4-phenylbutyric acid and arginine

4-phenylbutyric acid has been researched along with arginine in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's6 (75.00)24.3611
2020's2 (25.00)2.80

Authors

AuthorsStudies
Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K1
Erez, A; Lee, B; Nagamani, SC1
Albuquerque, JA; Castiblanco-Valencia, MM; Dos Santos, M; Isaac, L; Lamers, ML1
Enokida, T; Ishiguro, T; Maruyama, T; Okamoto, Y; Otagiri, M; Seo, H; Taguchi, K; Yamasaki, K1
Finnegan, J; Giva, S; Ihidero, P; Knerr, I; Maguire, G; Monavari, A; Power, B1
Boussery, K; De Spiegeleer, B; Peeters, E; Remon, JP; Van Tongelen, I; Vanhoorne, V; Vervaet, C; Wynendaele, E1
Fukui, K; Hanai, T; Ishibashi, H; Matsufuji, M; Nakashima, M; Takashima, S; Takeshita, E; Watanabe, Y1
Ando, Y; Arisaka, O; Imataka, G; Ishii, J; Nitta, A; Takagi, Y; Yoshihara, S1

Reviews

2 review(s) available for 4-phenylbutyric acid and arginine

ArticleYear
DILIrank: the largest reference drug list ranked by the risk for developing drug-induced liver injury in humans.
    Drug discovery today, 2016, Volume: 21, Issue:4

    Topics: Chemical and Drug Induced Liver Injury; Databases, Factual; Drug Labeling; Humans; Pharmaceutical Preparations; Risk

2016
Argininosuccinate lyase deficiency.
    Genetics in medicine : official journal of the American College of Medical Genetics, 2012, Volume: 14, Issue:5

    Topics: Arginine; Argininosuccinate Lyase; Argininosuccinic Acid; Argininosuccinic Aciduria; Child, Preschool; Citrulline; Cognition Disorders; Diet, Protein-Restricted; Fumarates; Genetic Testing; Glucose; Humans; Hyperammonemia; Hypertension; Infant; Infant, Newborn; Lipids; Liver Diseases; Liver Transplantation; Neonatal Screening; Phenylbutyrates; Sodium Benzoate

2012

Other Studies

6 other study(ies) available for 4-phenylbutyric acid and arginine

ArticleYear
Chemical chaperones curcumin and 4-phenylbutyric acid improve secretion of mutant factor H R127H by fibroblasts from a factor H-deficient patient.
    Journal of immunology (Baltimore, Md. : 1950), 2012, Sep-15, Volume: 189, Issue:6

    Topics: Amino Acid Substitution; Animals; Arginine; Cells, Cultured; Child; Chlorocebus aethiops; Complement Factor H; COS Cells; Curcumin; Fibroblasts; Histidine; Humans; Molecular Chaperones; Phenylbutyrates

2012
Tyrosine411 and Arginine410 of Human Serum Albumin Play an Important Role in the Binding of Sodium 4-Phenylbutyrate to Site II.
    Journal of pharmaceutical sciences, 2016, Volume: 105, Issue:6

    Topics: Antineoplastic Agents; Arginine; Binding Sites; Humans; Phenylbutyrates; Protein Binding; Serum Albumin, Human; Tyrosine

2016
Hyperammonaemia in Neonates and Young Children: Potential Metabolic Causes, Diagnostic Approaches and Clinical Consequences
    Irish medical journal, 2019, 01-15, Volume: 112, Issue:1

    Topics: Ammonia; Arginine; Biomarkers; Brain Diseases, Metabolic, Inborn; Carnitine; Critical Illness; Diet, Protein-Restricted; Early Diagnosis; Emergencies; Female; Humans; Hyperammonemia; Infant; Infant, Newborn; Male; Phenylbutyrates; Sodium Benzoate; Treatment Outcome

2019
Pharmaceutical compounding of orphan active ingredients in Belgium: how community and hospital pharmacists can address the needs of patients with rare diseases.
    Orphanet journal of rare diseases, 2019, 08-01, Volume: 14, Issue:1

    Topics: Arginine; Belgium; Carnitine; Drug Compounding; Excipients; Humans; Pharmacists; Phenylbutyrates; Primaquine; Pyridoxal Phosphate; Rare Diseases; Sodium Benzoate

2019
Sodium phenylbutyrate improved the clinical state in an adult patient with arginase 1 deficiency.
    Brain & development, 2020, Volume: 42, Issue:2

    Topics: Adult; Arginase; Arginine; Female; Humans; Hyperammonemia; Hyperargininemia; Phenylbutyrates

2020
Long-term survival of a patient with acute neonatal-onset metabolic encephalopathy with carbamoyl phosphate synthetase 1 deficiency.
    European review for medical and pharmacological sciences, 2020, Volume: 24, Issue:19

    Topics: Arginine; Brain Diseases, Metabolic; Carbamoyl-Phosphate Synthase I Deficiency Disease; Carnitine; Female; Humans; Hyperammonemia; Infant, Newborn; Phenylbutyrates; Renal Dialysis; Sodium Benzoate

2020