• Order to parcel locker

    Order to parcel locker
  • easy pay

    easy pay
  • Reduced price
Muscular Dystrophy: Causes & Management

Muscular Dystrophy: Causes & Management

9781626184602
1,385.94 zł
1,247.34 zł Save 138.60 zł Tax included
Lowest price within 30 days before promotion: 1,247.34 zł
Quantity
Available in 4-6 weeks

  Delivery policy

Choose Paczkomat Inpost, Orlen Paczka, DPD or Poczta Polska. Click for more details

  Security policy

Pay with a quick bank transfer, payment card or cash on delivery. Click for more details

  Return policy

If you are a consumer, you can return the goods within 14 days. Click for more details

Description
Muscular Dystrophies include a heterogeneous series of diseases that range from childhood to adult onset cases, of difficult diagnosis and treatment. This book presents the state of the art in muscular dystrophies, after the molecular revolution. In the field of patients diagnosis, several advances have been done by recognising new entities. New techniques such as biochemical, molecular advancements, and the use of muscle MRI are collected that allow rapid diagnosis. Also, advances in therapy and therapeutical trials are presented in Duchenne and other muscular dystrophies and some novel treatments in glycogen storage disease by enzyme replacement are proposed. Both rehabilitation techniques and other treatments deserve particular attention for the improvements observed.
Product Details
74198
9781626184602
9781626184602

Data sheet

Publication date
2013
Issue number
1
Cover
hard cover
Pages count
482
Dimensions (mm)
180.00 x 260.00
Weight (g)
1070
  • Preface; Muscular Dystrophy:: The Present & the Future; History & Pathogenesis of Dystrophies; Biomarkers & Genetic Risk; Inflammation in Duchenne Muscular Dystrophy; MRI Involvement in Muscular Dystrophy; Clinical Scales for Evaluation of Muscular Dystrophies; Dystrophinopathies; Scapulo-peroneal Dystrophy; Facio Scapulo Humeral Muscular Dystrophy; Limb Girdle Muscular Dystrophies; Myotonic Dystrophy Type 1:: Clinical Features; DM2:: Clinical Features; Desminopathies; Myofibrillar Myopathies; Mitochondrial Myopathies & Ocular Myopathies; Dysferlinopathies; Anoctamine 5 Myopathies; Health Support:: Health Promotion For Family Having A Child with DMD; Psychosocial Stress & Coping Strategies of Parents with Duchenne Muscular Dystrophy Children during the Middle Stage; Rehabilitation in Muscular Dystrophy; Cardiac Problems in DMD; Ventilatory Assistance; GSDII & ERT; Drugs Interfering With Ubiquitin-Proteasome & Autophagy-Lysosome Systems To Treat Muscular Dystrophy; Muscle & Bone in Muscular Dystrophy:: Why Not?; Treatment with Steroids of DMD; The Emerging Biology of Muscle Stem Cells & their Therapy Strategies in Muscular Dystrophy; Index.
Comments (0)