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Diabetes and deafness

  • Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G Heterogeneidade Fenotípica De Uma Família Causada

    Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G Heterogeneidade Fenotípica De Uma Família Causada

  • Identification of P.A684V Missense Mutation in the WFS1 Gene As a Frequent Cause of Autosomal Dominant Optic Atrophy and Hearing

    Identification of P.A684V Missense Mutation in the WFS1 Gene As a Frequent Cause of Autosomal Dominant Optic Atrophy and Hearing

  • Maternally Inherited Diabetes and Deafness (MIDD) Syndrome with M.3243A>G Mutation Associated with Renal Failure — a Case Report

    Maternally Inherited Diabetes and Deafness (MIDD) Syndrome with M.3243A>G Mutation Associated with Renal Failure — a Case Report

  • The Role of Mitochondrial Mutations and Chronic Inflammation in Diabetes

    The Role of Mitochondrial Mutations and Chronic Inflammation in Diabetes

  • Mitochondrial Diseases in North America an Analysis of the NAMDC Registry

    Mitochondrial Diseases in North America an Analysis of the NAMDC Registry

  • Maternally Inherited Diabetes and Deafness Presenting with Ptosis and Macular Pattern Dystrophy Olufunmilola Ogun, Claire Sheldon and Jason J.S

    Maternally Inherited Diabetes and Deafness Presenting with Ptosis and Macular Pattern Dystrophy Olufunmilola Ogun, Claire Sheldon and Jason J.S

  • Frequency and Clinical Features of Patients with Sensorineural Hearing Loss Associated with the A3243G Mutation of the Mitochondrial DNA in Otorhinolaryngic Clinics

    Frequency and Clinical Features of Patients with Sensorineural Hearing Loss Associated with the A3243G Mutation of the Mitochondrial DNA in Otorhinolaryngic Clinics

  • Diabetes and Deafness; Not All MODY Is MELAS

    Diabetes and Deafness; Not All MODY Is MELAS

  • Overview on Visceral Manifestations of Mitochondrial Disorders

    Overview on Visceral Manifestations of Mitochondrial Disorders

  • The Effects of Coenzyme Q10 Treatment on Maternally Inherited Diabetes Mellitus and Deafness, and Mitochondrial DNA 3243 (A to G) Mutation

    The Effects of Coenzyme Q10 Treatment on Maternally Inherited Diabetes Mellitus and Deafness, and Mitochondrial DNA 3243 (A to G) Mutation

  • Molecular Bases of Hearing Loss in Multi-Systemic Mitochondrial

  • Identification of Novel Mutations of the WFS1 Gene in Brazilian Patients with Wolfram Syndrome

  • Met5. Mitochondrial Disorders.Pdf

  • Mitochondrial Syndromes Revisited

    Mitochondrial Syndromes Revisited

  • Mitochondrial Diabetes Molecular Mechanisms and Clinical Presentation J

  • Leigh Syndrome in a Pedigree Harboring the M.1555A>G Mutation

    Leigh Syndrome in a Pedigree Harboring the M.1555A>G Mutation

  • And Cell-Type–Specific Manifestations of Heteroplasmic Mtdna

    And Cell-Type–Specific Manifestations of Heteroplasmic Mtdna

  • Design, Development and Deployment of a Web-Based Interoperable Registry for Inherited Retinal Dystrophies in Portugal: the IRD

    Design, Development and Deployment of a Web-Based Interoperable Registry for Inherited Retinal Dystrophies in Portugal: the IRD

Top View
  • Heterogeneous Phenotypic Manifestations of Maternally
  • MIDD Or Maternally Inherited Diabetes & Deafness
  • An Example of Monogenic Diabetes Mellitus
  • Mitochondria P F Chinnery, E a Schon
  • Mitochondrial Disease and Endocrine Dysfunction Jasmine Chow1
  • MT-TK Gene Mitochondrially Encoded Trna Lysine
  • Brief Genetics Report Defining the Importance of Mitochondrial Gene Defects in Maternally Inherited Diabetes by Sequencing the Entire Mitochondrial Genome Alan T.W
  • Mitochondrial Disorders and the Eye
  • Loss-Of-Function Mutation in Thiamine Transporter 1 in a Family with Autosomal Dominant Diabetes
  • Mitochondrial DNA
  • Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches
  • Maternally Inherited Diabetes and Deafness and Mitochondrial Encephalopathy Lactic Acidosis and Stroke Like Episodes
  • Maternally Inherited Diabetes and Deafness
  • Download Information Pack
  • MT-TL1 Gene Mitochondrially Encoded Trna Leucine 1 (UUA/G)


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