• A case of multifocal papillary carcinoma and thyrotoxicosis: Hypokalemic periodic paralysis
• A case report of a MODY 10 family presenting as hypokalemic periodic paralysis
• A dangerous food binge: a case report of hypokalemic periodic paralysis and review of current literature
• A novel CACNA1S gene variant in a child with hypokalemic periodic paralysis: a case report and literature review
• A novel mutation of SCN4A gene causes hypokalemic periodic paralysis in a Chinese family
• A rare case of cephalexin-induced acute interstitial nephritis with hypokalemic periodic paralysis
• A single-center retrospective study on the clinical features of thyrotoxic periodic paralysis
• Acquired hyperkalaemia leading to periodic paralysis: an emergency department perspective
• Allele frequency of muscular genetic disorders in bull-catching (vaquejada) quarter horses
• Anaesthesia challenges of a parturient with paramyotonia congenita and terminal filum lipoma presenting for labour and caesarean section under epidural anaesthesia - a case report
• Anaesthetic management of a parturient with hypokalaemic periodic paralysis for caesarean section: A case report and review of the literature
• Andersen-Tawil syndrome presenting as premenstrual periodic paralysis
• Appeared inexplicable disorders of consciousness after general anesthesia tracheal tube drawing in endoscopic tympanoplasty
• Arterial blood gas analysis aids early differential diagnosis and treatment of primary and secondary hypokalaemic periodic paralysis
• Atypical Fracture of Femur in Association with Familial Hypokalemic Periodic Paralysis: A Case Report
• Atypical Normokalemic Case of Thyrotoxic Periodic Paralysis in a Pediatric Patient
• Atypical presentation of hypokalemic periodic paralysis: A case report
• Autophagy is affected in patients with hypokalemic periodic paralysis: an involvement in vacuolar myopathy?
• Case 13-2024: A 27-Year-Old Man with Leg Weakness
• Case report: Sodium and chloride muscle channelopathy coexistence: A complicated phenotype and a challenging diagnosis
• Case report: thyrotoxic periodic paralysis, an unusual cause of hypokalemia
• Childbirth with epidural analgesia in a pregnant woman with hypokalemic periodic paralysis
• Clinical and genetic spectrum of a Chinese cohort with SCN4A gene mutations
• Clinical features and recovery pattern of secondary hypokalaemic paralysis
• Co-existence of Congenital Adrenal Hyperplasia and Familial Hypokalemic Periodic Paralysis due to <em>CYP21A2</em> and <em>SCN4A</em> Pathogenic Variants
• Co-existence of Congenital Adrenal Hyperplasia and Familial Hypokalemic Periodic Paralysis due to CYP21A2 and SCN4A Pathogenic Variants
• Coincident Thyrotoxic Hypokalemic Periodic Paralysis and Cardiomyopathy
• Crossover randomized controlled trial of bumetanide to rescue an attack of exercise induced hand weakness in hypokalaemic periodic paralysis
• Diagnostics in skeletal muscle channelopathies
• Dichlorphenamide for Refractory Hyperkalemic Periodic Paralysis
• Distal renal tubular acidosis and hypokalaemic periodic paralysis during pregnancy
• Drug repurposing in skeletal muscle ion channelopathies
• Early-Onset Autosomal Dominant Myopathy with Vacuolated Fibers and Tubular Aggregates but No Periodic Paralysis, in a Patient with the c.1583G>A (p.R528H) mutation in the CACNA1S Gene
• Excitability properties of mouse and human skeletal muscle fibres compared by muscle velocity recovery cycles
• Familial periodic paralysis associated with a rare KCNJ5 variant that supposed to have incomplete penetrance
• Field Diagnosis and Treatment of Hypokalemic Periodic Paralysis by a Helicopter Emergency Medical Services Team
• Gating pore currents occur in CaV1.1 domain III mutants associated with HypoPP
• Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients
• Genetic Screening of Patients with Thyrotoxic Hypokalemic Periodic Paralysis: An Experience from a Tertiary Care Hospital in the Northeast of Brazil
• Genome-wide meta-analysis reveals novel susceptibility loci for thyrotoxic periodic paralysis
• Glucocorticoid-Induced Hypokalemic Periodic Paralysis after Short-Term Use of Tenofovir with Hypophosphatemia: A Case Report
• Hyperkalemic periodic paralysis associated with a novel missense variant located in the inner pore of Nav1.4
• Hyperkalemic periodic paralysis with paramyotonia and the anaesthetic implications
• Hypokalaemic periodic paralysis secondary to subclinical hyperthyroidism: an uncommon cause of acute muscle paralysis
• Hypokalemic paralysis due to renal tubular acidosis: uncommon initial manifestation of primary Sjögren´s syndrome
• Hypokalemic paralysis due to renal tubular acidosis: uncommon initial manifestation of primary Sjogrens syndrome
• Hypokalemic Periodic Paralysis Masquerading as a Compressive Neuraxial Lesion Following Lumbar Epidural Placement in a Parturient: A Case Report
• Hypokalemic periodic paralysis: a 3-year follow-up study
• Hypokalemic periodic paralysis: a systematic review of published case reports
• Identification of a <em>SCN4A</em> mutation in a large Chinese family with atypical normokalemic periodic paralysis using whole-exome sequencing
• Identification of a SCN4A mutation in a large Chinese family with atypical normokalemic periodic paralysis using whole-exome sequencing
• Long-term efficacy and safety of dichlorphenamide for treatment of primary periodic paralysis
• Morphological Alterations of the Sarcotubular System in Permanent Myopathy of Hereditary Hypokalemic Periodic Paralysis with a Mutation in the CACNA1S Gene
• Muscle Channelopathies
• Muscle channelopathies
• Muscle MRI in periodic paralysis shows myopathy is common and correlates with intramuscular fat accumulation
• Muscle weakness in the extremities in a man with Graves' disease
• Mutation spectrum and health status in skeletal muscle channelopathies in Japan
• Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete analysis of CACNA1S and SCN4A genes
• N-of-1 trial of salbutamol in hyperkalaemic periodic paralysis
• Next-generation sequencing application to investigate skeletal muscle channelopathies in a large cohort of Italian patients
• Novel <em>CACNA1S</em> mutation in hypokalaemic periodic paralysis
• Novel CACNA1S mutation in hypokalaemic periodic paralysis
• Optical measurement of gating pore currents in hypokalemic periodic paralysis model cells
• Pain as a significant symptom in patients with periodic paralysis-A cross-sectional survey
• Paroxysmal narrow complex tachycardia secondary to hypokalaemic periodic paralysis
• Periodic paralysis
• Periodic paralysis due to cumulative effects of rare variants in SCN4A with small functional alterations
• Peripheral nerve dysfunction in a patient with thyrotoxic periodic paralysis: Evidence from an axonal prolonged exercise test
• Potassium losing, aldosterone producing adrenocortical carcinoma: a rare presentation
• Prevalence and risk factors of low vitamin D levels in children and adolescents with familial hypokalemic periodic paralysis
• Prevalence of genetically confirmed skeletal muscle channelopathies in the era of next generation sequencing
• Primary Sjogren's syndrome presenting as hypokalaemic periodic paralysis and acute pancreatitis
• Quality of life in hypokalemic periodic paralysis - a survey
• Recurrent hypokalemic paralysis in hypothyroidism
• Refractory familial hypokalaemic periodic paralysis leading to cardiovascular compromise
• Renal tubular acidosis and nephrogenic diabetes insipidus caused by Sjogren's syndrome with hypokalemic periodic paralysis as the first symptom: A case report
• Retigabine suppresses loss of force in mouse models of hypokalaemic periodic paralysis
• Secondary hypokalemic periodic paralysis in Crohn disease: Two case reports
• Sinus arrest in familial hypokalemic periodic paralysis caused by SCN4A mutation: a case report
• Skeletal Muscle Channelopathies
• Skeletal muscle channelopathies: a guide to diagnosis and management
• Steroid-induced hypokalemic periodic paralysis: a case report and literature review
• Stroke-mimicking unilateral hypokalemic paralysis and literature review
• Targeted Therapies for Skeletal Muscle Ion Channelopathies: Systematic Review and Steps Towards Precision Medicine
• The clinical and genetic heterogeneity analysis of five families with primary periodic paralysis
• The long exercise test as a functional marker of periodic paralysis
• The role of nephrologists in management of hypokalemic periodic paralysis: a case report
• The Role of Nutrition and Physical Activity as Trigger Factors of Paralytic Attacks in Primary Periodic Paralysis
• Thyrotoxic hypokalemic periodic paralysis in two African black women
• Thyrotoxic periodic paralysis (TPP): assessment in the emergency department
• Thyrotoxic periodic paralysis associated with lactic metabolic acidosis: Case report of an African man and review of literature
• Thyrotoxic periodic paralysis in two sexagenarian men: A case report
• Thyrotoxic periodic paralysis presenting as a broad complex tachycardia
• Thyrotoxic periodic paralysis presenting with quadriparesis and hyperreflexia
• Thyrotropin-secreting pituitary adenomas presenting as hypokalemic periodic paralysis and abnormal elevation of androgen: a case report
• Tyreotoksisk periodisk paralyse
• Vacuoles, Often Containing Glycogen, Are a Consistent Finding in Hypokalemic Periodic Paralysis
• Voltage-dependent Ca(2+) release is impaired in hypokalemic periodic paralysis caused by Ca(V)1.1-R528H but not by Na(V)1.4-R669H
• Voltage-dependent Ca²⁺ release is impaired in hypokalemic periodic paralysis caused by Ca_V1.1-R528H but not by Na_V1.4-R669H