Compounds > pyrroles
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pyrroles and Metabolism, Inborn Errors

pyrroles has been researched along with Metabolism, Inborn Errors in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19904 (66.67)18.7374
1990's0 (0.00)18.2507
2000's1 (16.67)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mills, GA; Walker, V1
Baumer, A; Baumgartner, M; Bozorgmehr, B; Giunta, C; Häberle, J; Hausser, I; Kariminejad, A; Kariminejad, MH; Kretz, R; Rohrbach, M1
Compernolle, F; De Groote, J; Desmet, V; Fevery, J; Heirwegh, KP; Meuwissen, JA; Van Roy, FP1
Coleman, DL; Levin, EY; Russell, ES1
Chatterjea, JB; Chatterji, AK1
Marosvári, I; Miltényi, M1

Other Studies

6 other study(ies) available for pyrroles and Metabolism, Inborn Errors

ArticleYear
N-(pyrrole-2-carboxyl) glycine a diagnostic marker of hyperprolinaemia type II: mass spectra of trimethylsilyl derivatives.
    Clinica chimica acta; international journal of clinical chemistry, 2009, Volume: 405, Issue:1-2

    Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Biomarkers; Child; Glycine; Humans; Hydroxyproline; Mass Spectrometry; Metabolism, Inborn Errors; Proline; Pyrroles; Trimethylsilyl Compounds

2009
Defect in proline synthesis: pyrroline-5-carboxylate reductase 1 deficiency leads to a complex clinical phenotype with collagen and elastin abnormalities.
    Journal of inherited metabolic disease, 2011, Volume: 34, Issue:3

    Topics: Abnormalities, Multiple; Adolescent; Adult; Child; Child, Preschool; Collagen; delta-1-Pyrroline-5-Carboxylate Reductase; DNA Mutational Analysis; Elastin; Family; Female; Humans; Infant; Male; Metabolism, Inborn Errors; Middle Aged; Models, Biological; Mutation, Missense; Phenotype; Proline; Pyrroles; Pyrroline Carboxylate Reductases; Young Adult

2011
Recent advances in the separation and analysis of diazo-positive bile pigments.
    Methods of biochemical analysis, 1974, Volume: 22

    Topics: Amniotic Fluid; Azo Compounds; Bile Pigments; Bilirubin; Chromatography, Thin Layer; Drug Stability; Female; Hexosyltransferases; Histocytochemistry; Humans; Hyperbilirubinemia; Hyperbilirubinemia, Hereditary; Indicators and Reagents; Mathematics; Metabolism, Inborn Errors; Pregnancy; Pyrroles; Solubility; Sulfur Radioisotopes; Uridine Diphosphate Sugars

1974
Enzymatic studies of the hemopoietic defect in flexed mice.
    Genetics, 1969, Volume: 61, Issue:3

    Topics: Anemia, Sideroblastic; Animals; Animals, Newborn; Bone Marrow; Chromosome Mapping; Erythropoiesis; Female; Fetal Diseases; Genes; Genetic Linkage; Hydro-Lyases; Iron; Levulinic Acids; Liver; Lyases; Metabolism, Inborn Errors; Mice; Phenylhydrazines; Pregnancy; Propionates; Pyrroles; Spleen

1969
Porphyrins and porphyrias: new horizons.
    Bulletin of the Calcutta School of Tropical Medicine, 1969, Volume: 17, Issue:3

    Topics: Anemia, Sideroblastic; Heme; India; Metabolic Diseases; Metabolism, Inborn Errors; Porphyrias; Porphyrins; Pyrroles

1969
Congenital haemolytic anaemia associated with haemoglobin anomaly and mesobilifuscinuria.
    Acta paediatrica Academiae Scientiarum Hungaricae, 1968, Volume: 9, Issue:3

    Topics: Anemia, Hemolytic, Congenital; Child; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Male; Metabolism, Inborn Errors; Porphyrins; Pyrroles

1968