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Publications by Scott Grist
Leigh Syndrome Caused by the MT-ND5 M.13513G>A Mutation: A Case Presenting With WPW-Like Conduction Defect, Cardiomyopathy, Hypertension and Hyponatraemia
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Related publications
A Mutation in MT-TW Causes a tRNA Processing Defect and Reduced Mitochondrial Function in a Family With Leigh Syndrome
Mitochondrion
Molecular Medicine
Cell Biology
Molecular Biology
A Case Concealed WPW Syndrome With Enhanced A-H Conduction
Japanese Journal of Electrocardiology
Illness-Induced Exacerbation of Leigh Syndrome in a Patient With the MTATP6 Mutation, M. 9185 T>C
Mitochondrion
Molecular Medicine
Cell Biology
Molecular Biology
Septal Myectomy for Severe Neonatal Hypertrophic Cardiomyopathy Caused by PTPN11 Gene Mutation: A Case Report
Biomedical Journal of Scientific & Technical Research
Primary Electrical Disorder or Primary Cardiomyopathy?: A Case With a Unique Association of Noncompaction Cardiomyopathy and Cathecolaminergic Polymorphic Ventricular Tachycardia Caused by Ryanodine Receptor Mutation
Circulation
Cardiovascular Medicine
Physiology
Cardiology
A Case With Infectious Mononucleosis-Like Syndrome Caused by Human Herpes Virus-6 Infection
Kansenshogaku zasshi. The Journal of the Japanese Association for Infectious Diseases
Medicine
The Wolff-Parkinson-White (WPW) Syndrome With Supernormal Conduction Through the Anomalous Bypass
Circulation
Cardiovascular Medicine
Physiology
Cardiology
A Serine Synthesis Defect Presenting With a Charcot-Marie-Tooth–Like Polyneuropathy
Archives of Neurology
Familial Dilated Cardiomyopathy Caused by an Alpha-Tropomyosin Mutation
Journal of the American College of Cardiology
Cardiovascular Medicine
Cardiology
