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Publications by Keshav K. Singh
Illness-Induced Exacerbation of Leigh Syndrome in a Patient With the MTATP6 Mutation, M. 9185 T>C
Mitochondrion
Molecular Medicine
Cell Biology
Molecular Biology
The Importance of Mitochondrial DNA in Aging and Cancer
Journal of Aging Research
Gerontology
Geriatrics
Related publications
Overlapping Leigh Syndrome/Myoclonic Epilepsy With Ragged Red Fibres in an Adolescent Patient With a Mitochondrial DNA A8344G Mutation
Frontiers in Neurology
Neurology
Phenotypic Variability of Leigh Syndrome Due to the ATP6/ATP8 Variant M.8561T>C
South Asian Research Journal of Applied Medical Sciences
Bifid T Waves Induced by Isoprenaline in a Patient With Brugada Syndrome
Heart
Cardiovascular Medicine
Cardiology
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
Pulmonary Embolism in a Patient With Factor v Leiden Mutation, Presenting With Symptoms of Asthma Exacerbation
Journal of Allergy and Clinical Immunology
Allergy
Immunology
Patient With iDEND Syndrome–Related Mutation
Diabetes Care
Internal Medicine
Endocrinology
Advanced
Metabolism
Specialized Nursing
Diabetes
De Novo Mutation of M.3243A>G Together With M.16093T>C Associated With Atypical Clinical Features in a Pedigree With MIDD Syndrome
Journal of Diabetes Research
Endocrinology
Metabolism
Diabetes
The Phenomenon of Reverse Mutation in a Patient With Wiskott–Aldrich Syndrome
Pediatric Hematology/Oncology and Immunopathology
Oncology
Pediatrics
Child Health
Allergy
Hematology
Perinatology
Immunology
Unexpected Exacerbation of Tracheal Stenosis in a Patient With Hunter Syndrome Undergoing Cardiac Surgery
Case Reports in Anesthesiology
