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E Wassmer

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Molecular Genetics and Metabolism|October 1, 2011

Promoter mutation is a common variant in GJC2-associated Pelizaeus-Merzbacher-like diseaseE Meyer, M A Kurian, N V Morgan, et al.

European Journal of Neurology|February 15, 2018

Paediatric acute disseminated encephalomyelitis followed by optic neuritis: disease course, treatment response and outcomeY Y M Wong, Y Hacohen, T Armangue, et al.

Neurology|April 30, 2008

Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN)M A Kurian, N V Morgan, L MacPherson, et al.

Neurology|October 27, 2010

Genotype-phenotype correlation in vanishing white matter diseaseH D W van der Lei, C G M van Berkel, W N van Wieringen, et al.

Pageof 3

Search research articles

Showing results (21-30 of 24) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 24 results.

Molecular Genetics and Metabolism|October 1, 2011

Promoter mutation is a common variant in GJC2-associated Pelizaeus-Merzbacher-like diseaseE Meyer, M A Kurian, N V Morgan, et al.

European Journal of Neurology|February 15, 2018

Paediatric acute disseminated encephalomyelitis followed by optic neuritis: disease course, treatment response and outcomeY Y M Wong, Y Hacohen, T Armangue, et al.

Neurology|April 30, 2008

Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN)M A Kurian, N V Morgan, L MacPherson, et al.

Neurology|October 27, 2010

Genotype-phenotype correlation in vanishing white matter diseaseH D W van der Lei, C G M van Berkel, W N van Wieringen, et al.

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