Page last updated: 2024-08-16

succinylacetone and nitisinone

succinylacetone has been researched along with nitisinone in 16 studies

Research

Studies (16)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (18.75)18.2507
2000's1 (6.25)29.6817
2010's11 (68.75)24.3611
2020's1 (6.25)2.80

Authors

AuthorsStudies
Hjalmarson, O; Holme, E; Lindstedt, S; Lock, EA; Strandvik, B1
al-Dhalimy, M; Finegold, M; Grompe, M; Kennaway, NG; Lindstedt, S; Ou, CN; Papaconstantinou, J; Torres-Ramos, CA1
Barkaoui, E; Bernard, O; Debray, D; Habès, D; Ogier, H1
Al Amoudi, M; Al-Ahaidib, LY; Al-Dbaas, A; Al-Dirbashi, OY; Al-Hassnan, Z; Al-Owain, M; Al-Sayed, MM; Ni Luanaigh, M; Rahbeeni, Z; Rashed, MS1
Al-Dirbashi, O; El-Hawary, M; El-Karaksy, H; El-Koofy, N; El-Raziky, M; El-Sayed, R; Rashed, M1
Boenzi, S; Della Bona, ML; Dionisi-Vici, C; la Marca, G; Malvagia, S; Martinelli, D; Materazzi, S1
Herebian, D; Schlune, A; Spiekerkoetter, U; Thimm, E1
Bartlett, DC; Holme, E; Lloyd, C; McKiernan, PJ; Newsome, PN; Preece, MA1
Benoist, JF; Davit-Spraul, A; Garcia Segarra, N; Grenèche, MO; Imbard, A; Ogier de Baulny, H; Roche, S1
Al Jurayyan, NA; Al-Jarallah, AS; Al-Nemri, A; Babiker, A; Hasanato, R; Kambal, MA; Mohamed, S1
Peake, RW1
Mannion, MA; Mayne, P; Monavari, AA; Smith, A1
Alvarez, F; Atkinson, S; Bouchard, M; Brunel-Guitton, C; Buhas, D; Bussières, JF; Dubois, J; Fenyves, D; Goodyer, P; Gosselin, M; Halac, U; Labbé, P; Laframboise, R; Maranda, B; Melançon, S; Merouani, A; Mitchell, GA; Mitchell, J; Parizeault, G; Pelletier, L; Phan, V; Turcotte, JF1
Christensen, M; Lund, AM; Sundberg, J; Wibrand, F1
Burgerhof, JGM; Daly, A; de Blaauw, P; Heiner-Fokkema, MR; Kienstra, NS; MacDonald, A; Rodenburg, IL; Santra, S; van de Krogt, J; van Ginkel, WG; van Reemst, HE; van Spronsen, FJ1
Gavrilov, DK; Matern, D; Netzel, BC; Oglesbee, D; Pino, GB; Raymond, KM; Rinaldo, P; Schultz, MJ; Singh, RH; Smith, WE; Tortorelli, S1

Reviews

1 review(s) available for succinylacetone and nitisinone

ArticleYear
The Québec NTBC Study.
    Advances in experimental medicine and biology, 2017, Volume: 959

    Topics: Cyclohexanones; Enzyme Inhibitors; Heptanoates; Humans; Infant, Newborn; Liver Diseases; Liver Transplantation; Neonatal Screening; Nitrobenzoates; Quebec; Tyrosinemias

2017

Other Studies

15 other study(ies) available for succinylacetone and nitisinone

ArticleYear
Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase.
    Lancet (London, England), 1992, Oct-03, Volume: 340, Issue:8823

    Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Acetoacetates; alpha-Fetoproteins; Amino Acid Metabolism, Inborn Errors; Aminolevulinic Acid; Child; Child, Preschool; Cyclohexanones; Erythrocytes; Heptanoates; Humans; Hydroxybenzoates; Infant; Kidney Tubules; Liver; Nitrobenzoates; Phenylalanine; Phosphates; Porphobilinogen Synthase; Proteinuria; Tyrosine

1992
Pharmacological correction of neonatal lethal hepatic dysfunction in a murine model of hereditary tyrosinaemia type I.
    Nature genetics, 1995, Volume: 10, Issue:4

    Topics: alpha-Fetoproteins; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Cyclohexanones; Disease Models, Animal; Enzyme Inhibitors; Female; Heptanoates; Humans; Hydrolases; Liver; Liver Diseases; Liver Neoplasms; Male; Mice; Mice, Inbred C57BL; Nitrobenzoates; Pancreas; RNA, Messenger; Tyrosine

1995
[Favorable outcome of treatment with NTBC of acute liver insufficiency disclosing hereditary tyrosinemia type I].
    Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 1999, Volume: 6, Issue:5

    Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Acute Disease; Amino Acid Metabolism, Inborn Errors; Aminolevulinic Acid; Cyclohexanones; Enzyme Inhibitors; Female; Follow-Up Studies; Heptanoates; Humans; Infant; Infant, Newborn; Liver Failure; Male; Methionine; Nitrobenzoates; Porphobilinogen Synthase; Treatment Outcome; Tyrosine

1999
Tandem mass spectrometric assay of succinylacetone in urine for the diagnosis of hepatorenal tyrosinemia.
    Analytical biochemistry, 2005, Apr-15, Volume: 339, Issue:2

    Topics: Adolescent; Adult; Child; Child, Preschool; Cyclohexanones; Enzyme Inhibitors; Heptanoates; Humans; Infant; Infant, Newborn; Mass Spectrometry; Middle Aged; Neonatal Screening; Nitrobenzoates; Reproducibility of Results; Tyrosinemias

2005
Clinical practice. NTBC therapy for tyrosinemia type 1: how much is enough?
    European journal of pediatrics, 2010, Volume: 169, Issue:6

    Topics: Child, Preschool; Cost-Benefit Analysis; Cyclohexanones; Dose-Response Relationship, Drug; Drug Costs; Egypt; Enzyme Inhibitors; Female; Heptanoates; Humans; Infant; Nitrobenzoates; Tyrosinemias

2010
LC-MS/MS method for simultaneous determination on a dried blood spot of multiple analytes relevant for treatment monitoring in patients with tyrosinemia type I.
    Analytical chemistry, 2012, Jan-17, Volume: 84, Issue:2

    Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Adolescent; Biomarkers; Child; Child, Preschool; Chromatography, Liquid; Cyclohexanones; Diet, Protein-Restricted; Drug Monitoring; Enzyme Inhibitors; Heptanoates; Humans; Infant; Infant, Newborn; Kidney; Liver; Methionine; Nitrobenzoates; Phenylalanine; Tandem Mass Spectrometry; Tyrosine; Tyrosinemias

2012
Single dose NTBC-treatment of hereditary tyrosinemia type I.
    Journal of inherited metabolic disease, 2012, Volume: 35, Issue:5

    Topics: Cyclohexanones; Drug Administration Schedule; Female; Heptanoates; Humans; Infant; Infant, Newborn; Male; Nitrobenzoates; Tyrosinemias

2012
Plasma succinylacetone is persistently raised after liver transplantation in tyrosinaemia type 1.
    Journal of inherited metabolic disease, 2013, Volume: 36, Issue:1

    Topics: Adolescent; Child; Child, Preschool; Cyclohexanones; Heptanoates; Humans; Infant; Liver Transplantation; Nitrobenzoates; Porphobilinogen Synthase; Retrospective Studies; Tyrosinemias

2013
Maternal and fetal tyrosinemia type I.
    Journal of inherited metabolic disease, 2010, Volume: 33 Suppl 3

    Topics: Biomarkers; Child Development; Consanguinity; Cyclohexanones; Diet, Protein-Restricted; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Heptanoates; Heredity; Heterozygote; Homozygote; Humans; Hydrolases; Infant; Infant, Newborn; Live Birth; Mutation; Nitrobenzoates; Pedigree; Phenotype; Pregnancy; Tyrosine; Tyrosinemias; Young Adult

2010
Tyrosinemia type 1: a rare and forgotten cause of reversible hypertrophic cardiomyopathy in infancy.
    BMC research notes, 2013, Sep-09, Volume: 6

    Topics: Cardiomyopathy, Hypertrophic; Cyclohexanones; Food, Formulated; Heptanoates; Homozygote; Humans; Hydrolases; Infant; Male; Mutation; Nitrobenzoates; Siblings; Treatment Outcome; Tyrosinemias

2013
Deranged Liver Function in a Neonate.
    Clinical chemistry, 2016, Volume: 62, Issue:11

    Topics: Biomarkers; Cyclohexanones; Enzyme Inhibitors; Female; Gas Chromatography-Mass Spectrometry; Heptanoates; Humans; Infant, Newborn; Liver Diseases; Neonatal Screening; Nitrobenzoates; Tyrosinemias; Urinalysis

2016
Type 1 Tyrosinaemia.
    Irish medical journal, 2016, Jun-10, Volume: 109, Issue:6

    Topics: Biomarkers; Cyclohexanones; Enzyme Inhibitors; Heptanoates; Humans; Hydrolases; Hypoglycemia; Ireland; Liver Transplantation; Mutation; Nitrobenzoates; Tyrosinemias

2016
Simultaneous quantification of succinylacetone and nitisinone for therapeutic drug monitoring in the treatment of Tyrosinemia type 1.
    Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2018, Jan-01, Volume: 1072

    Topics: Chromatography, Liquid; Cyclohexanones; Drug Monitoring; Heptanoates; Humans; Linear Models; Nitrobenzoates; Reproducibility of Results; Sensitivity and Specificity; Tandem Mass Spectrometry; Tyrosinemias

2018
The Effect of Various Doses of Phenylalanine Supplementation on Blood Phenylalanine and Tyrosine Concentrations in Tyrosinemia Type 1 Patients.
    Nutrients, 2019, Nov-18, Volume: 11, Issue:11

    Topics: Adolescent; Adult; Child; Cyclohexanones; Dietary Supplements; Enzyme Inhibitors; Female; Heptanoates; Humans; Linear Models; Male; Nitrobenzoates; Phenylalanine; Tyrosine; Tyrosinemias; Young Adult

2019
Laboratory monitoring of patients with hereditary tyrosinemia type I.
    Molecular genetics and metabolism, 2020, Volume: 130, Issue:4

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acids; Biomarkers; Case-Control Studies; Child; Child, Preschool; Cyclohexanones; Female; Follow-Up Studies; Heptanoates; Humans; Infant; Infant, Newborn; Laboratories; Male; Middle Aged; Nitrobenzoates; Prognosis; Reference Standards; Specimen Handling; Tyrosinemias; Young Adult

2020