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Parent Project Muscular Dystrophy Company Profile

08:23 EDT 24th September 2017 | BioPortfolio


News Articles [702 Associated News Articles listed on BioPortfolio]

Parent Project Muscular Dystrophy Announces Duchenne Action Month this September

HACKENSACK, N.J., Sept. 1, 2017 /PRNewswire-USNewswire/ -- Parent Project Muscular Dystrophy (PPMD), a nonprofit organization leading the fight to end Duchenne muscular dystrophy (Duchenne), will...

Shortened telomeres linked to dysfunction in Duchenne muscular dystrophy, researchers find

A discovery about muscular dystrophy disorders has been made that suggests new possibilities for treatment. Researchers found that stem cells in the muscles of muscular dystrophy patients may, at an e...

Parent Project Muscular Dystrophy Announces Partnership with Perky Jerky®

HACKENSACK, N.J., Aug. 31, 2017 /PRNewswire-USNewswire/ -- Parent Project Muscular Dystrophy (PPMD), a nonprofit organization leading the fight to end Duchenne muscular dystrophy (Duchenne), is p...

Parent Project Muscular Dystrophy to Convene International Experts for Inflammation and Immunity in Duchenne Muscular Dystrophy Workshop

CHICAGO, June 28, 2017 /PRNewswire-USNewswire/ -- Parent Project Muscular Dystrophy (PPMD), a nonprofit organization leading the fight to end Duchenne muscular dystrophy (Duchenne), will convene ...

Parent Project Muscular Dystrophy to Fund $1 Million in Exon Skipping Projects

Leading Duchenne Organization Announces Request for Applications Focused on the Development of Oligos HACKENSACK, N.J., Aug. 14, 2013 /PRNewswire-USNewswire/ -- Parent Project Muscular Dystrop...

Researchers find shortened telomeres linked to dysfunction in Duchenne muscular dystrophy

Researchers from the Perelman School of Medicine at the University of Pennsylvania have made a discovery about muscular dystrophy disorders that suggest new possibilities for treatment. In a study pub...

Study: Drug Candidate Demonstrates Efficacy in Duchenne Muscular Dystrophy

NewsBiophytis clinical stage drug-candidate sarconeos demonstrates efficacy in preclinical models of Duchenne muscular dystrophy. Duchenne muscular dystrophy is a new 'Orphan' indication for Sarconeos...

Parent Project Muscular Dystrophy Grants $175,000 for Biomarkers, Non-Ambulatory Endpoints in Duchenne Muscular Dystrophy

Dr. Craig McDonald of UC Davis to Receive Supplemental Funds HACKENSACK, N.J., Jan. 18, 2013 /PRNewswire-USNewswire/ -- Parent Project Muscular Dystrophy (PPMD) has awarded Dr. Craig McDona...

PubMed Articles [1272 Associated PubMed Articles listed on BioPortfolio]

Translation and validation of the Life Satisfaction Index for Adolescents scale with neuromuscular disorders: LSI-A Brazil.

To validate the Life Satisfaction Index for Adolescents (LSI-A) scale, parent version and patient version, for Duchenne muscular dystrophy (DMD), spinal muscular atrophy (SMA) and limb-girdle muscular...

Parents' Reactions to the Diagnosis of Duchenne Muscular Dystrophy: Associations Between Resolution, Family Functioning, and Child Behavior Problems.

Duchenne muscular dystrophy (DMD) is the most frequent inherited form of muscular dystrophy during childhood. DMD is a severe and progressive disease. Children initially have no symptoms, but the diag...

Upper limb functional assessment scale for children with Duchenne muscular dystrophy and Spinal muscular atrophy.

Duchenne muscular dystrophy (DMD) and Spinal muscular atrophy (SMA) causes significant disability and progressive functional impairment. Readily available instruments that assess functionality, especi...

Longitudinal Community Walking Activity in Duchenne Muscular Dystrophy.

Natural history studies for Duchenne muscular dystrophy (DMD) have not included measures of community ambulation.

Energy expenditure, body composition, and prevalence of metabolic disorders in patients with Duchenne muscular dystrophy.

Duchenne muscular dystrophy (DMD) is a severe muscular disease characterized by progressive loss of functional muscle mass followed by changes in body composition.

Clinical Trials [2667 Associated Clinical Trials listed on BioPortfolio]

Ramipril Versus Carvedilol in Duchenne and Becker Patients

Data on preventive therapy in Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) affected individuals without cardiac involvement are very limited and currently lacking ...

Study of ACE-031 in Subjects With Duchenne Muscular Dystrophy

The purpose of this study is to determine if ACE-031 is safe and well-tolerated in children with Duchenne Muscular Dystrophy (DMD) and to select the optimal doses of ACE-031 in terms of sa...

A Study of TAS-205 for Duchenne Muscular Dystrophy

The objective of this study is to evaluate the efficacy after 24-week repeated oral doses of TAS-205 in patients with Duchenne Muscular Dystrophy (DMD) in an exploratory manner.

Cardiac Outcome Measures in Children With Muscular Dystrophy

The purpose of the research study is to evaluate different cardiac measures that are obtained by echocardiographic tests in patients with muscular dystrophy.

Biomechanical Analysis of Gait in Individuals With Duchenne Muscular Dystrophy

The purpose of this research study is to understand the walking patterns, strength and function changes of boys with Duchenne muscular dystrophy on/off corticosteroids to determine the bes...

Companies [1000 Associated Companies listed on BioPortfolio]

Parent Project Muscular Dystrophy

Biotechnology Industry Organization (BIO) and Parent Project Muscular Dystrophy (PPMD)

Tivorsan Pharmaceuticals, Inc.

Tivorsan Pharmaceuticals, Inc. is a protein therapeutics company pioneering a unique approach to treating serious neuromuscular disorders, including DMD and Becker Muscular...

The Muscular Dystrophy Association

Muscular Dystrophy Association

More Information about "Parent Project Muscular Dystrophy" on BioPortfolio

We have published hundreds of Parent Project Muscular Dystrophy news stories on BioPortfolio along with dozens of Parent Project Muscular Dystrophy Clinical Trials and PubMed Articles about Parent Project Muscular Dystrophy for you to read. In addition to the medical data, news and clinical trials, BioPortfolio also has a large collection of Parent Project Muscular Dystrophy Companies in our database. You can also find out about relevant Parent Project Muscular Dystrophy Drugs and Medications on this site too.

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