ouabain and Gargoylism, Hunter Syndrome

ouabain has been researched along with Gargoylism, Hunter Syndrome 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
Bonnet, V; Bozon, D; Cudry, S; Froissart, R; Maire, I; Tigaud, I	1

Other Studies

1 other study(ies) available for ouabain and Gargoylism, Hunter Syndrome

Article	Year
MPS II in females: molecular basis of two different cases. Journal of medical genetics, 2000, Volume: 37, Issue:10 Topics: Alleles; Animals; Blotting, Southern; Cell Line; Child; Child, Preschool; Chromosome Deletion; DNA Methylation; Dosage Compensation, Genetic; Fatal Outcome; Female; Fibroblasts; France; Genes, Recessive; Humans; Hybrid Cells; Iduronate Sulfatase; In Situ Hybridization, Fluorescence; Introns; Male; Mucopolysaccharidosis II; Mutation; Ouabain; Phenotype; Polymorphism, Genetic; RNA, Messenger; X Chromosome	2000

Article

Year

MPS II in females: molecular basis of two different cases.

Journal of medical genetics, 2000, Volume: 37, Issue:10

Topics: Alleles; Animals; Blotting, Southern; Cell Line; Child; Child, Preschool; Chromosome Deletion; DNA Methylation; Dosage Compensation, Genetic; Fatal Outcome; Female; Fibroblasts; France; Genes, Recessive; Humans; Hybrid Cells; Iduronate Sulfatase; In Situ Hybridization, Fluorescence; Introns; Male; Mucopolysaccharidosis II; Mutation; Ouabain; Phenotype; Polymorphism, Genetic; RNA, Messenger; X Chromosome

2000