• A novel RYR1 variant in an infant with a unique fetal presentation of central core disease
• Anesthetic management of a ventilator-dependent parturient with the King-Denborough syndrome
• Anesthetic management of the King-Denborough syndrome
• Dominantly inherited malignant hyperthermia (MH) in the King-Denborough syndrome
• Halothane-caffeine contracture testing in neuromuscular diseases
• Intraoperative Presentation of Malignant Hyperthermia (Confirmed by RYR1 Gene Mutation, c.7522C>T; p.R2508C) Leads to Diagnosis of King-Denborough Syndrome in a Child With Hypotonia and Dysmorphic Features: A Case Report
• Intraoperative Presentation of Malignant Hyperthermia (Confirmed by RYR1 Gene Mutation, c.7522C>T; p.R2508C) Leads to Diagnosis of King-Denborough Syndrome in a Child With Hypotonia and Dysmorphic Features: A Case Report
• King-denborough syndrome caused by a novel mutation in the ryanodine receptor gene
• King-Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene
• King-Denborough syndrome: contracture testing and literature review
• King-Denborough Syndrome: report of two Brazilian cases
• Malignant Hyperthermia
• Malignant hyperthermia and neuromuscular disease
• Pancreatitis in RYR1-related disorders
• Ryanodine receptor 1-related disorders: an historical perspective and proposal for a unified nomenclature
• Ryanodine Receptor 1-Related Myopathies: Diagnostic and Therapeutic Approaches
• RYR1-related congenital myopathy with fatigable weakness, responding to pyridostigimine