McArdle disease, also known as glycogen storage disease type V, is an inherited metabolic disorder marked by a deficiency of myophosphorylase, the enzyme essential for the breakdown of glycogen in ...
Dublin, Nov. 18, 2024 (GLOBE NEWSWIRE) -- The "Glycogen Storage Disorders (GSD): Competitive Landscape" report has been added to ResearchAndMarkets.com's offering. This reports provides a data-driven ...
Glycogen storage disorders are metabolic conditions that manifest in the first years of life. This inability to process and store glucose can be difficult to diagnose. Now, researchers who have ...
Unexplained left ventricular hypertrophy often prompts the diagnosis of hypertrophic cardiomyopathy, a sarcomere-protein gene disorder. Because mutations in the gene for AMP-activated protein kinase γ ...
DUBLIN--(BUSINESS WIRE)--The "Glycogen Storage Disorders (GSD) Ongoing Global Clinical Trials Analysis and Outlook" report has been added to ResearchAndMarkets.com's offering. Glycogen Storage ...
Glycogen Storage Disorders – Epidemiology Review – 2029 provides in depth understanding of historical and forecasted epidemiology of Glycogen Storage Disorders along with the trend analysis. The ...
Estimates suggest that glycogen storage diseases (GSD) affect from around one person in 40,000 to less than one person in 1,000,000, making them “ultra-rare” diseases. This results in diluted research ...
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