Pages that link to "Q622828"
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The following pages link to hypokalemic periodic paralysis (Q622828):
Displaying 50 items.
- dichlorphenamide (Q3706987) (← links)
- SCN4A (Q14905707) (← links)
- CACNA1S (Q17854816) (← links)
- Practical aspects in the management of hypokalemic periodic paralysis (Q21245474) (← links)
- Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H (Q22008539) (← links)
- Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis (Q24295040) (← links)
- Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families (Q24673082) (← links)
- A mutation in the KCNE3 potassium channel gene is associated with susceptibility to thyrotoxic hypokalemic periodic paralysis (Q28213064) (← links)
- A calcium channel mutation causing hypokalemic periodic paralysis (Q28242375) (← links)
- Dihydropyridine receptor mutations cause hypokalemic periodic paralysis (Q28243593) (← links)
- Hypokalemic periodic paralysis: In vitro investigation of muscle fiber membrane parameters (Q28265960) (← links)
- Reduced expression and abnormal localization of the K(ATP) channel subunit SUR2A in patients with familial hypokalemic periodic paralysis (Q28266632) (← links)
- The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis (Q29398134) (← links)
- Atypical arrhythmic complications in familial hypokalemic periodic paralysis (Q33157733) (← links)
- Generalized epilepsy in a patient with hypokalemic periodic paralysis and cardiac arrhythmia. (Q33172992) (← links)
- A Korean family of hypokalemic periodic paralysis with mutation in a voltage-gated calcium channel (R1239G) (Q33599318) (← links)
- Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis (Q33763782) (← links)
- Fatal dysrhythmia following potassium replacement for hypokalemic periodic paralysis (Q33774281) (← links)
- Thyrotoxic hypokalemic periodic paralysis case report and review of the literature (Q33919638) (← links)
- Disrupted coupling of gating charge displacement to Na+ current activation for DIIS4 mutations in hypokalemic periodic paralysis (Q33964031) (← links)
- Skeletal muscle sodium current is reduced in hypokalemic periodic paralysis (Q34011949) (← links)
- Ion permeation and block of the gating pore in the voltage sensor of NaV1.4 channels with hypokalemic periodic paralysis mutations (Q34028248) (← links)
- Extracellular potassium homeostasis: insights from hypokalemic periodic paralysis (Q34039490) (← links)
- Hypokalemic periodic paralysis: a case series, review of the literature and update of management (Q34101961) (← links)
- Hypokalemic periodic paralysis: two case reports. (Q34164314) (← links)
- Thyrotoxic periodic paralysis: an overview (Q34383789) (← links)
- An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel geneSCN4A (Q34417442) (← links)
- Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family (Q35054061) (← links)
- Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current (Q35208537) (← links)
- Idiopathic generalized epilepsy and hypokalemic periodic paralysis in a family of South Indian descent (Q35373045) (← links)
- Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype (Q35606217) (← links)
- Hypokalemic periodic paralysis; two different genes responsible for similar clinical manifestations. (Q35663783) (← links)
- Surgical treatment for thyrotoxic hypokalemic periodic paralysis: case report (Q35744982) (← links)
- A 20-year-old Chinese man with recurrent hypokalemic periodic paralysis and delayed diagnosis (Q35792289) (← links)
- Thyrotoxic hypokalemic periodic paralysis: six cases in non-Asian patients (Q35835463) (← links)
- Thyrotoxic hypokalemic periodic paralysis in a Native American patient: case report and literature review. (Q35839064) (← links)
- SCN4A-associated hypokalemic periodic paralysis merits a trial of acetazolamide (Q35959191) (← links)
- A primary Sjögren's syndrome patient with distal renal tubular acidosis, who presented with symptoms of hypokalemic periodic paralysis: Report of a case study and review of the literature (Q36029261) (← links)
- Comparative study of thyrotoxic periodic paralysis from idiopathic hypokalemic periodic paralysis: An experience from India (Q36180776) (← links)
- Thyrotoxic hypokalemic periodic paralysis in a Turkish male with graves' disease: a rare case report and review of the literature (Q36217294) (← links)
- A Na+ channel mutation linked to hypokalemic periodic paralysis exposes a proton-selective gating pore (Q36299707) (← links)
- A calcium channel mutant mouse model of hypokalemic periodic paralysis (Q36498120) (← links)
- Hypokalemic periodic paralysis as first sign of thyrotoxicosis (Q36760817) (← links)
- Hypokalemic periodic paralysis: a model for a clinical and research approach to a rare disorder (Q36774708) (← links)
- Hypokalemic Periodic Paralysis: a case report and review of the literature (Q36975334) (← links)
- Hypokalemic periodic paralysis as a manifestation of thyrotoxicosis. (Q37289962) (← links)
- Thyrotoxic hypokalemic periodic paralysis is a rare but potentially fatal emergency: case report and literature review. (Q37960063) (← links)
- Thyrotoxic hypokalemic periodic paralysis: two case reports and a brief review of literature (Q38155186) (← links)
- Cardiac arrhythmias in hypokalemic periodic paralysis: Hypokalemia as only cause? (Q38236485) (← links)
- Thyrotoxic, hypokalemic periodic paralysis (THPP) in adolescents (Q38242910) (← links)