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Retricted access

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

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Research article

First published 2015-4

Adult-onset vanishing white matter disease as differential diagnosis of primary progressive multiple sclerosis: A case report

Marina Herwerth, Benedikt J Schwaiger, Kornelia Kreiser [...]

Multiple Sclerosis Journal

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Other

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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Other

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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Other

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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Other

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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Other

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

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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