Cardiac conduction myotonic dystrophy. Medical search. Frequent questions

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Anatomy17

Heart Conduction System Atrioventricular Node Myocytes, Cardiac Bundle of His Purkinje Fibers Heart Myocardium Sinoatrial Node Muscle, Skeletal Heart Ventricles Chromosomes, Human, Pair 19 Heart Atria Gap Junctions Myoblasts Muscles Chromosomes, Human, 19-20 Muscle Fibers, Skeletal

Organisms4

Mice, Transgenic Dogs Mice, Inbred mdx Mice, Knockout

Diseases30

Myotonic Dystrophy Muscular Dystrophies Myotonic Disorders Arrhythmias, Cardiac Heart Block Muscular Dystrophy, Duchenne Corneal Dystrophies, Hereditary Muscular Dystrophy, Animal Myotonia Sinus Arrest, Cardiac Muscular Dystrophy, Facioscapulohumeral Atrioventricular Block Muscular Dystrophy, Emery-Dreifuss Death, Sudden, Cardiac Brugada Syndrome Fuchs' Endothelial Dystrophy Kearns-Sayre Syndrome Bradycardia Retinal Dystrophies Heart Diseases Bundle-Branch Block Disease Models, Animal Cardiomyopathy, Dilated Myotonia Congenita Lens Diseases Long QT Syndrome Neuromuscular Diseases Neuroaxonal Dystrophies Syndrome Muscle Weakness

Chemicals and Drugs16

NAV1.5 Voltage-Gated Sodium Channel Connexins Sodium Channels Connexin 43 RNA-Binding Proteins Protein-Serine-Threonine Kinases Sp4 Transcription Factor Dystrophin Anti-Arrhythmia Agents Muscle Proteins T-Box Domain Proteins Lamin Type A RNA, Messenger RNA Homeodomain Proteins Sarcoglycans

Analytical, Diagnostic and Therapeutic Techniques and Equipment12

Electrocardiography Pedigree Cardiac Pacing, Artificial Electrophysiologic Techniques, Cardiac Models, Cardiovascular Pacemaker, Artificial Cardiac Output Disease Models, Animal Heart Rate DNA Mutational Analysis Cardiac Surgical Procedures Electromyography

Psychiatry and Psychology1

Bone Conduction

Phenomena and Processes19

Neural Conduction Trinucleotide Repeat Expansion Trinucleotide Repeats Mutation Action Potentials DNA Repeat Expansion Chromosomes, Human, Pair 19 Phenotype Cardiac Output Repetitive Sequences, Nucleic Acid Alternative Splicing Time Factors Heart Rate Base Sequence Gene Expression Regulation, Developmental Chromosomes, Human, 19-20 Lac Operon Exons Bone Conduction

Disciplines and Occupations2

Cardiac Electrophysiology Electrophysiology

Information Science2

Base Sequence Molecular Sequence Data

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Information Science

Myotonic Dystrophy Heart Conduction System Muscular Dystrophies Neural Conduction Myotonic Disorders Atrioventricular Node Arrhythmias, Cardiac NAV1.5 Voltage-Gated Sodium Channel Trinucleotide Repeat Expansion Heart Block Muscular Dystrophy, Duchenne Electrocardiography Myocytes, Cardiac Cardiac Electrophysiology Trinucleotide Repeats Corneal Dystrophies, Hereditary Bundle of His Purkinje Fibers Heart Muscular Dystrophy, Animal Myotonia Connexins Sodium Channels Sinus Arrest, Cardiac Myocardium Muscular Dystrophy, Facioscapulohumeral Atrioventricular Block Pedigree Muscular Dystrophy, Emery-Dreifuss Death, Sudden, Cardiac Connexin 43 Sinoatrial Node Brugada Syndrome Fuchs' Endothelial Dystrophy Mutation RNA-Binding Proteins Kearns-Sayre Syndrome Muscle, Skeletal Heart Ventricles Bradycardia Protein-Serine-Threonine Kinases Cardiac Pacing, Artificial Action Potentials Electrophysiologic Techniques, Cardiac Models, Cardiovascular DNA Repeat Expansion Retinal Dystrophies Heart Diseases Sp4 Transcription Factor Chromosomes, Human, Pair 19 Phenotype Mice, Transgenic Dystrophin Pacemaker, Artificial Bundle-Branch Block Heart Atria Cardiac Output Anti-Arrhythmia Agents Disease Models, Animal Gap Junctions Muscle Proteins Electrophysiology T-Box Domain Proteins Cardiomyopathy, Dilated Lamin Type A Repetitive Sequences, Nucleic Acid Alternative Splicing Myoblasts Time Factors Heart Rate Dogs DNA Mutational Analysis Muscles Myotonia Congenita RNA, Messenger Mice, Inbred mdx Cardiac Surgical Procedures Base Sequence Gene Expression Regulation, Developmental Lens Diseases Electromyography Chromosomes, Human, 19-20 Long QT Syndrome RNA Neuromuscular Diseases Molecular Sequence Data Homeodomain Proteins Neuroaxonal Dystrophies Sarcoglycans Mice, Knockout Syndrome Lac Operon Exons Muscle Weakness Muscle Fibers, Skeletal Bone Conduction

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