The insulin-sensitivity sulphonylurea receptor variant is associated with thyrotoxic paralysis

A 10-year analysis of thyrotoxic periodic paralysis in 135 patients: focus on symptomatology and precipitants

(2013) Chin-Chun Chang et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis

(2012) Pei-Yi Chu et al.   CLINICA CHIMICA ACTA

A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis

(2012) Wallaya Jongjaroenprasert et al.   JOURNAL OF HUMAN GENETICS

Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3

(2012) Ching-Lung Cheung et al.   NATURE GENETICS

Ensembl 2013

(2012) Paul Flicek et al.   NUCLEIC ACIDS RESEARCH

Ion channelopathies in endocrinology: recent genetic findings and pathophysiological insights

(2011) Ana Luiza R. Rolim et al.   Arquivos Brasileiros de Endocrinologia e Metabologia

Novel etiopathophysiological aspects of thyrotoxic periodic paralysis

(2011) Rui M. B. Maciel et al.   Nature Reviews Endocrinology

The Ser1369Ala variant of ABCC8 and the risk for severe sulfonylurea-induced hypoglycemia in German patients with Type 2 diabetes

(2011) Judith Dina Holstein et al.   PHARMACOGENOMICS

Mutations in Potassium Channel Kir2.6 Cause Susceptibility to Thyrotoxic Hypokalemic Periodic Paralysis

(2010) Devon P. Ryan et al.   CELL

Type 2 Iodothyronine Deiodinase Levels Are Higher in Slow-Twitch than Fast-Twitch Mouse Skeletal Muscle and Are Increased in Hypothyroidism

(2010) Alessandro Marsili et al.   ENDOCRINOLOGY

SYMPOSIUM REVIEW: The role of the KATPchannel in glucose homeostasis in health and disease: more than meets the islet

(2010) James S. McTaggart et al.   JOURNAL OF PHYSIOLOGY-LONDON

ABCC8polymorphism (Ser1369Ala): influence on severe hypoglycemia due to sulfonylureas

(2010) Ryosuke Sato et al.   PHARMACOGENOMICS

Coexpression of the Type 2 Diabetes Susceptibility Gene Variants KCNJ11 E23K and ABCC8 S1369A Alter the ATP and Sulfonylurea Sensitivities of the ATP-Sensitive K+ Channel

(2009) K. S.C. Hamming et al.   DIABETES

Kir6.2 Variant E23K Increases ATP-Sensitive K+ Channel Activity and Is Associated With Impaired Insulin Release and Enhanced Insulin Sensitivity in Adults With Normal Glucose Tolerance

(2009) D. T. Villareal et al.   DIABETES

Genetic variations in the pancreatic ATP-sensitive potassium channel, β-cell dysfunction, and susceptibility to type 2 diabetes

(2008) D. A. Chistiakov et al.   ACTA DIABETOLOGICA

Insulin resistance in subjects with a history of thyrotoxic periodic paralysis (TPP)

(2008) Supamai Soonthornpun et al.   CLINICAL ENDOCRINOLOGY

Ser1369Ala Variant in Sulfonylurea Receptor Gene ABCC8 Is Associated With Antidiabetic Efficacy of Gliclazide in Chinese Type 2 Diabetic Patients

(2008) Y. Feng et al.   DIABETES CARE