Page last updated: 2024-11-02

phenylbutazone and Deficiency Disease, Ornithine Carbamoyltransferase

phenylbutazone has been researched along with Deficiency Disease, Ornithine Carbamoyltransferase in 3 studies

Phenylbutazone: A butyl-diphenyl-pyrazolidinedione that has anti-inflammatory, antipyretic, and analgesic activities. It has been used in ANKYLOSING SPONDYLITIS; RHEUMATOID ARTHRITIS; and REACTIVE ARTHRITIS.
phenylbutazone : A member of the class of pyrazolidines that is 1,2-diphenylpyrazolidine-3,5-dione carrying a butyl group at the 4-position.

Research Excerpts

ExcerptRelevanceReference
"Ornithine transcarbamylase deficiency is the most common inherited urea cycle disorder."6.43[Hyperammonemia type II as an example of urea cycle disorder]. ( Duława, J; Hawrot-Kawecka, AM; Kawecki, GP, 2006)
"Ornithine transcarbamylase deficiency is the most common inherited urea cycle disorder."2.43[Hyperammonemia type II as an example of urea cycle disorder]. ( Duława, J; Hawrot-Kawecka, AM; Kawecki, GP, 2006)
"The symptoms and signs of ornithine transcarbamylase deficiency are discussed."2.42Ornithine transcarbamylase deficiency: a urea cycle defect. ( Gordon, N, 2003)
"X-linked inherited ornithine transcarbamylase deficiency is the most frequent urea cycle disorder."1.31Late diagnosis of ornithine transcarbamylase defect in three related female patients: polymorphic presentations. ( Garrigue, MA; Kouatchet, A; Labarthe, F; Legras, A; Maillot, F; Ogier de Baulny, H, 2002)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gordon, N1
Hawrot-Kawecka, AM1
Kawecki, GP1
Duława, J1
Legras, A1
Labarthe, F1
Maillot, F1
Garrigue, MA1
Kouatchet, A1
Ogier de Baulny, H1

Reviews

2 reviews available for phenylbutazone and Deficiency Disease, Ornithine Carbamoyltransferase

ArticleYear
Ornithine transcarbamylase deficiency: a urea cycle defect.
    European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2003, Volume: 7, Issue:3

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Food Preservatives; Humans; Hyperammonemia; Infant, Newborn

2003
[Hyperammonemia type II as an example of urea cycle disorder].
    Wiadomosci lekarskie (Warsaw, Poland : 1960), 2006, Volume: 59, Issue:7-8

    Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Coma; Female; Humans; Hyperammonemi

2006

Other Studies

1 other study available for phenylbutazone and Deficiency Disease, Ornithine Carbamoyltransferase

ArticleYear
Late diagnosis of ornithine transcarbamylase defect in three related female patients: polymorphic presentations.
    Critical care medicine, 2002, Volume: 30, Issue:1

    Topics: Adult; Coma; Female; Hemofiltration; Humans; Hyperammonemia; Middle Aged; Ornithine Carbamoyltransfe

2002