Myopathies of Infancy and Childhood | Pediatric Annals
Approach to myopathy
Brody myopathy: MedlinePlus Genetics
Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling | Nature Genetics
Exome analysis identifies Brody myopathy in a family diagnosed with malignant hyperthermia susceptibility - Sambuughin - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Exome analysis identifies Brody myopathy in a family diagnosed with malignant hyperthermia susceptibility - Sambuughin - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Muscle Disorders | MedlinePlus
Muscle Toxicity of Drugs: When Drugs Turn Physiology into Pathophysiology | Physiological Reviews
Diversity of ATP2A1 mutations in patients with Brody disease. (A)... | Download Scientific Diagram
Brody syndrome: A clinically heterogeneous entity distinct from Brody disease: A review of literature and a cross-sectional clinical study in 17 patients - ScienceDirect
Phenotypic Spectrum of Myopathies with Recessive Anoctamin-5 Mutations - IOS Press
Western blot analysis of SERCA1 in Brody disease and control. All Brody... | Download Scientific Diagram
A Pattern Recognition Approach to Myopathy | Semantic Scholar
Ion Channel Disorders | Musculoskeletal Key
ziekte van Brody
Exome analysis identifies Brody myopathy in a family diagnosed with malignant hyperthermia susceptibility - Sambuughin - 2014 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Cells | Free Full-Text | Genetic Modifiers of Hereditary Neuromuscular Disorders and Cardiomyopathy
The clinical assessment and a guide to classification of the myopathies (Chapter 8) - Disorders of Voluntary Muscle
