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Caring for children with spinal muscular atrophy in Greece: parents' and caregivers' experience with the healthcare system Frontiers

Repurposed Nrf2 activator dimethyl fumarate rescues muscle inflammation and fibrosis in an aggravated mdx mouse model of Duchenne muscular dystrophy ScienceDirect.com

TREAT-NMD, a Leading Global NeuroMuscular Diseases Registry Network, and Aetion Announce Partnership on Real-World Evidence PR Newswire

(PDF) Collagen type VI regulates TGF-β bioavailability in skeletal muscle in mice researchgate.net

A contemporary analysis of the Australian clinical and genetic landscape of spinal muscular atrophy: a registry based study The Lancet

Injectable borax-loaded alginate hydrogels reduce muscle atrophy, modulate inflammation, and promote neuroprotection in the SOD1G93A mouse model of ALS through mechanisms involving IGF–Akt–mTOR signaling ScienceDirect.com

Resolvin-D2 targets myogenic cells and improves muscle regeneration in Duchenne muscular dystrophy Nature

The Italian neuromuscular registry: a coordinated platform where patient organizations and clinicians collaborate for data collection and multiple usage Orphanet Journal of Rare Diseases

The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations Wiley Online Library

Care for Patients With Neuromuscular Disorders in the COVID-19 Pandemic Era Frontiers

Time to diagnosis of Duchenne muscular dystrophy in Austria and Germany | Scientific Reports Nature

Oral administration of plumbagin is beneficial in in vivo models of Duchenne muscular dystrophy through control of redox signaling ScienceDirect.com

European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERN EURO-NMD) Wiley Online Library

Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the mdx Mouse Model and Patients Frontiers

Cellular variability of nonsense-mediated mRNA decay Nature

Morpholino Oligomer-Induced Dystrophin Isoforms to Map the Functional Domains in the Dystrophin Protein ScienceDirect.com

Oxidative Stress, Inflammation, and Activators of Mitochondrial Biogenesis: Tempol Targets in the Diaphragm Muscle of Exercise Trained-mdx Mice Frontiers

Exosome-mediated improvement in membrane integrity and muscle function in dystrophic mice ScienceDirect.com

Voluntary wheel running improves molecular and functional deficits in a murine model of facioscapulohumeral muscular dystrophy ScienceDirect.com

A cell-penetrating peptide enhances delivery and efficacy of phosphorodiamidate morpholino oligomers in mdx mice ScienceDirect.com

The ClC-1 chloride channel inhibitor NMD670 improves skeletal muscle function in rat models and patients with myasthenia gravis Science | AAAS

Multilayered regulations of alternative splicing, NMD, and protein stability control temporal induction and tissue-specific expression of TRIM46 during axon formation Nature

A Family of Laminin α2 Chain-Deficient Mouse Mutants: Advancing the Research on LAMA2-CMD Frontiers

Molecular profiling of individual FDA-approved clinical drugs identifies modulators of nonsense-mediated mRNA decay ScienceDirect.com

Nonsense-mediated RNA decay and its bipolar function in cancer Molecular Cancer

Extracellular vesicles from adipose-derived stem cells promote microglia M2 polarization and neurological recovery in a mouse model of transient middle cerebral artery occlusion Stem Cell Research & Therapy

Metabolomes of mitochondrial diseases and inclusion body myositis patients: treatment targets and biomarkers EMBO Press

mRNAs containing NMD-competent premature termination codons are stabilized and translated under UPF1 depletion Nature

European research networks to facilitate drug research in children British Pharmacological Society | Journals