- Home
- » Tags
- » Leigh syndrome
Top View
- The ATP Synthase Deficiency in Human Diseases
- The Evolution of Leigh Syndrome Mary Kay Koenig, MD
- Clinical Trials in Mitochondrial Disease: ª the Author(S) 2017 DOI: 10.1177/2326409817733013 an Update on EPI-743 and RP103 Journals.Sagepub.Com/Home/Iem
- Autosomal Dominant Optic Atrophy Plus Syndrome
- Hereditary Spastic Paraplegias: Time for an Objective Case Definition And
- Leigh Syndrome
- Mitochondrial Ribosomal Proteins: Candidate Genes for Mitochondrial Disease James E
- Imaging Findings and Clinical Perspectives of Acute Necrotising
- Mitochondrial Causes of Epilepsy: Evaluation, Diagnosis, and Treatment
- Leigh Syndrome with Atypical Cerebellar Lesions
- Motor Neuron Syndrome As a New Phenotypic Manifestation of Mutation 9185T>C in Gene MTATP6
- Molecular Genetics and Metabolism Xxx (Xxxx) Xxx–Xxx
- Peripheral Neuropathy with Ataxia in Childhood As a Result of the G8363A Mutation in Mitochondrial DNA
- Blueprint Genetics Migraine Panel
- Clinical Insights Into Mitochondrial Neurodevelopmental and Neurodegenerative Disorders: Their Biosignatures from Mass Spectrometry-Based Metabolomics
- Diagnosis of Inherited Metabolic Disorders Affecting the Nervous System
- Mitochondrial Disorders: Analysis of Their Clinical and Imaging Characteristics
- Blueprint Genetics Spinal Muscular Atrophy Panel
- EPI-743 for Mitochondrial Disease – First Line
- PTC743 Mitochondrial Epilepsy Trial
- Differential Diagnosis of Chorea
- Diagnosis and Management of Mitochondrial Disease: a Consensus Statement from the Mitochondrial Medicine Society
- A Mitochondrial Encephalomyopathy with a Partial Cytochrome C Oxidase Deficiency of Muscle
- Whole Exome Sequencing in a Child with Acute Disseminated Encephalomyelitis, Optic Neuritis, and Periodic Fever Syndrome: a Case Report Pablo A
- Psychosis in Leigh Syndrome T
- Leigh Syndrome and Mitochondrial Encephalopathy Precision Panel
- Mitochondrial Syndromes with Leukoencephalopathies
- Leigh Syndrome: One Disorder, More Than 75 Monogenic Causes
- Monogenic Diseases Masquerading As Multiple Sclerosis
- Molecular Basis of Leigh Syndrome: a Current Look Manuela Schubert Baldo* and Laura Vilarinho
- Therapeutic Approaches to Treat Mitochondrial Diseases: “One-Size-Fits-All” and “Precision Medicine” Strategies
- Genetic Testing for Neuromuscular Disorders
- Mitochondrial DNA Mutations in Leigh Syndrome and Their Phylogenetic Implications
- Investigation Into the Effects and Mechanisms of Rapamycin Treatment
- A Rare Mitochondrial Disorder: Leigh Sydrome - a Case Report Dhananjay Y Shrikhande1, Piyush Kalakoti2*, MM Aarif Syed2, Kunal Ahya2, Gurmeet Singh1
- Epilepsy in Mitochondrial Diseases—Current State of Knowledge on Aetiology and Treatment
- The Neurologic Manifestations of Mitochondrial Disease
- Cytochrome C Oxidase Deficiency
- Leigh Syndrome Due to NDUFV1 Mutations Initially Presenting As LBSL
- This Student Paper Was Written As an Assignment in the Graduate Course
- A Flow Chart for the Evaluation of Chorea Ruth H
- Acute Movement Disorders in Childhood
- Cytochrome C Oxidase Deficiency Due to a Novel SCO2 Mutation Mimics Werdnig-Hoffmann Disease
- In the United States Court of Federal Claims
- Cerebral Manifestations of Mitochondrial Disorders
- The Mitochondrial 13513G>A Mutation Is Most Frequent in Leigh
- Leigh Syndrome Mimicking Wernicke's Encephalopathy: A