homocysteine and Congenital Disorders of Glycosylation

homocysteine has been researched along with Congenital Disorders of Glycosylation in 1 studies

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
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, J1

Other Studies

1 other study(ies) available for homocysteine and Congenital Disorders of Glycosylation

ArticleYear
Clinical picture of S-adenosylhomocysteine hydrolase deficiency resembles phosphomannomutase 2 deficiency.
    Molecular genetics and metabolism, 2012, Volume: 107, Issue:3

    Topics: Adenosylhomocysteinase; Congenital Disorders of Glycosylation; Diagnosis, Differential; Erythrocytes; Female; Fibroblasts; Heterozygote; Homocysteine; Humans; Infant, Newborn; Methionine; Mutation; Phosphotransferases (Phosphomutases)

2012
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