Results 181 to 190 of about 44,988 (276)
ABSTRACT Background Low muscle oxidative capacity is an extrapulmonary manifestation of chronic obstructive pulmonary disease (COPD) with unclear aetiology. We sought to characterize locomotor muscle oxidative capacity in never smokers and ever smokers with and without COPD and determine clinical and behavioural features associated with low muscle ...
Alessandra Adami +5 more
wiley +1 more source
ABSTRACT Background Duchenne muscular dystrophy (DMD) is a severe, life‐limiting neuromuscular disorder (NMD) characterized by progressive muscle wasting and mitochondrial dysfunction. Although gene therapies offer promise, even those already approved by regulatory agencies, their use remains constrained by mutation specificity, delivery challenges and
Sean Y. Ng +12 more
wiley +1 more source
A case of mitochondrial myopathy and chronic progressive external ophthalmoplegia. [PDF]
Liu H +8 more
europepmc +1 more source
Anesthetic management of a case with adrenoleukodistrophy and mitochondrial myopathy [PDF]
Şennur Uzun, Zeynep Şener
openalex +1 more source
ABSTRACT Background Skeletal muscle wasting and weakness are prominent disease features. Originally considered to arise from common transcriptional changes, recent analyses demonstrated that different stimuli induce muscle wasting via largely distinct mRNA and protein changes.
Anna Stephan +6 more
wiley +1 more source
OMA1 mediates local and global stress responses against protein misfolding in CHCHD10 mitochondrial myopathy. [PDF]
Shammas MK +16 more
europepmc +1 more source
Sertraline‐Associated Riboflavin‐Responsive Lipid Storage Myopathy: Report of Two Case
Sertraline exposure can lead to an acquired riboflavin‐responsive multiple acyl‐CoA dehydrogenase deficiency (MADD). In patients with this acquired form of MADD, riboflavin supplementation can even lead to full clinical recovery and marked serological recovery before discontinuation of sertraline.
Aziz Shaibani, Alexis Taylor
wiley +1 more source
Serum GDF-15 Levels Accurately Differentiate Patients with Primary Mitochondrial Myopathy, Manifesting with Exercise Intolerance and Fatigue, from Patients with Chronic Fatigue Syndrome. [PDF]
Bermejo-Guerrero L +11 more
europepmc +1 more source
Mitochondrial Myopathy Studies on Permeabilized Muscle Fibers1 [PDF]
Thierry Letellier +5 more
openalex +1 more source
This work proposes ferroptosis as a mechanistic driver of age‐related muscle dysfunction, whereby iron dyshomeostasis and impaired antioxidant capacity promote lipid peroxidation, and eventually trigger ferroptosis, leading to muscle wasting, and ultimately contributing to weakness and functional decline with aging.
Rola S. Zeidan +6 more
wiley +1 more source

