- Home
- » Tags
- » Channelopathy
Top View
- Ion Channel Pharmacology
- Genetic Neurological Channelopathies: Molecular Genetics and Clinical Phenotypes J Spillane,1,2 D M Kullmann,2,3 M G Hanna2,3
- Changes in Resurgent Sodium Current Contribute to the Hyperexcitability of Muscles in Patients with Paramyotonia Congenita
- Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic Advances
- Genetic Neurological Channelopathies: Molecular Genetics and Clinical Phenotypes J Spillane,1,2 D M Kullmann,2,3 M G Hanna2,3
- Stridor As a Neonatal Presentation of Skeletal Muscle Sodium Channelopathy
- Neurological Channelopathies T D Graves, M G Hanna
- Clinical and Molecular Data Define a Diagnosis of Arrhythmogenic Cardiomyopathy in a Carrier of a Brugada-Syndrome-Associated PK
- Link Between Pain and Olfaction in an Inherited Sodium Channelopathy
- Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: a Systematic Review of the Global Burden
- Lysosomal Storage Disease Upon Disruption of the Neuronal Chloride Transport Protein Clc-6
- Treatment Updates for Neuromuscular Channelopathies Nantaporn Jitpimolmard, MD1,2 Emma Matthews, MRCP, Phd1,3 Doreen Fialho, FRCP, Phd1,*
- Muscle Ion Channel Diseases
- Thyrotoxic Periodic Paralysis- a Case Report
- Sudden Cardiac Death and Inherited Channelopathy: Heart: First Published As 10.1136/Heartjnl-2011-300953 on 15 March 2012
- Connexin 26 Variant Carriers Have a Better Gastrointestinal Health: Is This the Heterozygote Advantage&Quest;
- Ion Channelopathies in Endocrinology
- Genetics and Cardiac Channelopathies
- Channelopathies That Lead to Sudden Cardiac Death: Clinical and Genetic Aspects
- Channelopathies: a Link Between Brain and Heart: the Model of Epilepsy
- Ion Channel Gene Mutations Causing Skeletal Muscle Disorders: Pathomechanisms and Opportunities for Therapy
- Therapy in Myotonic Disorders and in Muscle Channelopathies
- Structure-Based Assessment of Disease-Related Mutations in Human
- Prevalence and Incidence of Rare Diseases
- Paroxysmal Neuromyotonia: a New Sporadic Channelopathy
- Genetic Testing for Cardiac Channelopathies: Ten Questions Regarding Clinical Considerations for Heart Rhythm Allied Professionals
- Dr UMAR PHYSIOLOGY
- Hyperkalemic Periodic Paralysis: Case Report with a SCNA4 Gene Mutation and Literature Review
- Pain As a Channelopathy