urea has been researched along with Glycogenosis in 6 studies
pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.
| Excerpt | Relevance | Reference |
|---|---|---|
| " Specific illustrative inborn errors of metabolism are discussed (aminoacidemias, urea cycle defects, organic acidemias, fatty acid oxidation defects, disorders of carbohydrate metabolism, lysosomal storage disorders) in light of potential problems encountered in adolescence and adulthood, including issues involving pregnancy and long-term medical, psychosocial, and psychiatric complications." | 4.81 | The adolescent with an inborn error of metabolism: medical issues and transition to adulthood. ( Enns, GM; Packman, W, 2002) |
| "Hepatocyte glycogen accumulation in urea cycle enzyme defects resembles that seen in glycogen storage disease but can be distinguished in most cases by non-uniformity of distribution and/or the absence of sinusoidal compression by expanded hepatocytes." | 3.73 | Hepatocyte glycogen accumulation in patients undergoing dietary management of urea cycle defects mimics storage disease. ( Bove, KE; Heubi, JE; Miles, L, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (50.00) | 18.7374 |
| 1990's | 1 (16.67) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Miles, L | 1 |
| Heubi, JE | 1 |
| Bove, KE | 1 |
| Mowat, AP | 1 |
| Badizadegan, K | 1 |
| Perez-Atayde, AR | 1 |
| Enns, GM | 1 |
| Packman, W | 1 |
| Snyderman, SE | 1 |
| Gibson, WB | 1 |
| Illingsworth, B | 1 |
| Brown, DH | 1 |
3 reviews available for urea and Glycogenosis
| Article | Year |
|---|---|
Hepatic Disorders.
Topics: Adolescent; Adult; alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Ammonia; Ch | 1982 |
The adolescent with an inborn error of metabolism: medical issues and transition to adulthood.
Topics: Adolescent; Adolescent Medicine; Adult; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolis | 2002 |
The dietary therapy of inherited metabolic disease.
Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Child; C | 1975 |
3 other studies available for urea and Glycogenosis
| Article | Year |
|---|---|
Hepatocyte glycogen accumulation in patients undergoing dietary management of urea cycle defects mimics storage disease.
Topics: Child; Child, Preschool; Diagnosis, Differential; Glucose-6-Phosphatase; Glycogen; Glycogen Storage | 2005 |
Focal glycogenosis of the liver in disorders of ureagenesis: its occurrence and diagnostic significance.
Topics: Adolescent; Ammonia; Carbamoyl-Phosphate Synthase (Ammonia); Child; Child, Preschool; Diagnosis, Dif | 1997 |
Studies of glycogen branching enzyme. Preparation and properties of -1,4-glucan- -1,4-glucan 6-glycosyltransferase and its action on the characteristic polysaccharide of the liver of children with Type IV glycogen storage disease.
Topics: Animals; Centrifugation, Density Gradient; Child; Chromatography, Gel; Electrophoresis, Disc; Glucos | 1971 |