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Clinical findings in Pelizaeus-Merzbacher disease
Meredith R. Golomb
, Laurence E. Walsh
,
Karen S. Carvalho
, Celanie K. Christensen
, William E. DeMyer
Indiana University Bloomington
Riley Hospital for Children
Research output
:
Contribution to journal
›
Article
›
peer-review
25
Scopus citations
Overview
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Medicine and Dentistry
Clinical Finding
100%
Synapsin I
100%
Pelizaeus Merzbacher Disease
100%
Proteolipid Protein
100%
Spasticity
33%
Arm
33%
Stereotypic Movement Disorder
33%
Disease Course
33%
Central Nervous System
33%
Meconium Aspiration Syndrome
33%
Myelination
33%
Hypotonia
33%
X Chromosome Linked Disorder
33%
Point Mutation
33%
Speech Production
33%
Ataxia
33%
Gestational Hypertension
33%
Codon
33%
Newborn Disease
33%
Gene Duplication
33%
Nystagmus
33%
Neuroscience
Proteolipid Protein 1
100%
Central Nervous System
33%
Hypertension
33%
Hypotonia
33%
Myelinogenesis
33%
Codon
33%
Nystagmus
33%
Point Mutation
33%
Stereotypic Movement Disorder
33%
Ataxia
33%
Gene Duplication
33%
Biochemistry, Genetics and Molecular Biology
Pelizaeus-Merzbacher Disease
100%
Proteolipid Protein 1
100%
Gene Duplication
33%
Genotyping
33%
Point Mutation
33%
Myelination
33%
Codon
33%