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Mitochondrial disease
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]
Understanding and Coping with Mitochondrial Disease
How Do We Manage Stroke-Like Episodes?
Migraines: Genetic Studies Pietro Cortelli Mirella Mochi and Some Practical Considerations
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
Summary – Pain Dr. Irina Anselm
MITOCHONDRIAL News
Diagnosis of Mitochondrial Diseases: Clinical and Histological Study of Sixty Patients with Ragged Red Fibers
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
A Novel Mitochondrial DNA Deletion in a Chinese Girl with Kearns-Sayre
Hope. Energy. Life
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
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
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
Mitochondrial Syndromes Revisited
Mitochondrial Disease and Anesthesia ª the Author(S) 2017 DOI: 10.1177/2326409817707770 Journals.Sagepub.Com/Home/Iem
Stroke-Like Episodes in Adult Mitochondrial Disease: Investigation and Management
Epilepsy in a Mitochondrial Disorder
A Systematic Review of Mitochondrial Abnormalities in Myalgic
Diagnosis and Management of Mitochondrial Disease: a Consensus Statement from the Mitochondrial Medicine Society
A Case of MELAS Syndrome with Typical Cluster Headache
Management of Occupational Exposures to HBV, HCV, &
Brief Genetics Report Defining the Importance of Mitochondrial Gene Defects in Maternally Inherited Diabetes by Sequencing the Entire Mitochondrial Genome Alan T.W
The Mitochondrion and Its Disorders
M Ito Chondrial D Isease Fact Sheet
Kearns Sayer Syndrome- a Case Report
Revisiting Mitochondrial Diagnostic Criteria in the New Era of Genomics
MELAS Syndrome): Diagnostic Criteria, Features of Epileptic Seizures and Treatment Approaches
Molecular Basis of Leigh Syndrome: a Current Look Manuela Schubert Baldo* and Laura Vilarinho
Mitochondrial DNA Variants Correlate with Symptoms in Myalgic
Therapeutic Approaches to Treat Mitochondrial Diseases: “One-Size-Fits-All” and “Precision Medicine” Strategies
Mitochondrial Disease: an Uncommon but Important Cause of Diabetes Mellitus
Non-Ischemic Scar Underlines Ventricular Arrhythmias in Kearns
How to Spot Mitochondrial Disease in Adults
Epilepsy in Adults with Mitochondrial Disease: a Cohort Study
Kearns-Sayre Syndrome Presenting As Somatomedin C Deficiency and Complete Heart Block
Clinical Manifestations and Anesthetic Management of Kearns-Sayre Syndrome -A Case Report
Epilepsy in Mitochondrial Diseases—Current State of Knowledge on Aetiology and Treatment
The Neurologic Manifestations of Mitochondrial Disease
Kearns Sayre Syndrome: a Mitochondrial Disorder
Warning Signs of a Stroke-Like Episode
Investigating Fatigue and Exercise Intolerance in a University Immunology Clinic
Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) Genetic Testing