pteridines has been researched along with Abnormalities, Multiple in 2 studies
Abnormalities, Multiple: Congenital abnormalities that affect more than one organ or body structure.
Excerpt | Relevance | Reference |
---|---|---|
"A newborn infant exhibiting seizures and spastic tetraparesis at the age of 1 week was shown to excrete excessive quantities of sulphite, taurine, S-sulphocysteine and thiosulphate, characteristic of sulphite oxidase deficiency." | 1.27 | Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiency. ( Duran, M; Endres, W; Günther, R; Ibel, H; Shin, YS; Wadman, SK, 1988) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (50.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Seidahmed, MZ | 1 |
Alyamani, EA | 1 |
Rashed, MS | 1 |
Saadallah, AA | 1 |
Abdelbasit, OB | 1 |
Shaheed, MM | 1 |
Rasheed, A | 1 |
Hamid, FA | 1 |
Sabry, MA | 1 |
Endres, W | 1 |
Shin, YS | 1 |
Günther, R | 1 |
Ibel, H | 1 |
Duran, M | 1 |
Wadman, SK | 1 |
2 other studies available for pteridines and Abnormalities, Multiple
Article | Year |
---|---|
Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiency.
Topics: Abnormalities, Multiple; Arabs; Base Sequence; Binding Sites; Coenzymes; Consanguinity; Dimerization | 2005 |
Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiency.
Topics: Abnormalities, Multiple; Coenzymes; Humans; Infant; Ketone Oxidoreductases; Male; Metalloproteins; M | 1988 |