Nemaline myopathy

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Nemaline Myopathy What is nemaline myopathy? Nemaline myopathy (NM) is a group of rare, inherited conditions that affect muscle tone and strength. It is also

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Source URL: muscle.ca

- Date: 2013-11-30 21:29:35
    2

    Climb National Information Centre for Metabolic Diseases Nemaline Myopathy Other names that may be used for this disorder are: • Congenital Rod Disease • NM

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    Source URL: www.climb.org.uk

    - Date: 2016-06-15 10:38:48
      3Myopathy / Rare diseases / Nemaline myopathy / Congenital myopathy / Central core disease / Muscle biopsy / Neuromuscular disease / Malignant hyperthermia / X-linked myotubular myopathy / Health / Medicine / Centronuclear myopathy

      Journal http://jcn.sagepub.com/ of Child Neurology Consensus Statement on Standard of Care for Congenital Myopathies Ching H. Wang, James J. Dowling, Kathryn North, Mary K. Schroth, Thomas Sejersen, Frederic Shapiro, Jon

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      Source URL: www.ann.org.au

      Language: English - Date: 2012-04-05 00:23:08
      4Exercise physiology / Neurological disorders / Nemaline myopathy / Muscle / Weakness / Skeletal striated muscle / Myopathy / Anatomy / Biology / Muscular system

      AuPS News President Prof Graham Lamb La Trobe University [removed] National Secretary

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      Source URL: aups.org.au

      Language: English - Date: 2015-03-11 04:52:15
      5Limb-girdle muscular dystrophy / Duchenne muscular dystrophy / TREAT-NMD / Medical genetics / Neuromuscular disease / Neurology / Neuromuscular Disorders / Nemaline myopathy / Distal muscular dystrophy / Medicine / Health / Muscular dystrophy

      1 ANN Newsletter - No. 3 / May 2011 Official launch of the ANN The Rare Disease Symposium, held

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      Source URL: www.ann.org.au

      Language: English - Date: 2011-05-27 05:40:20
      6Genetic genealogy / Limb-girdle muscular dystrophy / Myotonic dystrophy / TREAT-NMD / Duchenne muscular dystrophy / Nemaline myopathy / Centronuclear myopathy / Myotonia / Facioscapulohumeral muscular dystrophy / Health / Muscular dystrophy / Medicine

      8-9 MARCHANN Workshop REPORT Executive

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      Source URL: www.ann.org.au

      Language: English - Date: 2012-05-07 00:31:02
      7Muscular system / Central core disease / Centronuclear myopathy / Congenital myopathy / Rare diseases / Myopathy / Nemaline myopathy / RYR1 / Muscle biopsy / Health / Anatomy / Medicine

      CHAPTER 15 Congenital myopathies Introduction The congenital myopathies are a clinically, genetically and pathologically heterogeneous group of muscle disorders defined by the presence of particular histopathological fea

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      Source URL: www.us.elsevierhealth.com

      Language: English
      8Centronuclear myopathy / Myopathy / Limb-girdle muscular dystrophy / Nemaline myopathy / Myotonic dystrophy / Weakness / Muscular Dystrophy Association / Health / Muscular dystrophy / Anatomy

      Muscular Dystrophy - and Much More Muscular Dystrophies Duchenne Becker Limb-Girdle Facioscapulohumeral

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      Source URL: osp.od.nih.gov

      Language: English - Date: 2014-01-13 09:19:53
      9Myopathy / Rare diseases / Nemaline myopathy / Congenital myopathy / Central core disease / Muscle biopsy / Neuromuscular disease / Malignant hyperthermia / X-linked myotubular myopathy / Health / Medicine / Centronuclear myopathy

      Journal http://jcn.sagepub.com/ of Child Neurology Consensus Statement on Standard of Care for Congenital Myopathies Ching H. Wang, James J. Dowling, Kathryn North, Mary K. Schroth, Thomas Sejersen, Frederic Shapiro, Jon

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      Source URL: www.curecmd.org

      Language: English - Date: 2012-12-17 15:48:19
      10Biology / Muscular system / Neurological disorders / Centronuclear myopathy / Myopathy / Congenital myopathy / FHL1 / Nemaline myopathy / Muscle biopsy / Health / Anatomy / Muscular dystrophy

      The University of Chicago Genetic Services Laboratories 5841 S. Maryland Ave., Rm. G701, MC 0077, Chicago, Illinois[removed]Toll Free: (888) UC GENES[removed]Local: ([removed]FAX: ([removed]

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      Source URL: www.curecmd.org

      Language: English - Date: 2013-09-26 19:23:00
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