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Mitochondrial disease

  • Leigh Disease Associated with a Novel Mitochondrial DNA ND5 Mutation

    Leigh Disease Associated with a Novel Mitochondrial DNA ND5 Mutation

  • Consensus-Based Statements for the Management of Mitochondrial Stroke-Like Episodes[Version 1; Peer Review: 2 Approved]

    Consensus-Based Statements for the Management of Mitochondrial Stroke-Like Episodes[Version 1; Peer Review: 2 Approved]

  • Understanding and Coping with Mitochondrial Disease

    Understanding and Coping with Mitochondrial Disease

  • How Do We Manage Stroke-Like Episodes?

    How Do We Manage Stroke-Like Episodes?

  • Migraines: Genetic Studies Pietro Cortelli Mirella Mochi and Some Practical Considerations

    Migraines: Genetic Studies Pietro Cortelli Mirella Mochi and Some Practical Considerations

  • What Are Mitochondria and Mitochondrial Disease? What Does It Mean for Dysautonomia?

    What Are Mitochondria and Mitochondrial Disease? What Does It Mean for Dysautonomia?

  • Predisposition to Infection and SIRS in Primary Mitochondrial Disorders: 8 Years’ Experience in an Academic Center

    Predisposition to Infection and SIRS in Primary Mitochondrial Disorders: 8 Years’ Experience in an Academic Center

  • Summary – Pain Dr. Irina Anselm

    Summary – Pain Dr. Irina Anselm

  • MITOCHONDRIAL News

    MITOCHONDRIAL News

  • Diagnosis of Mitochondrial Diseases: Clinical and Histological Study of Sixty Patients with Ragged Red Fibers

    Diagnosis of Mitochondrial Diseases: Clinical and Histological Study of Sixty Patients with Ragged Red Fibers

  • Lennox-Gastaut Syndrome in Mitochondrial Disease

    Lennox-Gastaut Syndrome in Mitochondrial Disease

  • 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

  • A Novel Mitochondrial DNA Deletion in a Chinese Girl with Kearns-Sayre

    A Novel Mitochondrial DNA Deletion in a Chinese Girl with Kearns-Sayre

  • Hope. Energy. Life

    Hope. Energy. Life

  • Deletion in Blood Mitochondria1 DNA in Kearns-Sayre Syndrome

    Deletion in Blood Mitochondria1 DNA in Kearns-Sayre Syndrome

  • Epilepsy and Mitochondrial Dysfunction: ª the Author(S) 2017 DOI: 10.1177/2326409817733012 a Single Center’S Experience Journals.Sagepub.Com/Home/Iem

    Epilepsy and Mitochondrial Dysfunction: ª the Author(S) 2017 DOI: 10.1177/2326409817733012 a Single Center’S Experience Journals.Sagepub.Com/Home/Iem

  • Diagnosis and Management of Mitochondrial Disease: a Consensus Statement from the Mitochondrial Medicine Society

    Diagnosis and Management of Mitochondrial Disease: a Consensus Statement from the Mitochondrial Medicine Society

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

    Mitochondrial Diseases in North America an Analysis of the NAMDC Registry

Top View
  • Section 1: Adults with Mitochondrial Myopathy Data Collected in Questions 1 and 2 Were Used to Identify Respondents and Are Not Included in This Report
  • Patient Care Standards for Primary Mitochondrial Disease: a Consensus Statement from the Mitochondrial Medicine Society
  • Diagnostic Approach in Infants and Children with Mitochondrial Diseases Ching-Shiang Chi*
  • Mitochondrial Disorders the New Frontier
  • Clinical Reasoning: Encephalopathy in a 10-Year-Old Boy Lance Rodan and Ingrid Tein Neurology 2012;79;E12-E18 DOI 10.1212/WNL.0B013e31825fdf51
  • Investigation of Mitochondrial Disease on September 23, 2021 by Guest
  • Epilepsy Guidelines
  • Factsheet: Mitrochondrial Disease Specialized Health Needs Interagency Collaboration
  • Metabolic Profiling Indicates Impaired Pyruvate Dehydrogenase Function in Myalgic Encephalopathy/Chronic Fatigue Syndrome
  • Molecular Bases of Hearing Loss in Multi-Systemic Mitochondrial
  • Mitochondrial Causes of Epilepsy: Evaluation, Diagnosis, and Treatment
  • Review the Development of Mitochondrial Medicine
  • An Isolated Complex V Inefficiency and Dysregulated Mitochondrial
  • The Impact of Mitochondrial Deficiencies in Neuromuscular
  • Gene Variants, Mitochondria and Autoimmunity in ME/CFS and Fibromyalgia
  • Mitochondrial Disorders: Analysis of Their Clinical and Imaging Characteristics
  • Mitochondrial Myopathies
  • Epigenetics and Migraine; Complex Mitochondrial Interactions Contributing to Disease Susceptibility


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