Myotonic dystrophy : disease mechanism, current management and therapeutic development /: disease mechanism, current management and therapeutic development. (2018)

• Record Type: Book
• Further Information: Note: Masanori P. Takahashi, Tsuyoshi Matsumura, editors.
• Editors: Takahashi, Masanori P; Matsumura, Tsuyoshi
• Contents: Genetics of myotonic dystrophy -- Molecular mechanisms of myotonic dystrophy : RNA-mediated pathogenesis and RNA-binding proteins -- Clinical features of skeletal muscle and their underlying molecular mechanism -- Cardiac involvements in myotonic dystrophy -- Clinical features of the central nervous system -- Brain pathology in myotonic dystrophy -- Molecular defects in the DM central nervous system -- Respiratory feature in myotonic dystrophy -- Glucose intolerance in myotonic dystrophy -- Lipid metabolism in myotonic dystrophy -- Dysphagia in myotonic dystrophy -- Diasease modeling and drug development with DM1 patient-derived iPS cells -- Therapeutic development in myotonic dystrophy.
• Publisher Details: Singapore : Springer
• Publication Date: 2018
• Extent: 1 online resource
• Subjects: 616.748; Myotonia atrophica; HEALTH & FITNESS -- Diseases -- General; MEDICAL -- Clinical Medicine; MEDICAL -- Diseases; MEDICAL -- Evidence-Based Medicine; MEDICAL -- Internal Medicine; Myotonia atrophica; Neurology; Cardiology; Metabolic Diseases; Human Genetics; Myotonic Dystrophy; Electronic books
• Languages: English
• ISBNs: 9789811305085; 9811305080; 9789811305092; 9811305099
• Related ISBNs: 9789811305078; 9811305072
• Notes: Note: Online resource; title from PDF file page (EBSCO, viewed November 6, 2018).
• Access Rights: Legal Deposit; Only available on premises controlled by the deposit library and to one user at any one time; The Legal Deposit Libraries (Non-Print Works) Regulations (UK).
• Access Usage: Restricted: Printing from this resource is governed by The Legal Deposit Libraries (Non-Print Works) Regulations (UK) and UK copyright law currently in force.