homocysteine and Congenital Disorders of Glycosylation
homocysteine has been researched along with Congenital Disorders of Glycosylation 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 | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors
Authors | Studies |
---|---|
Barić, I; Bauerová, L; Belužić, R; Elleder, M; Hansíkova, H; Honzík, T; Ješina, P; Kožich, V; Krijt, J; Magner, M; Ondrušková, N; Sokolová, J; Veselá, K; Vugrek, O; Zeman, J | 1 |
Other Studies
1 other study(ies) available for homocysteine and Congenital Disorders of Glycosylation
Article | Year |
---|---|
Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 deficiency.
Topics: Adenosylhomocysteinase; Congenital Disorders of Glycosylation; Diagnosis, Differential; Erythrocytes; Female; Fibroblasts; Heterozygote; Homocysteine; Humans; Infant, Newborn; Methionine; Mutation; Phosphotransferases (Phosphomutases) | 2012 |