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Publications by Catherine Glatz

Mutation in the Mitochondrial tRNAVal Causes Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes

Mitochondrion

English

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Gastro-Intestinal Involvement in M.3243A>G-Associated Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes

Internal Medicine

Medicine

2018

English

Fixation-Off Sensitivity in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) Syndrome

Seizure : the journal of the British Epilepsy Association

Medicine

Neurology

2019

English

Anesthetic Considerations in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome: A Case Series

Canadian Journal of Anaesthesia

English

Spectral-Domain Optical Coherence Tomography in Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes

Canadian Journal of Ophthalmology

Medicine

Ophthalmology

2015

English

Wolff-Parkinson-White Syndrome in a Patient With Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome Mimicking Juvenile Myoclonic Epilepsy

Journal of Clinical Neurology (Korea

Neurology

2018

English

Sigmoid Volvulus in a Patient With Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS): A Rare Occurrence

BMJ Case Reports

Medicine

2016

English

Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes: A Unique Late Onset Presentation and Subsequent Management on a Symptomatic Basis

American Medical Student Research Journal

2015

English

Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population

American Journal of Human Genetics

Genetics

1998

English

Correlation of Serum Biomarkers and Magnetic Resonance Spectroscopy in Monitoring Disease Progression in Patients With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Due to mtDNA A3243G Mutation

Frontiers in Neurology

Neurology

2018

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Catherine Glatz

Mutation in the Mitochondrial tRNAVal Causes Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes

Related publications

Gastro-Intestinal Involvement in M.3243A>G-Associated Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes

Fixation-Off Sensitivity in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) Syndrome

Anesthetic Considerations in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome: A Case Series

Spectral-Domain Optical Coherence Tomography in Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes

Wolff-Parkinson-White Syndrome in a Patient With Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome Mimicking Juvenile Myoclonic Epilepsy

Sigmoid Volvulus in a Patient With Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS): A Rare Occurrence

Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes: A Unique Late Onset Presentation and Subsequent Management on a Symptomatic Basis

Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population

Correlation of Serum Biomarkers and Magnetic Resonance Spectroscopy in Monitoring Disease Progression in Patients With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Due to mtDNA A3243G Mutation