Page last updated: 2024-08-22

molybdenum and Carboxylase Deficiency, Combined

molybdenum has been researched along with Carboxylase Deficiency, Combined in 1 studies

Research

Studies (1)

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

Authors

AuthorsStudies
Bakker, HD1

Other Studies

1 other study(ies) available for molybdenum and Carboxylase Deficiency, Combined

ArticleYear
[Remember hereditary metabolic diseases in children in which no satisfactory diagnosis can be established].
    Nederlands tijdschrift voor geneeskunde, 1993, May-08, Volume: 137, Issue:19

    Topics: Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Biotinidase; Child; Child, Preschool; Coenzymes; Female; Humans; Infant, Newborn; Lysine; Male; Metabolism, Inborn Errors; Metalloproteins; Molybdenum; Molybdenum Cofactors; Multiple Carboxylase Deficiency; Pteridines

1993