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Muscular Dystrophy : A Concise Guide / edited by Raymond A. Huml.

Contributor(s): SpringerLink (Online service) | Huml, Raymond A., editor literario
Material type: materialTypeLabelE-bookPublisher: Cham, Switzerland : Springer, 2015Description: 1 recurso en línea (XXIV, 191 p.) : 43 ilustraciones, 30 ilustraciones en color.ISBN: 9783319173627.Subject: Farmacoterapia | Farmacoterapia | Salud pública | Salud pública | Medicina | Neurología | NeurologíaDDC classification: 616.8 Online resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)Digital Resources
Contents:
1. Introduction to Muscular Dystrophy -- 2.Muscular Dystrophy: Historical Background and Types -- 3.FSHD: The Most Common Type of MD? -- 4.Duchenne and Becker Muscular Dystrophies: Underlying Genetic and Molecular Mechanisms -- 5.An Overview of the Muscular Dystrophies: Underlying Genetic and Molecular Mechanisms -- 6.Transition from Childhood to Adult in Patients with Muscular Dystrophy -- 7.Overview of Current Treatments for Muscular Dystrophy -- 8.Physical Therapy and Orthotic Devices for Patients with Muscular Dystrophy -- 9.Orthopedic Care of Children with Muscular Dystrophy -- 10.Global Regulatory Landscape -- 11.Key Challenges to the Approval of Products to Treat Patients with Muscular Dystrophy -- 12.Pharmaceutical Products and Non-Pharmaceutical Interventions as Potential Treatments for Patients with Muscular Dystrophy -- 13.US Patient Advocacy Groups -- 14.Global and National Patient Registries -- 15.Summary -- Index.
Summary: This practical and concise guide offers an overview of muscular dystrophy's (MD) complicated features, treatment options and general resources.ÂYw treatments and a greater understanding of proteins and structures associated with MD are discussed along with long-term patient care.Â{u006C}so included are clinical and developmental challenges within the current regulatory landscape and recent scientific and clinical advances.Â4scular Dystrophy: A Concise Guide offers clinicians, researchers, pharmaceutical executives and patient advocacy groups an easy-to-read reference that provides the necessary perspectives of the care giver and patient.
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Holdings
Item type Current library Collection Call number Copy number Status Date due Barcode Item holds
LIBRO-E NO PRÉSTAMO LIBRO-E NO PRÉSTAMO Madrid Digital Acceso Electrónico (UEM) Ciencias de la Salud RC935.M7 M873 2015 EB (Browse shelf(Opens below)) .i11577903 Acceso electrónico eBOOK .i11577903
Total holds: 0

1. Introduction to Muscular Dystrophy -- 2.Muscular Dystrophy: Historical Background and Types -- 3.FSHD: The Most Common Type of MD? -- 4.Duchenne and Becker Muscular Dystrophies: Underlying Genetic and Molecular Mechanisms -- 5.An Overview of the Muscular Dystrophies: Underlying Genetic and Molecular Mechanisms -- 6.Transition from Childhood to Adult in Patients with Muscular Dystrophy -- 7.Overview of Current Treatments for Muscular Dystrophy -- 8.Physical Therapy and Orthotic Devices for Patients with Muscular Dystrophy -- 9.Orthopedic Care of Children with Muscular Dystrophy -- 10.Global Regulatory Landscape -- 11.Key Challenges to the Approval of Products to Treat Patients with Muscular Dystrophy -- 12.Pharmaceutical Products and Non-Pharmaceutical Interventions as Potential Treatments for Patients with Muscular Dystrophy -- 13.US Patient Advocacy Groups -- 14.Global and National Patient Registries -- 15.Summary -- Index.

This practical and concise guide offers an overview of muscular dystrophy's (MD) complicated features, treatment options and general resources.ÂYw treatments and a greater understanding of proteins and structures associated with MD are discussed along with long-term patient care.Â{u006C}so included are clinical and developmental challenges within the current regulatory landscape and recent scientific and clinical advances.Â4scular Dystrophy: A Concise Guide offers clinicians, researchers, pharmaceutical executives and patient advocacy groups an easy-to-read reference that provides the necessary perspectives of the care giver and patient.

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