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DuchenneMuscularDystrophy news

Daily Glucocorticoid Therapy Endorsed for Young Duchenne MD Patients


Muscular Dystrophy News - Jan 10, 2017
Long-term therapy with daily glucocorticoid therapy can improve clinical outcomes of young patients with Duchenne muscular dystrophy (DMD) without serious side effects, according to recent research. In “Long-Term Outcome of Interdisciplinary Management ...
 

Hospital and Researchers Awarded $2.2M for Duchenne Gene Therapy Investigation


Muscular Dystrophy News - Jan 9, 2017
“We would like to thank PPMD for funding this exciting trial for Duchenne muscular dystrophy,” Mendell and Rodino-Klapac wrote in a statement. “Based on our experience, we believe we have outlined a safe approach for delivery of a gene with the ...
 

Frontier Pharma | Duchenne Muscular Dystrophy & Becker Muscular Dystrophy | ResearchMoz


Medgadget (blog) - Jan 10, 2017
The Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD) pipeline consists of 84 molecules across all stages of development. GBI Research's analysis revealed a high degree of innovation and diversity in this indication, with 70% of ...
 

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Duchenne Muscular Dystrophy: Advances in Therapeutics by Chamberlain Hardcover B


 

NEW Duchenne Muscular Dystrophy by Alan Emery


 

Duchenne Muscular Dystrophy: Symptoms, Management & Prognosis by Samuel Alexandr


 

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Duchenne Muscular Dystrophy books

Neurobiology of Brain Disorders: Biological Basis of Neurological and Psychiatric Disorders


Neurobiology of Brain Disorders is the first book directed primarily at basic scientists to offer a comprehensive overview of neurological and neuropsychiatric disease. This book links basic, translational, and clinical research, covering the genetic, developmental, molecular, and cellular mechanisms underlying all major categories of brain disorders. It offers students, postdoctoral fellows, and researchers in the diverse fields of neuroscience, neurobiology, neurology, and psychiatry the tools they need to obtain a basic background in the major neurological and psychiatric diseases, and to discern connections between basic research and these relevant clinical conditions.
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Duchenne Muscular Dystrophy: Advances in Therapeutics


Duchenne Muscular Dystrophy (DMD) is one of the most prevalent genetic disorders of childhood and currently stands as an incurable condition. This authoritative guide provides a clear overview of the latest current and experimental approaches to the treatment of DMD and examines the clinical, genetic, and pathophysiological aspects of the disease in the context of emerging therapeutic modalities. The only available source on the subject, this reference emphasizes the importance of accurate diagnosis, carrier detection, and genetic counseling, and supplies state-of-the-art contributions on pharmacological interventions, regenerative medicine, and gene therapy.
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Precious Time: Children Living With Muscular Dystrophy


by: Thomas Bergman
Describes the life, including medical attention and various daily activities, of a nine-year-old boy with Duchenne muscular dystrophy.
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Dan & DMD: A Children's Book on Duchenne Muscular Dystrophy


by: Joseph Yasmeh
Dan's an up-beat boy who loves to have a blast. And like many young boys, he was born with Duchenne muscular dystrophy. This is his story.
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Duchenne Muscular Dystrophy


Duchenne Muscular Dystrophy Instructional Tutorial Video CanadaQBank.com.
 

BrainPOP animation about Duchenne Muscular Dystrophy


 

Duchenne Muscular Dystrophy by Dr Khalid Jamil Akhtar


By: http://www.ilmkidunya.com/ Duchenne muscular dystrophy (DMD) is a recessive X-linked form of muscular dystrophy, which results in muscle degeneration, ...
 

Tom's Story - Duchenne muscular dystrophy - Action Medical Research


http://www.action.org.uk/appeal/duchenne-muscular-dystrophy Tom has Duchenne muscular dystrophy, a rare and fatal condition that causes muscle weakness, ...
 

Duchenne Muscular Dystrophy and Dystrophin


Duchenne Muscular Dystrophy (DMD) is an genetic muscle-wasting disease that leads to disability and early death. In all cases of this disease, the gene for a ...