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First published 2011-3

Vanishing White Matter Disease Associated With Ptosis and Myoclonic Seizures

Suvasini Sharma, Ravindra Arya, K.N. Vykunta Raju [...]

Journal of Child Neurology

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Research article

First published 2007-04

Arg113His mutation of vanishing white matter is not present in multiple sclerosis

M. Lucas, R. Suarez, A. Marcos [...]

Multiple Sclerosis Journal

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First published 2008-02

Genetic and Clinical Heterogeneity in eIF2B-Related Disorder

Jelena Maletkovic, Raphael Schiffmann, J. Rafael Gorospe [...]

Journal of Child Neurology

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First published 2008-05

Letter to the Editor: No evidence for association between the EIF2B5 gene and multiple sclerosis in French families

A Fogli, C Barbier, I Cournu-Rebeix [...]

Multiple Sclerosis Journal

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First published 2007-06

Peripheral Neuropathy in a Child With Cree Leukodystrophy

R.J. Huntsman, S. Seshia, N. Lowry [...]

Journal of Child Neurology

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Research article

First published 2017-9

Postmortem Whole Exome Sequencing Identifies Novel EIF2B3 Mutation With Prenatal Phenotype in 2 Siblings

Hannah Song, Sina Haeri, Hannes Vogel [...]

Journal of Child Neurology

Open access

Review article

First published 2014

Vanishing White Matter Disease in a Spanish Population

Eulàlia Turón-Viñas, Mercè Pineda, Victòria Cusí [...]

Journal of Central Nervous System Disease

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First published 2003-09

Leukoencephalopathy With Vanishing White Matter: From Magnetic Resonance Imaging Pattern to Five Genes

Peter A. J. Leegwater, Jan C. Pronk, Marjo S. van der Knaap

Journal of Child Neurology

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Research article

First published 2013-11

Vanishing White Matter With Hepatomegaly and Hypertriglyceridemia Attacks

Ozlem Unal, Burce Ozgen, Diclehan Orhan [...]

Journal of Child Neurology

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