• A defective SERCA1 protein is responsible for congenital pseudomyotonia in Chianina cattle
• Abdominal closure in the critically ill patient
• Abnormal intracellular ca(2+)homeostasis and disease
• Absence of anti-HMG-CoA reductase autoantibodies in severe self-limited statin-related myopathy
• Advice from professional societies: appropriate use of NSAIDs
• Anesthetic Management of the Patient with Mitochondrial Disease: A Review of Current Best Evidence
• Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy
• Atypical nuclear abnormalities in a patient with Brody disease
• Autosomal dominant Brody disease cosegregates with a chromosomal (2;7)(p11.2;p12.1) translocation in an Italian family
• BAG3 (Bcl-2-Associated Athanogene-3) Coding Variant in Mice Determines Susceptibility to Ischemic Limb Muscle Myopathy by Directing Autophagy
• Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait: A Case Series of 9 Children
• Brody disease: insights into biochemical features of SERCA1 and identification of a novel mutation
• Brody disease: when myotonia is not myotonia
• Brody myopathy demonstrates a pseudo-increment on repetitive nerve stimulation
• Brody Myopathy Presenting as Recurrent Rhabdomyolysis
• Brody syndrome: a clinically heterogeneous entity distinct from Brody disease: a review of literature and a cross-sectional clinical study in 17 patients
• Brody syndrome: an underdiagnosed cause of muscle stiffness and cramps in children
• Ca2+ signalling and muscle disease
• Calcium Dynamics Mediated by the Endoplasmic/Sarcoplasmic Reticulum and Related Diseases
• Calcium ion in skeletal muscle: its crucial role for muscle function, plasticity, and disease
• Calcium regulation and muscle disease
• Case report: Clinical and molecular characterization of two siblings affected by Brody myopathy
• Case report: Revealing the rare-a Brody Disease patient from Turkey expanding the phenotype
• Cell-specific ablation of Hsp47 defines the collagen-producing cells in the injured heart
• Characterization of cDNA and genomic DNA encoding SERCA1, the Ca(2+)-ATPase of human fast-twitch skeletal muscle sarcoplasmic reticulum, and its elimination as a candidate gene for Brody disease
• Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy
• Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody disease
• Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients
• Continuous venovenous hemodiafiltration in hypernatremic hyperglycemic nonketotic coma
• Damage control in trauma and abdominal sepsis
• Detecting impaired muscle relaxation in myopathies with the use of motor cortical stimulation
• Development of a model-based clinical trial simulation platform to optimize the design of clinical trials for Duchenne muscular dystrophy
• Differential Analysis of Gly211Val and Gly286Val Mutations Affecting Sarco(endo)plasmic Reticulum Ca²⁺-ATPase (SERCA1) in Congenital Pseudomyotonia Romagnola Cattle
• Diminished force production and mitochondrial respiratory deficits are strain-dependent myopathies of subacute limb ischemia
• Disabilities and activities of daily living among veterans with old hip disarticulation and transpelvic amputation
• Disease causing mutations of troponin alter regulated actin state distributions
• Disturbed Ca²⁺ Homeostasis in Muscle-Wasting Disorders
• Efficacy and safety of an extended-release niacin (Niaspan): a long-term study
• Evidence of ER stress and UPR activation in patients with Brody disease and Brody syndrome
• Excitation-contraction-relaxation cycle: role of Ca2+-regulatory membrane proteins in normal, stimulated and pathological skeletal muscle (review)
• Excited delirium following use of synthetic cathinones (bath salts)
• Exome analysis identifies Brody myopathy in a family diagnosed with malignant hyperthermia susceptibility
• Exosome-Mediated miR-29 Transfer Reduces Muscle Atrophy and Kidney Fibrosis in Mice
• Expert consensus document: Mitochondrial function as a therapeutic target in heart failure
• Fast-twitch skeletal muscle fiber adaptation to SERCA1 deficiency in a Dutch Improved Red and White calf pseudomyotonia case
• Flat Anterior Chamber after Trabeculectomy in Secondary Angle-Closure Glaucoma with BEST1 Gene Mutation: Case Series
• GATM locus does not replicate in rhabdomyolysis study
• Genomewide Association Study of Statin-Induced Myopathy in Patients Recruited Using the UK Clinical Practice Research Datalink
• Gluteal compartment syndrome and sciatica after bone marrow biopsy: a case report and review of the literature
• Helping your patients with spasticity reach maximal function
• Humpty Dumpty on capsular contracture and complications
• Hypoxia Resistance Is an Inherent Phenotype of the Mouse Flexor Digitorum Brevis Skeletal Muscle
• Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease
• Identification of a pathogenic mutation in ATP2A1 via in silico analysis of exome data for cryptic aberrant splice sites
• Impaired contractile function of the supraspinatus in the acute period following a rotator cuff tear
• Induced in vivo knockdown of the Brca1 gene in skeletal muscle results in skeletal muscle weakness
• Inhibition of ubiquitin proteasome system rescues the defective sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA1) protein causing Chianina cattle pseudomyotonia
• Intracellular calcium: physiology and physiopathology
• Ion transport in human skeletal muscle cells: disturbances in myotonic dystrophy and Brody's disease
• Lambert-Brody syndrome
• Large-scale serum protein biomarker discovery in Duchenne muscular dystrophy
• Metabolic myopathies in adulthood. Features and clues for diagnosis
• Mitochondrial Regulation of the Muscle Microenvironment in Critical Limb Ischemia
• Mitochondrial therapy improves limb perfusion and myopathy following hindlimb ischemia
• MR imaging of the wrist and elbow
• Muscle cell derived angiopoietin-1 contributes to both myogenesis and angiogenesis in the ischemic environment
• Muscle function in a patient with Brody's disease
• Muscle MRI in patients with dysferlinopathy: pattern recognition and implications for clinical trials
• Muscle-Specific Ablation of Glucose Transporter 1 (GLUT1) Does Not Impair Basal or Overload-Stimulated Skeletal Muscle Glucose Uptake
• Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody disease
• Myopathy caused by a deficiency of Ca2+-adenosine triphosphatase in sarcoplasmic reticulum (Brody's disease)
• Nuclear Inositide Signaling Via Phospholipase C
• Overactive muscles: it can be more serious than common myalgia or cramp
• Palmaris Longus Tendinopathy Diagnosed With Ultrasound: A Case Report
• Paradoxical pseudomyotonia in English Springer and Cocker Spaniels
• Pathophysiological mechanisms leading to muscle loss in chronic kidney disease
• Permanent paralysis at sites of dermal exposure to chlorpyrifos
• PFKFB3-mediated glycolysis rescues myopathic outcomes in the ischemic limb
• Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing
• Predicting the severity of cocaine-associated rhabdomyolysis
• Predictive items of one-year mortality in nonagenarians. The NonaSantfeliu Study
• Pseudomyotonia, a muscle function disorder associated with an inherited ATP2A1 (SERCA1) defect in a Dutch Improved Red and White cross-breed calf
• Review of musculoskeletal injuries and prevention in the endoscopy practitioner
• SERCA pumps and human diseases
• SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers
• Spinal cord infarction with multiple etiologic factors
• Sports hernia repair with adductor tenotomy
• Structural study of skeletal muscle fibres in healthy and pseudomyotonia affected cattle
• Structure-function relationships in the Ca(2+)-binding and translocation domain of SERCA1: physiological correlates in Brody disease
• Structure/function analysis of the Ca2+ binding and translocation domain of SERCA1 and the role in Brody disease of the ATP2A1 gene encoding SERCA1
• Symptomatic pain and fibromyalgia treatment through multidisciplinary approach for primary care
• Targeted Expression of Catalase to Mitochondria Protects Against Ischemic Myopathy in High-Fat Diet-Fed Mice
• Temporal Association Between Ischemic Muscle Perfusion Recovery and the Restoration of Muscle Contractile Function After Hindlimb Ischemia
• The biomechanics of tennis elbow. An integrated approach
• The C-terminus of troponin T is essential for maintaining the inactive state of regulated actin
• The c.126C>A(p.(Cys42Ter)) SLC7A10 nonsense variant is a candidate causative variant for paradoxical pseudomyotonia in English Cocker and Springer Spaniels
• The mutation of Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA1) and is associated with Brody disease
• The role of ion-regulatory membrane proteins of excitation-contraction coupling and relaxation in inherited muscle diseases
• Thrombospondin expression in myofibers stabilizes muscle membranes
• Use of a picture archiving and communications system (PACS) and computed plain radiography in preoperative planning