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Research article

First published 2013-10

The Role of Brain MRI in Mitochondrial Neurogastrointestinal Encephalomyopathy

Mauro Scarpelli, Giuseppe Kenneth Ricciardi, Alberto Beltramello [...]

The Neuroradiology Journal

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Other

First published 2007-07

Mitochondrial Encephalomyopathy Due to a Novel Mutation in the tRNAGlu of Mitochondrial DNA

Jacklyn Pancrudo, Sara Shanske, Eduardo Bonilla [...]

Journal of Child Neurology

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Research article

First published 1995-10

Mitochondrial Encephalomyopathy: A Rare Genetic Cause of Sensorineural Hearing Loss

Thomas J. Donovan

Annals of Otology,Rhinology & Laryngology

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Other

First published 1999-11

Does the Patient Have a Mitochondrial Encephalomyopathy?

Salvatore DiMauro, Eduardo Bonilla, Darryl C. De Vivo

Journal of Child Neurology

Open access

Research article

First published 2024-03

Meningoencephalitis in a novel mutation in MNGIE (mitochondrial neurogastrointestinal encephalomyopathy) ending a familial diagnostic odyssey: A case series report

Noor Redha, Zahra Al-Sahlawi, Hasan Hasan [...]

Journal of Central Nervous System Disease

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Research article

First published 2014-9

Phenotypic Analysis of Epilepsy in the Mitochondrial Encephalomyopathy,Lactic Acidosis,and Strokelike Episodes–Associated Mitochondrial DNA A3243G Mutation

Scott T. Demarest, Matthew T. Whitehead, Sinan Turnacioglu [...]

Journal of Child Neurology

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Research article

First published 2013-2

A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene ( MTCYB) in a Patient With Mitochondrial Encephalomyopathy,Lactic Acidosis,and Strokelike Episodes Syndrome

Valentina Emmanuele, Evangelia Sotiriou, Purificación Gutierrez Rios [...]

Journal of Child Neurology

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Other

First published 2005-02

Episodic Hyponatremia in Mitochondrial Encephalomyopathy,Lactic Acidosis,and Strokelike Episodes (MELAS)

Hiroaki Kubota, Yuzo Tanabe, Jun-ichi Takanashi [...]

Journal of Child Neurology

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Other

First published 2002-01

Diffuse Magnetic Resonance Imaging White-Matter Changes in a 15-Year-Old Boy With Mitochondrial Encephalomyopathy

Arie Weinstock, Pierre Giglio, Michael E. Cohen [...]

Journal of Child Neurology

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Case report

First published 2025-7

Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE) Phenotype Associated With Unique Compound Heterozygous POLG Variants: Case Presentation and Review of the Literature

Laura S. Finn, Amy Goldstein, Holly L. Hedrick

Pediatric and Developmental Pathology

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