Compounds > valerates
Page last updated: 2024-09-02

valerates and tiglylglycine

valerates has been researched along with tiglylglycine in 4 studies

Compound Research Comparison

Studies
(valerates)		Trials
(valerates)		Recent Studies (post-2010)
(valerates)		Studies
(tiglylglycine)		Trials
(tiglylglycine)		Recent Studies (post-2010) (tiglylglycine)
2,2512944572006

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19902 (50.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bartlett, K; Cannon, RA; Conde, C; Gomez Vazquez, J; Lipson, M; Middleton, B; Nyhan, WL; Romanos, A; Sweetman, L1
Draffan, GH; Gompertz, D1
Baldellou, A; Briones, P; Campistol, J; Cortés, N; Delpiccolo, C; Fernández, C; Fons, C; Fuentes-Castelló, MA; García-Villoria, J; González, I; Hernández-Gonzalez, A; Messeguer, A; Navarro-Sastre, A; Pérez-Cerdá, C; Ribes, A1
Afroze, B; Ali, ZZ; Fatimah, M; Jafri, L; Jamil, A; Khan, AH; Majid, H; Yusufzai, N1

Other Studies

4 other study(ies) available for valerates and tiglylglycine

ArticleYear
3-Ketothiolase deficiency.
    European journal of pediatrics, 1986, Volume: 144, Issue:6

    Topics: 3-Hydroxybutyric Acid; Acetyl Coenzyme A; Acetyl-CoA C-Acyltransferase; Acyl Coenzyme A; Acyltransferases; Child; Female; Fibroblasts; Glycine; Humans; Hydroxybutyrates; Infant; Isoleucine; Ketosis; Male; Valerates

1986
The identification of tiglylglycine in the urine of a child with -methylcrotonylglycinuria.
    Clinica chimica acta; international journal of clinical chemistry, 1972, Volume: 37

    Topics: Amino Acid Metabolism, Inborn Errors; Butyrates; Child; Chromatography, Gas; Chromatography, Thin Layer; Coenzyme A; Diet Therapy; Dietary Proteins; Glycine; Humans; Hydro-Lyases; Male; Mass Spectrometry; Valerates

1972
Study of patients and carriers with 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: difficulties in the diagnosis.
    Clinical biochemistry, 2009, Volume: 42, Issue:1-2

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; Alcohol Oxidoreductases; Amino Acid Metabolism, Inborn Errors; Female; Glycine; Heredodegenerative Disorders, Nervous System; Humans; Hydroxybutyrates; Infant; Infant, Newborn; Male; Valerates

2009
Diagnostic dilemma of patients with methylmalonic aciduria: Experience from a tertiary care centre in Pakistan.
    JPMA. The Journal of the Pakistan Medical Association, 2018, Volume: 68, Issue:4

    Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Citrates; Cross-Sectional Studies; Female; Glycine; Humans; Infant; Lactic Acid; Male; Methionine; Mitochondrial Diseases; Pakistan; Tertiary Care Centers; Urinalysis; Valerates; Vitamin B 12 Deficiency

2018