urea has been researched along with Acquired Metabolic Diseases, Brain in 13 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 |
|---|---|---|
| "Ornithine transcarbamylase deficiency is the most common inherited urea cycle disorder." | 6.43 | [Hyperammonemia type II as an example of urea cycle disorder]. ( Duława, J; Hawrot-Kawecka, AM; Kawecki, GP, 2006) |
| " Disruptions of glutamate metabolism have been implicated in other clinical disorders, such as pyridoxine-dependent seizures, confirming the importance of intact glutamate metabolism." | 4.81 | Disorders of glutamate metabolism. ( Kelly, A; Stanley, CA, 2001) |
| "Ornithine transcarbamylase deficiency is the most common inherited urea cycle disorder." | 2.43 | [Hyperammonemia type II as an example of urea cycle disorder]. ( Duława, J; Hawrot-Kawecka, AM; Kawecki, GP, 2006) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (7.69) | 18.2507 |
| 2000's | 8 (61.54) | 29.6817 |
| 2010's | 4 (30.77) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Acosta, P | 1 |
| Nogueira, M | 1 |
| Gallagher, R | 1 |
| Waquim, C | 1 |
| Piroli, I | 1 |
| Carmona, R | 1 |
| Centeno, M | 1 |
| Motto, E | 1 |
| Jáčová, J | 1 |
| Jořenek, M | 1 |
| Pospíšková, K | 1 |
| Najdekr, L | 1 |
| Zajoncová, L | 1 |
| Friedecký, D | 1 |
| Adam, T | 1 |
| Singh, S | 1 |
| Suresh, S | 1 |
| McClave, SA | 1 |
| Cave, M | 1 |
| Sehli, S | 1 |
| Nugent, KM | 1 |
| Samathanam, CA | 1 |
| Alalawi, R | 1 |
| da Rocha, AJ | 1 |
| Maia, AC | 1 |
| da Silva, CJ | 1 |
| Sachetti, SB | 1 |
| Wasant, P | 1 |
| Srisomsap, C | 1 |
| Liammongkolkul, S | 1 |
| Svasti, J | 1 |
| Hawrot-Kawecka, AM | 1 |
| Kawecki, GP | 1 |
| Duława, J | 1 |
| Roze, E | 1 |
| Azuar, C | 1 |
| Menuel, C | 1 |
| Häberle, J | 1 |
| Guillevin, R | 1 |
| Morris, AA | 1 |
| Leonard, JV | 1 |
| Mathias, RS | 1 |
| Kostiner, D | 1 |
| Packman, S | 1 |
| Kölker, S | 1 |
| Okun, JG | 1 |
| Hörster, F | 1 |
| Assmann, B | 1 |
| Ahlemeyer, B | 1 |
| Kohlmüller, D | 1 |
| Exner-Camps, S | 1 |
| Mayatepek, E | 1 |
| Krieglstein, J | 1 |
| Hoffmann, GF | 1 |
| Butterworth, RF | 1 |
| Kelly, A | 1 |
| Stanley, CA | 1 |
6 reviews available for urea and Acquired Metabolic Diseases, Brain
| Article | Year |
|---|---|
Treating Every Needle in the Haystack: Hyperammonemic Encephalopathy and Severe Malnutrition After Bariatric Surgery-A Case Report and Review of the Literature.
Topics: Adult; Ammonia; Brain Diseases, Metabolic; Diagnostic Errors; Female; Fibrosis; Gastric Bypass; Huma | 2015 |
[Hyperammonemia type II as an example of urea cycle disorder].
Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Coma; Female; Humans; Hyperammonemi | 2006 |
Early recognition of metabolic decompensation.
Topics: Biomarkers; Brain Diseases, Metabolic; Child; Fatty Acids; Glycogen Storage Disease Type I; Humans; | 1997 |
Hyperammonemia in urea cycle disorders: role of the nephrologist.
Topics: Algorithms; Ammonia; Brain Diseases, Metabolic; Child, Preschool; Coma; Developmental Disabilities; | 2001 |
Glutamate transporter and receptor function in disorders of ammonia metabolism.
Topics: Adenosine Triphosphate; Amino Acid Transport System X-AG; Ammonia; Apoptosis; Astrocytes; Binding Si | 2001 |
Disorders of glutamate metabolism.
Topics: Acetyltransferases; Amino-Acid N-Acetyltransferase; ATP-Binding Cassette Transporters; Bacterial Pro | 2001 |
7 other studies available for urea and Acquired Metabolic Diseases, Brain
| Article | Year |
|---|---|
[Hyperammonemic encephalopathy due to urinary tract infection by urea splitting bacteria. A pediatric case report].
Topics: Brain Diseases, Metabolic; Child, Preschool; Corynebacterium Infections; Humans; Hyperammonemia; Mal | 2017 |
Urease-immobilized magnetic microparticles in urine sample preparation for metabolomic analysis by gas chromatography-mass spectrometry.
Topics: Amino Acid Metabolism, Inborn Errors; Analytic Sample Preparation Methods; Brain Diseases, Metabolic | 2019 |
An 18-year-old woman with hyperammonemia.
Topics: Adolescent; Brain Diseases, Metabolic; Fatal Outcome; Female; Humans; Hyperammonemia; Metabolism, In | 2009 |
Lentiform fork sign in a child with dialysis disequilibrium syndrome: a transient MRI pattern which emphasizes neurologic consequence of metabolic acidosis.
Topics: Acidosis; Basal Ganglia; Blood Urea Nitrogen; Brain Diseases, Metabolic; Brain Edema; Child; Corpus | 2013 |
Urea cycle disorders in Thai infants: a report of 5 cases.
Topics: Argininosuccinate Synthase; Brain Diseases, Metabolic; Child Development; Fatal Outcome; Female; Hum | 2002 |
Usefulness of magnetic resonance spectroscopy in urea cycle disorders.
Topics: Adult; Argininosuccinic Aciduria; Brain Diseases, Metabolic; Creatine; Female; Humans; Magnetic Reso | 2007 |
3-Ureidopropionate contributes to the neuropathology of 3-ureidopropionase deficiency and severe propionic aciduria: a hypothesis.
Topics: Animals; beta-Alanine; Brain Diseases, Metabolic; Calcium; Cell Death; Cells, Cultured; Central Nerv | 2001 |