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Publications by Nils-göran Larsson
Progressive Increase of the Mutated Mitochondrial DNA Fraction in Kearns-Sayre Syndrome
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
Mitochondrial DNA, Diabetes and Pancreatic Pathology in Kearns-Sayre Syndrome
Diabetologia
Internal Medicine
Endocrinology
Metabolism
Diabetes
Classical Triad of Kearns-Sayre Syndrome
BMJ Case Reports
Medicine
Identical Large Scale Rearrangement of Mitochondrial DNA Causes Kearns-Sayre Syndrome in a Mother and Her Son
Journal of Medical Genetics
Genetics
Cochlear Implantation in a Patient With Mitochondrial Disease. Kearns-Sayre Syndrome. A Case Report.
Practica Otologica
Otorhinolaryngology
Mitochondrial DNA Deletion Diagnosed by Analysis of an Endomyocardial Biopsy Specimen From a Patient With Kearns-Sayre Syndrome and Complete Heart Block
Heart
Cardiovascular Medicine
Cardiology
Mitochondrial DNA-associated Leigh Syndrome
Anesthesia for a Patient With Kearns-Shy Syndrome.
THE JOURNAL OF JAPAN SOCIETY FOR CLINICAL ANESTHESIA
KIAA0586is Mutated in Joubert Syndrome
Human Mutation
Genetics
Reduced Glucose Sensation Can Increase the Fitness of Saccharomyces Cerevisiae Lacking Mitochondrial DNA
PLoS ONE
Multidisciplinary
