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pteridines and Abnormalities, Multiple

pteridines has been researched along with Abnormalities, Multiple in 2 studies

Abnormalities, Multiple: Congenital abnormalities that affect more than one organ or body structure.

Research Excerpts

ExcerptRelevanceReference
"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."1.27Report 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)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Seidahmed, MZ1
Alyamani, EA1
Rashed, MS1
Saadallah, AA1
Abdelbasit, OB1
Shaheed, MM1
Rasheed, A1
Hamid, FA1
Sabry, MA1
Endres, W1
Shin, YS1
Günther, R1
Ibel, H1
Duran, M1
Wadman, SK1

Other Studies

2 other studies available for pteridines and Abnormalities, Multiple

ArticleYear
Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiency.
    American journal of medical genetics. Part A, 2005, Jul-15, Volume: 136, Issue:2

    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.
    European journal of pediatrics, 1988, Volume: 148, Issue:3

    Topics: Abnormalities, Multiple; Coenzymes; Humans; Infant; Ketone Oxidoreductases; Male; Metalloproteins; M

1988