4-methylumbelliferyl-galactopyranoside and Leukodystrophy, Globoid Cell

4-methylumbelliferyl-galactopyranoside has been researched along with Leukodystrophy, Globoid Cell in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Kolodny, EH; Krivit, W; Kurtzberg, J; Pastores, GM; Raghavan, S; Torres, PA; Zeng, B	1

Other Studies

1 other study(ies) available for 4-methylumbelliferyl-galactopyranoside and Leukodystrophy, Globoid Cell

Article	Year
Globoid cell leukodystrophy (Krabbe disease): normal umbilical cord blood galactocerebrosidase activity and polymorphic mutations. Journal of inherited metabolic disease, 2005, Volume: 28, Issue:6 Topics: Alleles; Central Nervous System; Cryopreservation; DNA, Complementary; Fetal Blood; Galactosides; Galactosylceramidase; Hematopoietic Stem Cell Transplantation; Heterozygote; HLA Antigens; Homozygote; Humans; Hymecromone; Leukodystrophy, Globoid Cell; Lysosomes; Mutation; Polymorphism, Genetic	2005

Article

Year

Globoid cell leukodystrophy (Krabbe disease): normal umbilical cord blood galactocerebrosidase activity and polymorphic mutations.

Journal of inherited metabolic disease, 2005, Volume: 28, Issue:6

Topics: Alleles; Central Nervous System; Cryopreservation; DNA, Complementary; Fetal Blood; Galactosides; Galactosylceramidase; Hematopoietic Stem Cell Transplantation; Heterozygote; HLA Antigens; Homozygote; Humans; Hymecromone; Leukodystrophy, Globoid Cell; Lysosomes; Mutation; Polymorphism, Genetic

2005