Distinct progression patterns of brain disease in infantile and juvenile gangliosidoses: Volumetric quantitative MRI study

BACKGROUND: GM1-gangliosidosis and GM2-gangliosidosis (Tay-Sachs disease and Sandhoff disease) are unrelenting heritable neurodegenerative conditions of lysosomal ganglioside accumulation. Although progressive brain atrophy is characteristic, longitudinal quantification of specific brain structures...

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Bibliografiska uppgifter
I publikationen:Mol Genet Metab
Huvudupphovsmän: Nestrasil, Igor, Ahmed, Alia, Utz, Josephine M., Rudser, Kyle, Whitley, Chester B., Jarnes-Utz, Jeanine R.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2017
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5832355/
https://ncbi.nlm.nih.gov/pubmed/29352662
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2017.12.432
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