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There are 719146 results for: content related to: Congenital myasthenic syndrome and minicore-like myopathy with DOK7 mutation

  1. Motor-dominant chronic inflammatory demyelinating polyradiculoneuropathy with uhthoff-like phenomenon is a distinct clinical entity?

    Muscle & Nerve

    Volume 46, Issue 1, July 2012, Pages: 140–142, Masaki Kobayashi, Takanori Yokota, Hiroyuki Tomimitsu, Satoru Ishibshi, Teruhiko Sekiguchi, Tadasi Kanouchi, Kinya Ishikawa and Hidehiro Mizusawa

    Version of Record online : 12 JUN 2012, DOI: 10.1002/mus.23308

  2. You have free access to this content
    Goserelin Cannot Improve the Weakness of a Patient with Kennedy Disease after 40-Week Administration

    CNS Neuroscience & Therapeutics

    Volume 18, Issue 12, December 2012, Pages: 1021–1023, Zhi-Guang Shi, De-Ke Jiang, Mei Zhao and She-Qing Zhang

    Version of Record online : 2 NOV 2012, DOI: 10.1111/cns.12022

  3. Relapsing polyradiculoneuropathy as a neurological manifestation of systemic lupus erythematosus

    Muscle & Nerve

    Volume 46, Issue 5, November 2012, Pages: 828–829, Yuebing Li and Krista Remmel

    Version of Record online : 10 OCT 2012, DOI: 10.1002/mus.23439

  4. Sonographic features in hereditary neuropathy with liability to pressure palsies

    Muscle & Nerve

    Volume 45, Issue 6, June 2012, Pages: 920–921, Marta Lucchetta, Chiara Dalla Torre, Giuseppe Granata, Chiara Briani and Luca Padua

    Version of Record online : 10 MAY 2012, DOI: 10.1002/mus.23363

  5. Coexistence of CMT1A and diabetes mellitus in a young woman with a severe and progressive neuropathy and respiratory insufficiency

    Muscle & Nerve

    Volume 47, Issue 1, January 2013, Pages: 141–142, Monica A. Carvalho, Juliana B. Secchin, Charles M. Lourenço, Rita C.C. Leal, Keity C. Bueno, Amilton A. Barreira and Wilson Marques Jr.

    Version of Record online : 27 SEP 2012, DOI: 10.1002/mus.23459

  6. Rituximab therapy for morvan syndrome associated with myasthenia gravis

    Muscle & Nerve

    Volume 46, Issue 1, July 2012, Pages: 139–140, Michael Weiss

    Version of Record online : 12 JUN 2012, DOI: 10.1002/mus.23311

  7. Pharyngeal-cervical-brachial variant of Guillain–Barre syndrome with predominant bulbar palsy as the initial presentation of systemic lupus erythematosus and lupus nephritis: a case report

    International Journal of Rheumatic Diseases

    Volume 15, Issue 6, December 2012, Pages: e162–e164, Anjali Rajadhyaksha and Sonal Mehra

    Version of Record online : 8 JUL 2012, DOI: 10.1111/j.1756-185X.2012.01761.x

  8. Clinicopathological features of the first Asian family having vocal cord and pharyngeal weakness with distal myopathy due to a MATR3 mutation

    Neuropathology and Applied Neurobiology

    Volume 41, Issue 3, April 2015, Pages: 391–398, Satoshi Yamashita, Akira Mori, Yasuto Nishida, Ryoichi Kurisaki, Nozomu Tawara, Tomo Nishikami, Yohei Misumi, Hidetsugu Ueyama, Shigehiro Imamura, Yujiro Higuchi, Akihiro Hashiguchi, Itsuro Higuchi, Shinichi Morishita, Jun Yoshimura, Makoto Uchino, Hiroshi Takashima, Shoji Tsuji and Yukio Ando

    Version of Record online : 4 MAR 2015, DOI: 10.1111/nan.12179

  9. Cranial, axial and proximal myopathy and hypertrophic cardiomyopathy caused by a mutation in the globular head region of the MYH7 gene

    European Journal of Neurology

    Volume 21, Issue 6, June 2014, Pages: e51–e52, J. Díaz-Manera, A. Alejaldre, J. Llauger, S. Mirabet, R. Rojas-García, A. Ramos-Fransi, E. Gallardo and I. Illa

    Version of Record online : 8 MAY 2014, DOI: 10.1111/ene.12416

  10. Longstanding right-hand weakness in a patient with myasthenia gravis

    Muscle & Nerve

    Volume 34, Issue 5, November 2006, Pages: 670–671, Mamede de Carvalho and Ruth Geraldes

    Version of Record online : 28 JUL 2006, DOI: 10.1002/mus.20617

  11. Rapid worsening of IgM anti-MAG demyelinating polyneuropathy during rituximab treatment

    Journal of the Peripheral Nervous System

    Volume 18, Issue 2, June 2013, Pages: 189–191, Abraham C. J. Stork, Nicolette C. Notermans, Alexander F. J. E. Vrancken, David R. Cornblath and W-Ludo van der Pol

    Version of Record online : 19 JUN 2013, DOI: 10.1111/jns5.12018

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    A Case of Late-onset Riboflavin Responsive Multiple acyl-CoA Dehydrogenase Deficiency with Novel Mutations in ETFDH Gene

    CNS Neuroscience & Therapeutics

    Volume 18, Issue 11, November 2012, Pages: 952–954, Zhang-Ning Zhao, Meng-Xin Bao, Gao-Ting Ma, Xiao-Min Liu, Wen-Juan Xu, Zhong-Wen Sun, Huan Chen and Mei-Jia Zhu

    Version of Record online : 29 OCT 2012, DOI: 10.1111/cns.12007

  13. Diaphragmatic involvement without bulbar dysfunction or features to suggest amyotrophic lateral sclerosis in brachial amyotrophic diplegia

    Muscle & Nerve

    Volume 40, Issue 6, December 2009, Pages: 1066–1067, Ranjit Ramdass, Godwin U. Lekwuwa and Douglas Mitchell

    Version of Record online : 16 SEP 2009, DOI: 10.1002/mus.21435

  14. Potential predictors of response to immunomodulation in patients with myasthenia gravis

    Muscle & Nerve

    Volume 46, Issue 6, December 2012, Page: 982, Hai-Feng Li, Tao Liu, Yu Hong and Hong-Liang Zhang

    Version of Record online : 26 NOV 2012, DOI: 10.1002/mus.23495

  15. Relapsing–remitting severe generalized muscular weakness after botulinum toxin treatment for hyperhidrosis

    Muscle & Nerve

    Volume 50, Issue 3, September 2014, Pages: 456–457, Daniela Chiarello, Marianna Piombo, Marzia Corbetto, Giovanni Di Pino, Giovanni Assenza, Fioravante Capone and Vincenzo Di Lazzaro

    Version of Record online : 5 AUG 2014, DOI: 10.1002/mus.24304

  16. Dystonia with superimposed myasthenia gravis: An experiment in nature

    Movement Disorders

    Volume 23, Issue 11, 15 August 2008, Pages: 1626–1627, Archana Hinduja, Sudhanshu Chokroverty, Philip Hanna and Raji P. Grewal

    Version of Record online : 25 JUN 2008, DOI: 10.1002/mds.22166

  17. Phenotypic variability in a dystonia family with mutations in the manganese transporter gene

    Movement Disorders

    Volume 28, Issue 5, May 2013, Pages: 685–686, Cathérine C. S. Delnooz, Ron A. Wevers, Marialuisa Quadri, Peter T. Clayton, Philippa B. Mills, Karin Tuschl, Eric J. Steenbergen, Vincenzo Bonifati and Bart P. C. van de Warrenburg

    Version of Record online : 16 APR 2013, DOI: 10.1002/mds.25390

  18. Myasthenia gravis exacerbation after cetirizine administration

    Muscle & Nerve

    Volume 44, Issue 1, July 2011, Pages: 146–147, Alvaro Cobo Calvo, Maria Antònia Albertí Aguiló and Carlos Casasnovas Pons

    Version of Record online : 14 JUN 2011, DOI: 10.1002/mus.22096

  19. Andersen-Tawil syndrome presenting as a fixed myopathy

    Muscle & Nerve

    Volume 48, Issue 4, October 2013, Page: 623, Nicholas D. Child, James C. Cleland and Richard Roxburgh

    Version of Record online : 30 AUG 2013, DOI: 10.1002/mus.23872

  20. A patient with mutation in the SCN4A p.M1592v presenting with fixed weakness, rhabdomyolysis, and episodic worsening of weakness

    Muscle & Nerve

    Volume 48, Issue 2, August 2013, Pages: 306–307, Eric Lee and Nizar Chahin

    Version of Record online : 26 JUN 2013, DOI: 10.1002/mus.23803