urea has been researched along with Rett Syndrome in 3 studies
pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.
Rett Syndrome: An inherited neurological developmental disorder that is associated with X-LINKED INHERITANCE and may be lethal in utero to hemizygous males. The affected female is normal until the age of 6-25 months when progressive loss of voluntary control of hand movements and communication skills; ATAXIA; SEIZURES; autistic behavior; intermittent HYPERVENTILATION; and HYPERAMMONEMIA appear. (From Menkes, Textbook of Child Neurology, 5th ed, p199)
Excerpt | Relevance | Reference |
---|---|---|
"The in vivo functioning of the urea cycle in the Rett syndrome (RS) was investigated using alanine load test." | 7.68 | The urea cycle in the Rett syndrome. ( Hjelm, M; Oberholzer, V; Thomas, S; Wilson, J, 1990) |
"The in vivo functioning of the urea cycle in the Rett syndrome (RS) was investigated using alanine load test." | 3.68 | The urea cycle in the Rett syndrome. ( Hjelm, M; Oberholzer, V; Thomas, S; Wilson, J, 1990) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 3 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Burd, L | 1 |
Kemp, R | 1 |
Knull, H | 1 |
Loveless, D | 1 |
Clarke, A | 1 |
Gardner-Medwin, D | 1 |
Richardson, J | 1 |
McGann, A | 1 |
Bonham, JR | 1 |
Carpenter, KH | 1 |
Bhattacharya, S | 1 |
Haggerty, D | 1 |
Fleetwood, JA | 1 |
Aynsley-Green, A | 1 |
Thomas, S | 1 |
Oberholzer, V | 1 |
Wilson, J | 1 |
Hjelm, M | 1 |
1 review available for urea and Rett Syndrome
Article | Year |
---|---|
A review of the biochemical pathways studied and abnormalities reported in the Rett syndrome.
Topics: Biogenic Amines; Carnitine; Energy Metabolism; Glutarates; Goals; Humans; Neurotransmitter Agents; R | 1990 |
2 other studies available for urea and Rett Syndrome
Article | Year |
---|---|
Abnormalities of carbohydrate metabolism and of OCT gene function in the Rett syndrome.
Topics: Adolescent; Carbohydrate Metabolism; Child; Child, Preschool; Female; Genetic Linkage; Humans; Metab | 1990 |
The urea cycle in the Rett syndrome.
Topics: Adult; Ammonia; Child; Child, Preschool; Female; Humans; Middle Aged; Orotic Acid; Rett Syndrome; Ur | 1990 |