Disease: Maternally inherited diabetes and deafness
- A Novel Mutation of Mitochondrial T14709C Causes Myoclonic Epilepsy with Ragged Red Fibers Syndrome in a Chinese Patient
- A Patient with Mitochondrial Disease on Dialysis with Long-term Follow-up of Cardiomyopathy: An Autopsy Case Report
- A retrospective cohort study exploring the association between different mitochondrial diseases and hearing loss
- A single-arm, open-label, intervention study to investigate the improvement of glucose tolerance after administration of the 5-aminolevulinic acid (5-ALA) in the patients with mitochondrial diabetes mellitus
- Association between maternally inherited deafness, epilepsy, and intellectual disability and the m.12207G > A <em>MT-TS2</em> pathogenic variant in a Japanese family
- Audiological and Vestibular Findings in Subjects with MELAS Syndrome
- Bilateral deafness, diabetes, and different types of cardiomyopathy in family members with m.3243A > g mutation: a case report
- Case report: mitochondrial diabetes mellitus in a Chinese family due to m.3243A>G
- Cerebellar vermis hypoplasia and bilateral basal ganglia calcification in maternally inherited diabetes and deafness
- Choroidal neovascularization associated with butterfly-shaped pattern dystrophy - a case report
- Chronic intestinal psuedo-obstruction and MIDD, a rare cause of acute abdomen: implications in emergency surgery
- Chronic kidney disease caused by maternally inherited diabetes and deafness: a case report
- Chronological change of left ventricular global longitudinal strain in patients with maternally inherited diabetes and deafness: A case series
- Clinical Characteristics of Diabetes in People with Mitochondrial DNA 3243A>G Mutation in Korea
- Clinical phenotype of mitochondrial diabetes due to rare mitochondrial DNA mutations
- Comment on Progression of Retinopathy Secondary to Maternally Inherited Diabetes and Deafness: Evaluation of Predicting Parameters
- Commentary: Heteroplasmy in maternally inherited diabetes and deafness
- Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients
- Comments on: Outer retinal tubulation and inner retinal pseudocysts in a patient with maternally inherited diabetes and deafness evaluated with optical coherence tomography angiogram
- Concomitant Mitochondrial Diabetes and Myopathy Mistook for Complications of Immunosuppressants After Kidney Transplant
- De Novo Mutation of m.3243A>G together with m.16093T>C Associated with Atypical Clinical Features in a Pedigree with MIDD Syndrome
- Diabetes Out-of-the-Box: Diabetes Mellitus and Impairment in Hearing and Vision
- Diabetes, deafness and renal disease
- Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report
- Effective treatment of choreaballism due to an <em>MT-CYB</em> variant with haloperidol, tetrabenazine, and antioxidants
- Effects of novel antidiabetes agents on apoptotic processes in diabetes and malignancy: Implications for lowering tissue damage
- Efficacy of GLP-1 Agonist Therapy in Autosomal Dominant WFS1-Related Disorder: A Case Report
- Etiologic distribution and clinical characteristics of pediatric diabetes in 276 children and adolescents with diabetes at a single academic center
- Factors associated with skin graft take in fibula and radial forearm free flap donor sites
- Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G
- Five non-mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes phenotype adult patients with m.3243A>G mutation after kidney transplantation: follow-up and review of the literature
- Fundus Autofluorescence in Maternally Inherited Diabetes and Deafness: The Gold Standard for Monitoring Maculopathy?
- Gene Panel Sequencing of Patients With Monogenic Diabetes Brings to Light Genes Typically Associated With Syndromic Presentations
- Genetic testing for misclassified monogenic diabetes in Māori and Pacific peoples in Aōtearoa New Zealand with early-onset type 2 diabetes
- Glucagon-like peptide-1 receptor agonists (GLP1-RA) in the treatment of mitochondrial diabetes
- Heteroplasmy Detection of Mitochondrial DNA A3243G Mutation Using Quantitative Real-Time PCR Assay Based on TaqMan-MGB Probes
- Identification of eight genomic protective alleles for mitochondrial diabetes by Kinship-graph convolutional network
- Imeglimin-mediated glycemic control in maternally inherited deafness and diabetes
- Increased Peripheral Blood Heteroplasmy of the mt.3243A>G Mutation Is Associated with Earlier End-Stage Kidney Disease: A Case Report and Review of the Literature
- Intravitreal bevacizumab in cystoid macular edema associated to maternally inherited diabetes and deafness's macular dystrophy
- Late onset of type 2 diabetes is associated with mitochondrial tRNA<sup>Trp</sup> A5514G and tRNA<sup>Ser(AGY)</sup> C12237T mutations
- Letter to the Editor: Maternally Inherited Diabetes and Deafness is Not Only Biorgan but Multiorgan
- Macrocytosis in Mitochondrial DNA Deletion Syndromes
- Macular findings expedite accurate diagnosis of MIDD in a young female patient with newly diagnosed diabetes
- Maternally Inherited Diabetes and Deafness (MIDD) - Atypical Clinical Diabetes Features Leading to the Diagnosis
- Maternally inherited diabetes and deafness coexists with lipoprotein lipase gene mutation-associated severe hyperlipidemia that was resistant to fenofibrate and atorvastatin, but sensitive to bezafibrate: A case report
- Maternally inherited diabetes and deafness complicated by mesangial galactose-deficient IgA1 deposits: a case report
- Maternally Inherited Diabetes and Deafness in 4 Family Members with DNA Mutation and at Least 4 Generations with Suggestive Disease Phenotype
- Maternally inherited diabetes and deafness with a variable presentation across three generations within a pedigree, South Africa
- MELAS Syndrome and MIDD Unmasked by Metformin Use: A Case Report
- Mitochondrial disease: an uncommon but important cause of diabetes mellitus
- Mitochondrial Disorder: Maternally Inherited Diabetes and Deafness
- Mitochondrial Retinopathy
- Monogenic Diabetes: Genetics and Relevance on Diabetes Mellitus Personalized Medicine
- mTOR inhibitors may benefit kidney transplant recipients with mitochondrial diseases
- Multimodal analysis in symptomatic MIDD-associated retinopathy. A case report and literature review
- Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation
- Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation
- Mutational Analysis of Mitochondrial tRNA Genes in 200 Patients with Type 2 Diabetes Mellitus
- OCT-Angiography analysis in a case of maternally inherited diabetes and deafness
- One mutation, three phenotypes: novel metabolic insights on MELAS, MIDD and myopathy caused by the m.3243A > G mutation
- Optical coherence tomography, angiography and conventional multimodal imaging findings in a case of maternally inherited diabetes and deafness
- Outer retinal tubulation and inner retinal pseudocysts in a patient with maternally inherited diabetes and deafness evaluated with optical coherence tomography angiogram
- Outer retinal tubulations in maternally inherited diabetes & deafness - associated macular dystrophy: case report
- Penetrance and expressivity of mitochondrial variants in a large clinically unselected population
- Pilot Trial on the Effect of 5-Aminolevulinic Acid on Glucose Tolerance in Patients with Maternally Inherited Diabetes and Deafness
- Predicting the future: Diabetes and Brexit
- Progression of Peripheral Vestibular Dysfunctions in Patients With a Mitochondrial A3243G Mutation
- Progression of Retinopathy Secondary to Maternally Inherited Diabetes and Deafness - Evaluation of Predicting Parameters
- Proteomic Analysis of m.8296A>G Variation in the Mitochondrial <em>tRNA</em> <sup>Lys</sup> Gene
- Renal manifestations in adults with mitochondrial disease from the mtDNA m.3243A>G pathogenic variant
- Reply to Comment on: Progression of Retinopathy Secondary to Maternally Inherited Diabetes and Deafness - Evaluation of Predicting Parameters
- Response to comments on: Outer retinal tubulation and inner retinal pseudocysts in a patient with maternally inherited diabetes and deafness evaluated with optical coherence tomography angiogram
- Retinal Manifestations of Mitochondrial Oxidative Phosphorylation Disorders
- Retinal Pigment Abnormalities in a Woman With Diabetes
- Role of mitochondrial DNA in diabetes Mellitus Type I and Type II
- Screening and prevalence of cardiac abnormalities on electro- and echocardiography in a large cohort of patients with mitochondrial disease
- Sensitive quantification of m.3243A>G mutational proportion in non-retinal tissues and its relationship with visual symptoms
- Six-year prospective follow-up study in 151 carriers of the mitochondrial DNA 3243 A>G variant
- Sleep-Disordered Breathing in Adult Patients With Mitochondrial Diseases: A Cohort Study
- Structural Features Associated With the Development and Progression of RORA Secondary to Maternally Inherited Diabetes and Deafness
- Subliminal Message Outer Retinal Tubulations Resembling Mitochondria in Maternally Inherited Diabetes and Deafness
- Successful transcatheter mitral valve repair for functional mitral regurgitation in a patient with mitochondrial cardiomyopathy: a case report
- T cell activation contributes to purifying selection against the MELAS-associated m.3243A>G pathogenic variant in blood
- The Association between Nutritional Status and In-Hospital Mortality among Patients with Acute Coronary Syndrome-A Result of the Retrospective Nutritional Status Heart Study (NSHS)
- The clinical and genetic characteristics of maternally inherited diabetes and deafness (MIDD) with mitochondrial m.3243A > G mutation: A 10-year follow-up observation study and literature review
- The clinical and genetic characteristics of maternally inherited diabetes and deafness (MIDD) with mitochondrial m.3243A > G mutation: A 10-year follow-up observation study and literature review
- The genomic mosaic of mitochondrial dysfunction: Decoding nuclear and mitochondrial epigenetic contributions to maternally inherited diabetes and deafness pathogenesis
- The heart in m.3243A>G carriers
- The Mutations and Clinical Variability in Maternally Inherited Diabetes and Deafness: An Analysis of 161 Patients
- THE ROLE OF HETEROPLASMY IN THE DIAGNOSIS AND MANAGEMENT OF MATERNALLY INHERITED DIABETES AND DEAFNESS
- The Role of Mitochondrial Mutations and Chronic Inflammation in Diabetes
- The Spectrum of Maculopathy in Mitochondrial DNA A3243G Mutation: A Case Series of Six Patients
- The Tip of the Iceberg in Maternally Inherited Diabetes and Deafness
- The West of Scotland Cohort of Mitochondrial Individuals with the m.3243A>G Variant: Variations in Phenotypes and Predictors of Disease Severity
- Treating hypercholesterinemia in a patient with maternally inherited diabetes and deafness (MIDD) by the proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor alirocumab
- tRNA derived fragments are altered in diabetes
- tRNA-derived fragments are altered in diabetes
- Urinary Tract Involvement in Wolfram Syndrome: A Narrative Review
- Variants m.13276G>A in the MT-ND5 and m.8241T>G in the MT-CO2 gene are not responsible for maternally inherited diabetes and deafness