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Case report

First published 2017

Early Infantile Leigh-like SLC19A3 Gene Defects Have a Poor Prognosis: Report and Review

Majid Alfadhel

Journal of Central Nervous System Disease

Retricted access

Research article

First published 2015-7

MEGDEL Syndrome in a Child From Palestine

Imad M. Dweikat, Samer Abdelrazeq, Suhail Ayesh [...]

Journal of Child Neurology

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Other

First published 2009-07

Mutations in ND Subunits of Complex I Are an Important Genetic Cause of Childhood Mitochondrial Encephalopathies

Byung Chan Lim, Jun Dong Park, Hee Hwang [...]

Journal of Child Neurology

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Research article

First published 2017-4

A MELAS phenotype is not necessarily MELAS

Josef Finsterer, Sinda Zarrouk-Mahjoub

Tropical Doctor

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Research article

First published 1999-07

Acute or Subacute Cranial Computed Tomography Findings in Patients with Congenital Lactic Acidemia

Galen N. Breningstall

Clinical Pediatrics

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Case report

First published 2025

Expanding the Epidemiological and Phenotypic Spectrum of MEGDEL Syndrome: The First Case Report From Egypt

Abdelrahim A. Sadek, Mohammed A. Aladawy, Tarek MM. Mansour [...]

Clinical Medicine Insights: Pediatrics

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Other

First published 1998-11

A Large-Scale Mitochondrial DNA Deletion Causing Progressive Ataxia

Shigeko Saitoh, Mariko Y. Momoi, Takehiro Ohki [...]

Journal of Child Neurology

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Research article

First published 2022-3

Clinical and molecular spectrum associated with Polymerase-γ related disorders

Ruchika Jha, Harshkumar Patel, Rachana Dubey [...]

Journal of Child Neurology

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Research article

First published 2017-2

A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement Disorder

Caterina Garone, Juliana Gurgel-Giannetti, Simone Sanna-Cherchi [...]

Journal of Child Neurology

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Research article

First published 2004-8

Diffusion magnetic resonance imaging patterns in metabolic and toxic brain disorders

R. N. Sener

Acta Radiologica

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