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Neuromuscular Disorders, ISSN 0960-8966, 07/2019, Volume 29, Issue 7, pp. 543 - 548
Anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase myopathy is less common in children but has been associated with more favorable prognosis than adult... 
Immune mediated necrotizing myopathy | IMNM | HMGCR | Reducing body myopathy | 3-hydroxy-3-methylglutaryl-coenzyme A reductase | FHL1 | Viral antibodies | Enzymes | Thiols | Creatine kinase | Immunotherapy | Antibodies | Creatine | Index Medicus
Journal Article
Muscle & Nerve, ISSN 0148-639X, 01/2013, Volume 47, Issue 1, pp. 127 - 134
Journal Article
Journal Article
Journal of Neuropathology & Experimental Neurology, ISSN 0022-3069, 09/2013, Volume 72, Issue 9, pp. 833 - 845
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 10/2017, Volume 27, Issue 10, pp. 962 - 963
* We identified a novel mutation in FHL1 gene. * Muscle biopsy showed a reducing body myopathy. * Marked gluteus maximus hypertrophy was noted on MRI. 
Magnetic resonance imaging | Reducing body myopathy | FHL1 | NEUROSCIENCES | CLINICAL NEUROLOGY | Diagnosis | Hypertrophy | Neurosciences | Diagnostic imaging | Medical genetics | Index Medicus
Journal Article
Neuropediatrics, ISSN 0174-304X, 02/2010, Volume 41, Issue 1, pp. 43 - 46
Abstract OBJECTIVE: Reducing body myopathy (RBM) is a rare progressive disorder of muscle characterized by intracytoplasmic inclusions, which stain strongly... 
Short Communication | LIM | X-linked myopathy | reducing body myopathy | aggresomes | FHL1 | GENE | PEDIATRICS | ISOFORM | BINDING PROTEIN | CLINICAL NEUROLOGY
Journal Article
Muscle & Nerve, ISSN 0148-639X, 03/2007, Volume 35, Issue 3, pp. 322 - 326
Reducing‐body myopathy (RBM) is a rare myopathy characterized by the presence of unique sarcoplasmic inclusions called reducing bodies (RBs). We characterized... 
unfolded protein response | endoplasmic reticulum stress‐associated degradation (EDRA) | aggresome | endoplasmic reticulum stress | reducing‐body myopathy | Aggresome | Endoplasmic reticulum stress-associated degradation (EDRA) | Endoplasmic reticulum stress | Reducing-body myopathy | Unfolded protein response | reducing-body myopathy | endoplasmic reticulum stress-associated degradation (EDRA) | BODIES | CONGENITAL MYOPATHY | NEUROSCIENCES | Molecular Chaperones - metabolism | Humans | Valosin Containing Protein | Genetic Diseases, Inborn - genetics | Ubiquitin - metabolism | Endoplasmic Reticulum - metabolism | Male | Muscle, Skeletal - metabolism | Genetic Diseases, Inborn - pathology | RNA, Messenger - metabolism | Endoplasmic Reticulum - pathology | Heat-Shock Proteins - genetics | Tubulin - metabolism | Muscle Proteins - metabolism | Cell Cycle Proteins - genetics | Adult | Female | Genetic Diseases, Inborn - metabolism | Membrane Proteins - metabolism | Inclusion Bodies - metabolism | Child | Biomarkers - metabolism | Endoplasmic Reticulum - genetics | Membrane Proteins - genetics | Muscular Diseases - metabolism | Heat-Shock Proteins - metabolism | Biomarkers - analysis | Molecular Chaperones - genetics | Muscular Diseases - pathology | Rare Diseases | Protein Folding | Muscle Proteins - genetics | Inclusion Bodies - genetics | Muscle, Skeletal - physiopathology | Inclusion Bodies - pathology | Adenosine Triphosphatases - genetics | Muscle, Skeletal - pathology | Muscular Diseases - genetics | Index Medicus
Journal Article
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 01/2014, Volume 23, Issue 1, pp. 209 - 225
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 12/2008, Volume 183, Issue 6, pp. 1033 - 1048
Journal Article
Journal Article
Journal Article