Page last updated: 2024-10-28

ibudilast and Leukodystrophy, Globoid Cell

ibudilast has been researched along with Leukodystrophy, Globoid Cell in 1 studies

Leukodystrophy, Globoid Cell: An autosomal recessive metabolic disorder caused by a deficiency of GALACTOSYLCERAMIDASE leading to intralysosomal accumulation of galactolipids such as GALACTOSYLCERAMIDES and PSYCHOSINE. It is characterized by demyelination associated with large multinucleated globoid cells, predominantly involving the white matter of the central nervous system. The loss of MYELIN disrupts normal conduction of nerve impulses.

Research Excerpts

ExcerptRelevanceReference
"Krabbe disease (globoid cell leukodystrophy, GLD) is an inherited disease caused by a deficiency in the lysosomal enzyme galactocerebrosidase (GALC)."2.53Insights into the Pathogenesis and Treatment of Krabbe Disease. ( Bongarzone, ER; Escolar, ML; Gray, SJ; Kafri, T; Sands, MS; Vite, CH, 2016)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bongarzone, ER1
Escolar, ML1
Gray, SJ1
Kafri, T1
Vite, CH1
Sands, MS1

Reviews

1 review available for ibudilast and Leukodystrophy, Globoid Cell

ArticleYear
Insights into the Pathogenesis and Treatment of Krabbe Disease.
    Pediatric endocrinology reviews : PER, 2016, Volume: 13 Suppl 1

    Topics: Acetylcysteine; Animals; Antimetabolites; Bone Marrow Transplantation; Central Nervous System; Cyclo

2016