, Pages: 163–186, J. Finsterer

    Version of Record online : 4 MAR 2004, DOI: 10.1046/j.1351-5101.2003.00728.x

  13. Open muscle biopsy in suspected myopathy: diagnostic yield and clinical utility

    European Journal of Neurology

    Volume 17, Issue 1, January 2010, Pages: 136–142, C.-H. Lai, G. Melli, Y.-J. Chang, R. L. Skolasky, A. M. Corse, K. R. Wagner and D. R. Cornblath

    Version of Record online : 5 AUG 2009, DOI: 10.1111/j.1468-1331.2009.02765.x

  14. Abnormal blood lactate accumulation after exercise in patients with multiple mitochondrial DNA deletions and minor muscular symptoms

    Clinical Physiology and Functional Imaging

    Volume 24, Issue 2, March 2004, Pages: 109–115, Harri Lindholm, Mervi Löfberg, Hannu Somer, Hannu Näveri and Anssi Sovijärvi

    Version of Record online : 22 MAR 2004, DOI: 10.1111/j.1475-097X.2004.00531.x

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    Congenital myopathies – a comprehensive update of recent advancements

    Acta Neurologica Scandinavica

    Volume 119, Issue 5, May 2009, Pages: 281–292, M. C. Sharma, D. Jain, C. Sarkar and H. H. Goebel

    Version of Record online : 30 DEC 2008, DOI: 10.1111/j.1600-0404.2008.01126.x

  16. Further delineation of FKBP14-related Ehlers–Danlos syndrome: A patient with early vascular complications and non-progressive kyphoscoliosis, and literature review

    American Journal of Medical Genetics Part A

    Chiara Dordoni, Claudia Ciaccio, Marina Venturini, Piergiacomo Calzavara-Pinton, Marco Ritelli and Marina Colombi

    Version of Record online : 5 MAY 2016, DOI: 10.1002/ajmg.a.37728

  17. Adult-onset glycogen storage disease type 2: clinico-pathological phenotype revisited

    Neuropathology and Applied Neurobiology

    Volume 33, Issue 5, October 2007, Pages: 544–559, B. G. H. Schoser, J. Müller-Höcker, R. Horvath, K. Gempel, D. Pongratz, H. Lochmüller and W. Müller-Felber

    Version of Record online : 15 JUN 2007, DOI: 10.1111/j.1365-2990.2007.00839.x

  18. Anesthetic management of 877 pediatric patients undergoing muscle biopsy for neuromuscular disorders: a 20-year review

    Pediatric Anesthesia

    Volume 26, Issue 7, July 2016, Pages: 710–721, Frederic Shapiro, Umeshkumar Athiraman, David J. Clendenin, Monica Hoagland and Navil F. Sethna

    Version of Record online : 25 APR 2016, DOI: 10.1111/pan.12909

  19. Limb girdle muscular dystrophy: use of dHPLC and direct sequencing to detect sarcoglycan gene mutations in a New Zealand cohort

    Clinical Genetics

    Volume 65, Issue 1, January 2004, Pages: 55–60,

    Version of Record online : 10 DEC 2003, DOI: 10.1111/j..2004.00193.x

  20. You have free access to this content
    Chronic intestinal pseudo-obstruction: manifestations, natural history and management

    Neurogastroenterology & Motility

    Volume 19, Issue 6, June 2007, Pages: 440–452, V. Stanghellini, R. F. Cogliandro, R. De Giorgio, G. Barbara, B. Salvioli and R. Corinaldesi

    Version of Record online : 13 MAR 2007, DOI: 10.1111/j.1365-2982.2007.00902.x