Related references
Note: Only part of the references are listed.Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reason
Felix Kleefeld et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2022)
Neutral Lipid Storage Diseases as Cellular Model to Study Lipid Droplet Function
Sara Missaglia et al.
CELLS (2019)
Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G > A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency
Hai-Zhu Chen et al.
CHINESE MEDICAL JOURNAL (2019)
Adolescent Hyperuricemia with Lipid Storage Myopathy: A Clinical Study
Jingzhe Han et al.
MEDICAL SCIENCE MONITOR (2019)
Metabolic lipid muscle disorders: biomarkers and treatment
Corrado Angelini et al.
THERAPEUTIC ADVANCES IN NEUROLOGICAL DISORDERS (2019)
Muscle Magnetic Resonance Imaging for the Differentiation of Multiple Acyl-CoA Dehydrogenase Deficiency and Immune-mediated Necrotizing Myopathy
Ya-Wen Zhao et al.
CHINESE MEDICAL JOURNAL (2018)
Lipid storage myopathies: Current treatments and future directions
Emily R. Vasiljevski et al.
PROGRESS IN LIPID RESEARCH (2018)
A Historical Cohort Study on the Efficacy of Glucocorticoids and Riboflavin Among Patients with Late-onset Multiple Acyl-CoA Dehydrogenase Deficiency
Xin-Yi Liu et al.
CHINESE MEDICAL JOURNAL (2016)
Riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency in 13 cases, and a literature review in mainland Chinese patients
Min Zhu et al.
JOURNAL OF HUMAN GENETICS (2014)
Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency
Jianying Xi et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2014)
Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency
Sarah C. Gruenert
ORPHANET JOURNAL OF RARE DISEASES (2014)
Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A
Zhi-Qiang Wang et al.
JOURNAL OF MOLECULAR MEDICINE-JMM (2011)
The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene
Klaus Gempel et al.
BRAIN (2007)