prednisone has been researched along with Metabolism, Inborn Errors in 16 studies
Prednisone: A synthetic anti-inflammatory glucocorticoid derived from CORTISONE. It is biologically inert and converted to PREDNISOLONE in the liver.
prednisone : A synthetic glucocorticoid drug that is particularly effective as an immunosuppressant, and affects virtually all of the immune system. Prednisone is a prodrug that is converted by the liver into prednisolone (a beta-hydroxy group instead of the oxo group at position 11), which is the active drug and also a steroid.
Metabolism, Inborn Errors: Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Cobalamin C disease is a rare genetic condition resulting in methylmalonic aciduria, homocystinuria, and hematologic abnormalities." | 3.73 | Cobalamin C disease presenting with hemophagocytic lymphohistiocytosis. ( Coates, T; Gonzalez-Gomez, I; Wu, S; Yano, S, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 12 (75.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (12.50) | 29.6817 |
| 2010's | 2 (12.50) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Wang, X | 1 |
| Chen, P | 1 |
| Sun, Y | 1 |
| Chen, Y | 1 |
| Mao, M | 1 |
| Jiang, T | 1 |
| Ouyang, J | 1 |
| Urzua, CA | 1 |
| Guerrero, J | 1 |
| Gatica, H | 1 |
| Velasquez, V | 1 |
| Goecke, A | 1 |
| BRYAN, GT | 1 |
| KLIMAN, B | 1 |
| BARTTER, FC | 1 |
| Wu, S | 1 |
| Gonzalez-Gomez, I | 1 |
| Coates, T | 1 |
| Yano, S | 1 |
| Atiq, M | 1 |
| Holt, AF | 1 |
| Safdar, K | 1 |
| Weber, F | 1 |
| Ravinuthala, R | 1 |
| Jonas, ME | 1 |
| Neff, GW | 1 |
| Riddick, DH | 1 |
| Hammond, CB | 1 |
| Starzl, TE | 1 |
| Lonchampt, F | 1 |
| Blanc, D | 1 |
| Terrasse, F | 1 |
| Humbert, P | 1 |
| Kienzler, JL | 1 |
| Agache, P | 1 |
| Gall, DG | 1 |
| Hamilton, JR | 1 |
| Rose, LI | 1 |
| Williams, GH | 1 |
| Emerson, K | 1 |
| Villee, DB | 1 |
| Teree, TM | 1 |
| Klein, LR | 1 |
| Krüger, E | 1 |
| Uhlig, J | 1 |
| Stefanini, M | 1 |
| Johnson, MA | 1 |
| Fulthorpe, JJ | 1 |
| Hudgson, P | 1 |
| Brook, CG | 1 |
| Zachmann, M | 1 |
| Prader, A | 1 |
| Mürset, G | 1 |
| Booth, CC | 1 |
1 review available for prednisone and Metabolism, Inborn Errors
| Article | Year |
|---|---|
Chronic diarrhea in childhood: a new look at an old problem.
Topics: Celiac Disease; Chlorides; Chronic Disease; Cystic Fibrosis; Diarrhea; Diet Therapy; Food Hypersensi | 1974 |
15 other studies available for prednisone and Metabolism, Inborn Errors
| Article | Year |
|---|---|
Diagnostic value of the dual-luciferase report assay for predicting response to glucocorticoid in children with acute lymphoblastic leukemia.
Topics: Adolescent; Child; Child, Preschool; Drug Resistance, Neoplasm; Female; Follow-Up Studies; Glucocort | 2017 |
Evaluation of the Glucocorticoid Receptor as a Biomarker of Treatment Response in Vogt-Koyanagi-Harada Disease.
Topics: Adult; Biomarkers; Dose-Response Relationship, Drug; Female; Follow-Up Studies; Glucocorticoids; Hum | 2017 |
IMPAIRED ALDOSTERONE PRODUCTION IN "SALT-LOSING" CONGENITAL ADRENAL HYPERPLASIA.
Topics: Adrenal Hyperplasia, Congenital; Adrenogenital Syndrome; Aldosterone; Child; Chromatography; Humans; | 1965 |
Cobalamin C disease presenting with hemophagocytic lymphohistiocytosis.
Topics: Diagnosis, Differential; Female; Hemolytic-Uremic Syndrome; Homocystinuria; Humans; Infant; Lymphohi | 2005 |
Adult onset urea cycle disorder in a patient with presumed hepatic encephalopathy.
Topics: Diagnosis, Differential; Glucocorticoids; Hepatic Encephalopathy; Humans; Hyperammonemia; Male; Meta | 2008 |
Adrenal virilism due to 21-hydroxylase deficiency in the postmenarchial female.
Topics: 17-Ketosteroids; Adolescent; Adrenal Gland Diseases; Adrenal Hyperplasia, Congenital; Adrenocorticot | 1975 |
Liver transplantation.
Topics: Adult; Age Factors; Animals; Antilymphocyte Serum; Azathioprine; Biliary Tract; Child; Dogs; Graft R | 1978 |
[Weber-Christian disease associated with familial alpha-1-antitrypsin deficiency. Apropos of a case].
Topics: alpha 1-Antitrypsin Deficiency; Female; Humans; Metabolism, Inborn Errors; Middle Aged; Panniculitis | 1985 |
Steroidal and gonadotropin evaluation of a patient with a feminizing tumor of the adrenal gland. In vivo and in vitro studies.
Topics: 17-Hydroxycorticosteroids; 17-Ketosteroids; Adrenal Gland Neoplasms; Adrenalectomy; Chromatography; | 1969 |
Hypophosphatasia: clinical and metabolic studies.
Topics: Adolescent; Alkaline Phosphatase; Body Height; Body Weight; Bone Diseases; Calcium; Cephalometry; Ch | 1968 |
[On hypophosphatasia].
Topics: Bone Diseases; Humans; Hypophosphatasia; Metabolism, Inborn Errors; Phosphoric Monoester Hydrolases; | 1967 |
Chronic hemolytic anemia associated with erythrocyte enolase deficiency exacerbated by ingestion of nitrofurantoin.
Topics: Anemia, Hemolytic, Congenital; Erythrocytes; Female; Hematocrit; Humans; Metabolism, Inborn Errors; | 1972 |
Lipid storage myopathy: a recognizable clinicopathological entity?
Topics: Adult; Humans; Lipid Metabolism; Lipids; Male; Metabolism, Inborn Errors; Mitochondria, Muscle; Musc | 1973 |
Experience with long-term therapy in congenital adrenal hyperplasia.
Topics: 17-Ketosteroids; Adolescent; Adrenocortical Hyperfunction; Body Height; Bone Development; Child; Chi | 1974 |
Enterocyte in coeliac disease. 1.
Topics: Alkaline Phosphatase; Celiac Disease; Diet Therapy; Female; Glutens; Glycoside Hydrolases; Humans; I | 1970 |