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Muscular dystrophy

  • This Letter Is for Families with Variant(S) in the Titin Gene, Also

    This Letter Is for Families with Variant(S) in the Titin Gene, Also

  • The Myotonic Dystrophies: Diagnosis and Management Chris Turner,1 David Hilton-Jones2

    The Myotonic Dystrophies: Diagnosis and Management Chris Turner,1 David Hilton-Jones2

  • Skeletal Muscle Channelopathies: a Guide to Diagnosis and Management

    Skeletal Muscle Channelopathies: a Guide to Diagnosis and Management

  • Evidence-Based Guideline: Evaluation, Diagnosis, and Management Of

    Evidence-Based Guideline: Evaluation, Diagnosis, and Management Of

  • Myopathies Infosheet

    Myopathies Infosheet

  • Clinical Approach to the Floppy Child

    Clinical Approach to the Floppy Child

  • Blueprint Genetics Comprehensive Muscular Dystrophy / Myopathy Panel

    Blueprint Genetics Comprehensive Muscular Dystrophy / Myopathy Panel

  • Duchenne and Becker Muscular Dystrophy

    Duchenne and Becker Muscular Dystrophy

  • AMERICAN ACADEMY of PEDIATRICS Cardiovascular

    AMERICAN ACADEMY of PEDIATRICS Cardiovascular

  • Muscular Dystrophies: What the Radiologist Should Know

    Muscular Dystrophies: What the Radiologist Should Know

  • Myotonic Dystrophy Type 2

    Myotonic Dystrophy Type 2

  • Epidemiological Study and Genetic Characterization of Inherited Muscle

    Epidemiological Study and Genetic Characterization of Inherited Muscle

  • The Neuromuscular Junction: Roles in Aging and Neuromuscular Disease

    The Neuromuscular Junction: Roles in Aging and Neuromuscular Disease

  • Patients with Genetically Confirmed IBMPFD Were Identified

    Patients with Genetically Confirmed IBMPFD Were Identified

  • Myotonic Dystrophy

    Myotonic Dystrophy

  • Cognitive Deficits in Myopathies

    Cognitive Deficits in Myopathies

  • Diagnosis of a Centronuclear Myopathy Case in Appalachia 20 Years from Symptom Onset Christopher Burrell BS1, Zachary Wilson DO2, Dominika Lozowska MD Bsc1

    Diagnosis of a Centronuclear Myopathy Case in Appalachia 20 Years from Symptom Onset Christopher Burrell BS1, Zachary Wilson DO2, Dominika Lozowska MD Bsc1

  • Duchenne and Becker Muscular Dystrophy) Policy Number: PG0411 ADVANTAGE | ELITE | HMO Last Review: 07/09/2019

    Duchenne and Becker Muscular Dystrophy) Policy Number: PG0411 ADVANTAGE | ELITE | HMO Last Review: 07/09/2019

Top View
  • Skeletal Muscle Channelopathies: Rare Disorders with Common Pediatric Symptoms
  • Muscular Dystrophy: a Public Health Challenge Muscular Dystrophy Public Health Need
  • PDF-Document
  • Muscular Dystrophy N
  • Muscular Dystrophy Interagency Collaboration
  • Facioscapulohumeral Muscular Dystrophy
  • A PDF of the Occupational Therapy Guidelines
  • Diagnosis and Management of Duchenne Muscular Dystrophy, Part 1
  • Facts About Myopathies Dear Friends: Hen I Was in My Early Teens, WI Was Having an Ice Cream at the Mall with Some Friends, and Suddenly I Couldn’T Move a Muscle
  • What Is Becker Muscular Dystrophy?
  • Differential Diagnosis of Myotonic Disorders
  • A Guide for Families Family Guide 1 // 64 2 // 64 Family Guide
  • Clinical and Pathological Study Ofa Case of Congenital Muscular Dystrophy
  • A Diagnostic Service for Rare Neuromuscular Disorders (All Ages)
  • Duchenne and Becker Muscular Dystrophy
  • Basic Information for Midwives
  • Diagnosis and Treatment of Limb-Girdle Muscular Dystrophy
  • Miyoshi Myopathy


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