Page last updated: 2024-10-20

urea and Galactosemias

urea has been researched along with Galactosemias in 7 studies

pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.

Galactosemias: A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19906 (85.71)18.7374
1990's1 (14.29)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mowat, AP1
Henderson, JM1
Warren, WD1
Snyderman, SE1
Kirschbaum, BB1
Omenn, GS1
Heindorff, H1
Almdal, T1
Vilstrup, H1
O'Reilly, S1

Reviews

4 reviews available for urea and Galactosemias

ArticleYear
Hepatic Disorders.
    Clinics in gastroenterology, 1982, Volume: 11, Issue:1

    Topics: Adolescent; Adult; alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Ammonia; Ch

1982
Selective variceal decompression: current status and recent advances.
    Advances in surgery, 1984, Volume: 18

    Topics: Amino Acids; Ammonia; Angiography; Ascites; Brain Diseases; Esophageal and Gastric Varices; Galactos

1984
The dietary therapy of inherited metabolic disease.
    Progress in food & nutrition science, 1975, Volume: 1, Issue:7-8

    Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Child; C

1975
Inborn errors of metabolism: clues to understanding human behavioral disorders.
    Behavior genetics, 1976, Volume: 6, Issue:3

    Topics: Adrenal Hyperplasia, Congenital; Brain; Galactosemias; Glycine; Hepatolenticular Degeneration; Heter

1976

Other Studies

3 other studies available for urea and Galactosemias

ArticleYear
Glycoprotein metabolism in human renal disease: serum glycoproteins and glycoprotein: glycosyl transferase levels in chronic renal failure.
    The Journal of laboratory and clinical medicine, 1975, Volume: 86, Issue:5

    Topics: ABO Blood-Group System; Adolescent; Adult; beta-N-Acetylglucosaminylglycopeptide beta-1,4-Galactosyl

1975
Contradictory effects of uncomplicated versus complicated abdominal surgery on the hepatic capacity for urea synthesis in rats.
    The Journal of surgical research, 1990, Volume: 49, Issue:3

    Topics: Amino Acids; Animals; Blood Glucose; Eating; Female; Galactosemias; Glucagon; Hysterectomy; Insulin;

1990
Neurologic disorders and liver disease.
    Postgraduate medicine, 1971, Volume: 50, Issue:3

    Topics: Adipose Tissue; Ammonia; Brain Diseases; Citrulline; Fatty Liver; Galactosemias; Hepatic Encephalopa

1971