Disease: Normokalemic periodic paralysis
- A case of multifocal papillary carcinoma and thyrotoxicosis: Hypokalemic periodic paralysis
- A dangerous food binge: a case report of hypokalemic periodic paralysis and review of current literature
- A new clinical entity in T704M mutation in periodic paralysis
- 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 role for external Ca2+ in maintaining muscle contractility in periodic paralysis
- Anaesthesia challenges of a parturient with paramyotonia congenita and terminal filum lipoma presenting for labour and caesarean section under epidural anaesthesia - a case report
- Analysis of the genetic background associated with sporadic periodic paralysis in Japanese patients
- 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 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
- Childbirth with epidural analgesia in a pregnant woman with hypokalemic periodic paralysis
- Clinical and genetic analysis of a patient with Gitelman syndrome misdiagnosed as 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
- 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
- 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
- First-Onset Hypokalemic Periodic Paralysis Following Surgery for Myxopapillary Ependymoma
- Further evidence for shared genetic susceptibility in both sporadic and Thyrotoxic periodic paralysis
- 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 aggravated by voltage - gate sodium channel blocker antiepileptic drug?
- 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 as an initial presentation of Sjogren syndrome
- 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
- Improving genetic diagnostics of skeletal muscle channelopathies
- Long-term efficacy and safety of dichlorphenamide for treatment of primary periodic paralysis
- Lower Ca2+ enhances the K+-induced force depression in normal and HyperKPP mouse muscles
- 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
- Myotonia congenita and periodic hypokalemia paralysis in a consanguineous marriage pedigree: Coexistence of a novel CLCN1 mutation and an SCN4A mutation
- 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 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
- Permanent muscle weakness in hypokalemic periodic paralysis
- 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
- 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
- Tumors masquerading as neurological diseases: A caution for clinicians in planning diagnosis and treatment
- 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 Ca<sup>2+</sup> release is impaired in hypokalemic periodic paralysis caused by Ca<sub>V</sub>1.1-R528H but not by Na<sub>V</sub>1.4-R669H