• 2022 HRS expert consensus statement on evaluation and management of arrhythmic risk in neuromuscular disorders
• A Case Report of Kearns-Sayre Syndrome: Not an Absolute Contraindication for Radiotherapy
• A Patient With Kearns Sayre Syndrome and Charcot-Marie-Tooth for Supraventricular Tachycardia Ablation: A Case Report
• Adrenal Dysfunction in Mitochondrial Diseases
• Adrenal involvement in mitochondrial DNA deletion disorders is highly dependent on comorbidities and pituitary function
• Adrenal involvement in mtDNA deletion disorders is highly dependent on comorbidities and pituitary function
• Adrenocortical function in patients with Single Large Scale Mitochondrial DNA Deletions: a retrospective single centre cohort study
• Anesthetic Management in Double-Trouble Kearns-Sayre Syndrome and Hereditary Neuropathy Is Feasible but Delicate
• Anesthetic management of Kearns-Sayre syndrome. Case report
• Bilateral Ptosis and Ophthalmoplegia in a Young Man
• Case report: Clinical profile, molecular genetics, and neuroimaging findings presenting in a patient with Kearns-Sayre syndrome associated with inherited thrombophilia
• Case Report: Kearns Sayre Syndrome Complicated With Postpartum Cardiac Failure
• Cellular and Molecular Responses to Mitochondrial DNA Deletions in Kearns-Sayre Syndrome: Some Underlying Mechanisms
• Clinical and genetic analysis of a patient with HUPRA syndrome due to missense variants of SARS2 gene and literature review
• Clinical and molecular characterization of mitochondrial DNA disorders in a group of Argentinian pediatric patients
• Clinical Spectrum of Biopsy Proven Mitochondrial Myopathy
• Cochlear Implantation in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome: Case Presentation
• Correction to: Kearns-Sayre syndrome: expanding spectrum of a "novel" mitochondrial leukomyeloencephalopathy
• Correction to: Kearns‑Sayre syndrome: expanding spectrum of a "novel" mitochondrial leukomyeloencephalopathy
• Diabetes Out-of-the-Box: Diabetes Mellitus and Impairment in Hearing and Vision
• Diagnosing Kearns-Sayre syndrome requires clinical and genetic evidence
• Diagnosis of Kearns-Sayre syndrome requires genetic confirmation
• Diagnosis of Kearns-Sayre syndrome requires genetic confirmation
• Electrolyte Disorders in Mitochondrial Cytopathies: A Systematic Review
• Eye movement disorders in inborn errors of metabolism: A quantitative analysis of 37 patients
• Folic acid inhibits 5-methyltetrahydrofolate transport across the blood-cerebrospinal fluid barrier: Clinical biochemical data from two cases
• Generation and Evaluation of Isogenic iPSC as a Source of Cell Replacement Therapies in Patients with Kearns Sayre Syndrome
• Generation of human induced pluripotent stem cell (hiPSC) line UOMi005-A from PBMCs of a patient with Kearns-Sayre syndrome
• Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells: a comparison with Fanconi anemia
• Growth Retardation in the Course of Fanconi Syndrome Caused by the 4977-bp Mitochondrial DNA Deletion: A Case Report
• Have one's view of the important overshadowed by the trivial: chronic progressive external ophthalmoplegia combined with unilateral facial nerve injury: a case report and literature review
• High-grade idiopathic atrioventricular block in childhood: Case report and literature review
• Human induced pluripotent stem cell (hiPSC) line UOMi006-A derived from PBMCs of a patient with Kearns-Sayre syndrome
• Imaging Patterns Characterizing Mitochondrial Leukodystrophies
• Increased Sphingomyelin and Free Sialic Acid in Cerebrospinal Fluid of Kearns-Sayre Syndrome: New Findings Using Untargeted Metabolomics
• Involvement of the cardiac conduction system in Kearns-Sayre syndrome is progressive
• Involvement of the cardiac conduction system in Kearns-Sayre syndrome is progressive: Authors' reply
• Kearns Sayre syndrome: a rare etiology of complete atrioventricular block in children (case report)
• Kearns-Sayre Syndrome
• Kearns-Sayre Syndrome
• Kearns-Sayre syndrome case. Novel 5,9 kb mtDNA deletion
• KEARNS-SAYRE SYNDROME MASQUERADING AS MYASTHENIA GRAVIS
• Kearns-Sayre Syndrome Minus: Two Cases of Identical Large-Scale Mitochondrial DNA Deletions with Presentations outside the Classical Triad
• Kearns-Sayre syndrome with a novel large-scale deletion: a case report
• Kearns-Sayre Syndrome With Persistent Ventricular Tachycardia Refractory to Shocks and Medications
• Kearns-Sayre syndrome with rare imaging finding of SLC25A4 Mutation
• Kearns-Sayre Syndrome: a rare mitochondrial cytopathy complicated with complete heart block in a teenager
• Kearns-Sayre syndrome: expanding spectrum of a "novel" mitochondrial leukomyeloencephalopathy
• Kearns-Sayre syndrome: Two case reports and a review for the primary care physician
• Kidney manifestations of mitochondrial disorders
• Lady in red: A case of Kearns-Sayre syndrome supported by histopathology
• Low Prevalence of Cardiomyopathy in Patients with Mitochondrial Disease and Neurological Manifestations
• Magnetic resonance imaging pattern recognition in childhood bilateral basal ganglia disorders
• Management of Ptosis in Kearns-Sayre Syndrome: A Case Report and Literature Review
• Mitochondrial Ataxias: Molecular Classification and Clinical Heterogeneity
• Mitochondrial augmentation of hematopoietic stem cells in children with single large-scale mitochondrial DNA deletion syndromes
• Mitochondrial disorders: Understanding mitochondrial DNA point mutations and deletion syndromes
• Mitochondrial Dysfunction in Kidney Tubulopathies
• Mitochondrial Retinopathies
• Mitochondrial Retinopathy
• Myocardial and Arrhythmic Spectrum of Neuromuscular Disorders in Children
• Neuropathic Pain as Main Manifestation of <em>POLG</em>-Related Disease: A Case Report
• Nutrition rehabilitation-related complications in primary mitochondrial disorders
• Nutritional issues in a diabetic patient with Kearns-Sayre syndrome
• Ocular involvement in Kearns-Sayre syndrome
• Ophthalmologic school-based screening revealing Kearns-Sayre syndrome: a case report
• Ophthalmoplegia, pigmentary retinopathy, and abnormal cardiac conduction: A rare case of Kearns-Sayre syndrome
• Overlap between ophthalmology and psychiatry - A narrative review focused on congenital and inherited conditions
• Pearson syndrome: a multisystem mitochondrial disease with bone marrow failure
• Pediatric endothelial keratoplasty: a systematic review and individual participant data meta-analysis
• Pediatric single large-scale mtDNA deletion syndromes: The power of patient reported outcomes
• Phenotypic spectrum and clinical course of single large-scale mitochondrial DNA deletion disease in the paediatric population: a multicentre study
• Potpourri of retinopathies in rare eye disease - A case series
• Prevention of sudden death in Kearns-Sayre syndrome requires prospective studies
• Progressive external ophthalmoplegia
• Progressive External Ophthalmoplegia in Polish Patients-From Clinical Evaluation to Genetic Confirmation
• Progressive involvement of cardiac conduction system in paediatric patients with Kearns-Sayre syndrome: how to predict occurrence of complete heart block and sudden cardiac death?
• Propofol and Kearns-Sayre Syndrome: An idiographic approach
• Psychiatric Morbidities in Kearns Sayre Syndrome
• Ptosis Correction
• Ptosis Correction
• Rare cause of persistent hypocalcaemia in infancy due to PTH gene mutation
• Re: Propofol in Triple Trouble Kearns-Sayre Syndrome, Dyggve-Melchior-Clausen Syndrome, and Chromosome-9 Inversion
• Reply to: "Is the spinal cord truly affected in half of the patients with Kearns-Sayre syndrome?" and "Spinal cord and heart involvement in Kearns Sayre Syndrome: which link?"
• REPLY: The more comorbidities present, the more likely it is Kearns-Sayre syndrome than myasthenia
• Response to comments on: Diagnosis of Kearns-Sayre syndrome requires genetic confirmation
• Response to Finsterer's "Exclude hereditary and acquired differential disorders before attributing retinoschisis to Kears-Sayre syndrome"
• Retinal Manifestations of Mitochondrial Oxidative Phosphorylation Disorders
• Should Patients with Kearns-Sayre Syndrome and Corneal Endothelial Failure Be Genotyped for a <em>TCF4</em> Trinucleotide Repeat, Commonly Associated with Fuchs Endothelial Corneal Dystrophy?
• Should Patients with Kearns-Sayre Syndrome and Corneal Endothelial Failure Be Genotyped for a TCF4 Trinucleotide Repeat, Commonly Associated with Fuchs Endothelial Corneal Dystrophy?
• Stroke-like Episodes in Inherited Neurometabolic Disorders
• The arrhythmic risk in Kearns-Sayre syndrome: still many questions unanswered
• The arrhythmic risk in Kearns-Sayre syndrome: still many questions unanswered-Authors' reply
• The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions
• The more comorbidities present, the more likely it is Kearns-Sayre syndrome than myasthenia
• The Phenotypic Spectrum of 47 Czech Patients with Single, Large-Scale Mitochondrial DNA Deletions
• Understanding the impact of pediatric single large-scale mtDNA deletion syndromes on caregivers: Burdens and challenges
• Ventricular arrhythmias in Kearns-Sayre syndrome: A cohort study using the National Inpatient Sample database 2016-2019
• Whole Mitochondrial Genome Analysis in Turkish Patients with Mitochondrial Diseases
• Wide diagnostic and genotypic spectrum in patients with suspected mitochondrial disease