Page last updated: 2024-10-20

thymine and Dihydropyrimidine Dehydrogenase Deficiency

thymine has been researched along with Dihydropyrimidine Dehydrogenase Deficiency in 10 studies

Dihydropyrimidine Dehydrogenase Deficiency: An autosomal recessive disorder affecting DIHYDROPYRIMIDINE DEHYDROGENASE and causing familial pyrimidinemia. It is characterized by thymine-uraciluria in homozygous deficient patients. Even a partial deficiency in the enzyme leaves individuals at risk for developing severe 5-FLUOROURACIL-associated toxicity.

Research Excerpts

ExcerptRelevanceReference
"Thus, DPD deficiency may feature prominent brain abnormalities involving the cerebral white matter and brainstem."1.32Head imaging abnormalities in dihydropyrimidine dehydrogenase deficiency. ( Barkovich, AJ; Enns, GM; Manning, M; Sanger, T; van Gennip, AH; van Kuilenburg, AB; Witt, DR, 2004)
"In addition to this study we analyzed a DPD deficiency case and a DHPuria case."1.30Possible prediction of adverse reactions to fluorouracil by the measurement of urinary dihydrothymine and thymine. ( Dobashi, K; Hayashi, K; Kidouchi, K; Kondou, M; Kouwaki, M; Sumi, S; Togari, H; Wada, Y, 1998)

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (10.00)18.2507
2000's4 (40.00)29.6817
2010's3 (30.00)24.3611
2020's2 (20.00)2.80

Authors

AuthorsStudies
Schouten, JF1
Willems, J1
Sanders, SJWJ1
Creemers, GJ1
Deenen, MJ1
Liu, N1
Sun, Q1
Bolzacchini, E1
Luchena, G1
Giordano, M1
Milano, G1
Weidensee, S1
Goettig, P1
Bertone, M1
Haas, D1
Magdolen, V1
Kiechle, M1
Meindl, A1
van Kuilenburg, AB4
Gross, E1
Stroomer, AE1
Van Lenthe, H1
Abeling, NG1
Van Gennip, AH3
Enns, GM1
Barkovich, AJ1
Manning, M1
Sanger, T1
Witt, DR1
Al-Sanna'a, NA1
Atrak, TM1
Abdul-Jabbar, MA1
Schmidt, C1
Hofmann, U1
Kohlmüller, D1
Mürdter, T1
Zanger, UM1
Schwab, M1
Hoffmann, GF1
Sumi, S1
Kidouchi, K1
Kondou, M1
Hayashi, K1
Dobashi, K1
Kouwaki, M1
Togari, H1
Wada, Y1

Other Studies

10 other studies available for thymine and Dihydropyrimidine Dehydrogenase Deficiency

ArticleYear
Standard-Dose Trifluridine/Tipiracil as Safe Treatment Alternative in Metastatic Colorectal Cancer Patients With DPD Deficiency.
    Clinical colorectal cancer, 2021, Volume: 20, Issue:4

    Topics: Colonic Neoplasms; Dihydropyrimidine Dehydrogenase Deficiency; Humans; Pyrrolidines; Rectal Neoplasm

2021
Quantitation of Pyrimidine in Urine by Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry.
    Methods in molecular biology (Clifton, N.J.), 2022, Volume: 2546

    Topics: Biomarkers; Chromatography, Liquid; Dihydropyrimidine Dehydrogenase Deficiency; Humans; Pyrimidines;

2022
Safety Report of TAS-102 in a Patient With Reduced DPD Activity.
    Clinical colorectal cancer, 2019, Volume: 18, Issue:4

    Topics: Aged; Antineoplastic Agents; Dihydropyrimidine Dehydrogenase Deficiency; Dihydrouracil Dehydrogenase

2019
Fluoropyrimidines and DPD testing: is there truly an inexorable link?
    European journal of cancer (Oxford, England : 1990), 2019, Volume: 113

    Topics: Antineoplastic Agents; Dihydropyrimidine Dehydrogenase Deficiency; Dihydrouracil Dehydrogenase (NADP

2019
A mild phenotype of dihydropyrimidine dehydrogenase deficiency and developmental retardation associated with a missense mutation affecting cofactor binding.
    Clinical biochemistry, 2011, Volume: 44, Issue:8-9

    Topics: Amino Acid Sequence; Child; Creatinine; Dihydropyrimidine Dehydrogenase Deficiency; Dihydrouracil De

2011
New insights in dihydropyrimidine dehydrogenase deficiency: a pivotal role for beta-aminoisobutyric acid?
    The Biochemical journal, 2004, Apr-01, Volume: 379, Issue:Pt 1

    Topics: Aminoisobutyric Acids; beta-Alanine; Brain Diseases, Metabolic, Inborn; Dihydropyrimidine Dehydrogen

2004
Head imaging abnormalities in dihydropyrimidine dehydrogenase deficiency.
    Journal of inherited metabolic disease, 2004, Volume: 27, Issue:4

    Topics: Brain; Dihydropyrimidine Dehydrogenase Deficiency; Fatal Outcome; Female; Humans; Infant; Magnetic R

2004
Dihydropyrimidine dehydrogenase deficiency presenting at birth.
    Journal of inherited metabolic disease, 2005, Volume: 28, Issue:5

    Topics: Age of Onset; Antimetabolites; Binding Sites; Digestive System Abnormalities; Dihydropyrimidine Dehy

2005
Comprehensive analysis of pyrimidine metabolism in 450 children with unspecific neurological symptoms using high-pressure liquid chromatography-electrospray ionization tandem mass spectrometry.
    Journal of inherited metabolic disease, 2005, Volume: 28, Issue:6

    Topics: Adolescent; beta-Alanine; Child; Child, Preschool; Chromatography, High Pressure Liquid; Dihydropyri

2005
Possible prediction of adverse reactions to fluorouracil by the measurement of urinary dihydrothymine and thymine.
    International journal of molecular medicine, 1998, Volume: 2, Issue:4

    Topics: Adolescent; Adult; Antimetabolites, Antineoplastic; Child; Child, Preschool; Dihydropyrimidine Dehyd

1998