Disease: Noninsulin-dependent diabetes mellitus with deafness
- A mitochondrial origin for inherited diabetes mellitus
- 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
- Alström Syndrome with Early Vision and Hearing Impairement
- Alström syndrome: an ultra-rare monogenic disorder as a model for insulin resistance, type 2 diabetes mellitus and obesity
- Atypical Retinal Phenotype in a Patient With Alström Syndrome and Biallelic Novel Pathogenic Variants in <em>ALMS1</em>, Including a <em>de novo</em> Variation
- Awareness, Perceptions, and Literacy Surrounding Hearing Loss and Hearing Rehabilitation Among the Adult Population in the United States
- 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
- CHORIOCAPILLARIS SIGNAL VOIDS IN MATERNALLY INHERITED DIABETES AND DEAFNESS AND IN PSEUDOXANTHOMA ELASTICUM
- 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 and genetic analysis of two wolfram syndrome families with high occurrence of wolfram syndrome and diabetes type II: a case report
- Clinical Characteristics of Diabetes in People with Mitochondrial DNA 3243A>G Mutation in Korea
- Clinical Efficacy of Retroauricular Injection of Methylprednisolone Sodium Succinate in the Treatment of Sudden Deafness with Type 2 Diabetes
- Clinical phenotype of mitochondrial diabetes due to rare mitochondrial DNA mutations
- CO-OCCURRENCE OF NEPHRONOPHTHISIS TYPE 1 AND ALSTRÖM SYNDROME: A CASE REPORT
- 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
- Cystoid macular changes on optical coherence tomography in a patient with maternally inherited diabetes and deafness (MIDD)-associated macular dystrophy
- 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
- Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report
- Effects of novel antidiabetes agents on apoptotic processes in diabetes and malignancy: Implications for lowering tissue damage
- Etiologic distribution and clinical characteristics of pediatric diabetes in 276 children and adolescents with diabetes at a single academic center
- Evidence for gene-smoking interactions for hearing loss and deafness in Japanese American families
- Factors associated with skin graft take in fibula and radial forearm free flap donor sites
- Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G
- Fundus autofluorescence: the key in the diagnosis of maternally inherited diabetes and deafness
- Gene Panel Sequencing of Patients With Monogenic Diabetes Brings to Light Genes Typically Associated With Syndromic Presentations
- Genetic Factors of Diabetes
- Genetic testing for misclassified monogenic diabetes in Māori and Pacific peoples in Aōtearoa New Zealand with early-onset type 2 diabetes
- Genome-wide DNA methylation analysis of human peripheral blood reveals susceptibility loci of diabetes-related hearing loss
- Glucagon-like peptide-1 receptor agonists (GLP1-RA) in the treatment of mitochondrial diabetes
- Hypoparathyroidism, Sensorineural deafness and renal disease (Barakat syndrome) caused by a reduced gene dosage in GATA3: a case report and review of literature
- Identification of a missense variant in the WFS1 gene that causes a mild form of Wolfram syndrome and is associated with risk for type 2 diabetes in Ashkenazi Jewish individuals
- Identification of eight genomic protective alleles for mitochondrial diabetes by Kinship-graph convolutional network
- Identifying and visualising multimorbidity and comorbidity patterns in patients in the English National Health Service: a population-based study
- 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
- Kidney involvement in MELAS syndrome: Description of 2 cases
- 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
- 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 is a mitochondrial multiorgan disorder syndrome (MIMODS)
- Measuring gene-gene interaction using Kullback-Leibler divergence
- MELAS Syndrome and MIDD Unmasked by Metformin Use: A Case Report
- Metformin Reduces the Risk of Hearing Loss: A Retrospective Cohort Study
- Mitochondrial Disorder: Maternally Inherited Diabetes and Deafness
- Monogenic and syndromic diabetes due to endoplasmic reticulum stress
- 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
- Mutational Analysis of Mitochondrial tRNA Genes in 200 Patients with Type 2 Diabetes Mellitus
- New progress of IGF-1 and allosteroid injection in the treatment of sudden deafness complicated with type 2 diabetes
- Novel Mutations of the ALMS1 Gene in Patients with Alström Syndrome
- 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 tubulations in maternally inherited diabetes & deafness - associated macular dystrophy: case report
- Pancreatic stone protein/regenerating protein is a potential biomarker for endoplasmic reticulum stress in beta cells
- Phenotypic and Genetic Heterogeneity in a Thai Glucokinase MODY Family Reveals the Complexity of Young-Onset Diabetes
- Predicting the future: Diabetes and Brexit
- Prevention of progressive hearing loss in a mouse model of diabetes by oral intake of eicosapentaenoic acid ethyl ester
- Progression of Retinopathy Secondary to Maternally Inherited Diabetes and Deafness - Evaluation of Predicting Parameters
- 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
- Reply to Letter to the Editor "Maternally inherited diabetes and deafness is a mitochondrial multiorgan disorder syndrome (MIMODS)"
- 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
- 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
- Sensorineural Deafness After Spine Surgery: Case Series and Literature Review
- Sex-Specific Associations Between Diabetes Mellitus and Hearing Loss in the Middle-Aged and Elderly Individuals: A National Cohort Study of Chinese Adults
- Skin Pigmentation and Risk of Hearing Loss in Women
- 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
- 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 characteristics of patients with mitochondrial tRNA Leu(UUR)m.3243A > G mutation: Compared with type 1 diabetes and early onset type 2 diabetes
- The genetic and clinical characteristics of WFS1 related diabetes in Chinese early onset type 2 diabetes
- 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 ER Stress in Diabetes: Exploring Pathological Mechanisms Using Wolfram Syndrome
- 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 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
- 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
- Wolfram Syndrome 1: A Pediatrician's and Pediatric Endocrinologist's Perspective
- Wolfram Syndrome Type 2: A Systematic Review of a Not Easily Identifiable Clinical Spectrum