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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Detalles Bibliográficos
Autores principales: Nestrasil, Igor, Ahmed, Alia, Utz, Josephine M., Rudser, Kyle, Whitley, Chester B., Jarnes-Utz, Jeanine R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832355/
https://www.ncbi.nlm.nih.gov/pubmed/29352662
http://dx.doi.org/10.1016/j.ymgme.2017.12.432

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832355/
https://www.ncbi.nlm.nih.gov/pubmed/29352662
http://dx.doi.org/10.1016/j.ymgme.2017.12.432

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