urea has been researched along with Deficiency, Mental in 40 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 |
|---|---|---|
| "We studied 26 children with inborn errors of urea synthesis who survived neonatal hyperammonemic coma." | 3.67 | Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies. ( Batshaw, ML; Brusilow, SW; Mellits, ED; Msall, M; Suss, R, 1984) |
| "Hypernatraemic dehydration, subclinical underhydration, and undernutrition were common in a large hospital for the mentally and physically handicapped." | 1.28 | Hypernatraemic dehydration in patients in a large hospital for the mentally handicapped. ( Dunnigan, MG; Macdonald, NJ; McConnell, KN; Stephen, MR, 1989) |
| "The infant developed severe mental retardation, athetosis, and spasticity." | 1.25 | Familial hyperargininaemia. ( Colombo, JP; Lavinha, F; Lowenthal, A; Terheggen, HG, 1975) |
| "Orotic aciduria was present (max: 693 mg/day) and was related to NH4 levels." | 1.25 | [Chronic hyperammonemia with orotic aciduria: evidence of pyrimidine pathway stimulation (author's transl)]. ( Beaudry, MA; Collu, R; Dallairf, L; Ducharme, JR; Leboeuf, G; Letarte, J; Melancon, SB, 1975) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 34 (85.00) | 18.7374 |
| 1990's | 1 (2.50) | 18.2507 |
| 2000's | 5 (12.50) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| SCHLESINGER, B | 1 |
| CLAYTON, B | 1 |
| BODIAN, M | 1 |
| JONES, KV | 1 |
| BRUNE, GG | 1 |
| HOHL, HH | 1 |
| HIMWICH, HE | 1 |
| HOEFNAGEL, D | 1 |
| MCMURRAY, WC | 2 |
| MOHYUDDIN, F | 2 |
| RATHBUN, JC | 2 |
| Wallace, RA | 1 |
| Schluter, PJ | 1 |
| Forgan-Smith, R | 1 |
| Wood, R | 1 |
| Webb, PM | 1 |
| Pérez Valdivieso, JR | 1 |
| Mbongo Bubakala, CL | 1 |
| Calderón Pelayo, R | 1 |
| López Olaondo, LA | 1 |
| Bes Rastrollo, M | 1 |
| Bachmann, C | 1 |
| Gropman, AL | 1 |
| Batshaw, ML | 3 |
| Levin, B | 1 |
| Miller, AL | 1 |
| McLean, P | 1 |
| Morrow, G | 1 |
| Barness, LA | 1 |
| Efron, ML | 1 |
| Wu, WK | 1 |
| Nyhan, WL | 1 |
| Msall, M | 1 |
| Suss, R | 1 |
| Brusilow, SW | 1 |
| Mellits, ED | 1 |
| Tada, K | 1 |
| Tateda, H | 1 |
| Metoki, K | 1 |
| Painter, MJ | 1 |
| Sproul, GT | 1 |
| Schafer, IA | 1 |
| Thomas, GH | 1 |
| Brusilow, S | 1 |
| Whitington, PF | 1 |
| Alonso, EM | 1 |
| Boyle, JT | 1 |
| Molleston, JP | 1 |
| Rosenthal, P | 1 |
| Emond, JC | 1 |
| Millis, JM | 1 |
| Kamoun, P | 1 |
| Rabier, D | 1 |
| Saudubray, JM | 1 |
| Shambaugh, GE | 1 |
| Terheggen, HG | 1 |
| Lowenthal, A | 1 |
| Lavinha, F | 1 |
| Colombo, JP | 3 |
| Simell, O | 1 |
| Perheentupa, J | 2 |
| Rapola, J | 1 |
| Visakorpi, JK | 2 |
| Eskelin, LE | 1 |
| Beaudry, MA | 1 |
| Letarte, J | 1 |
| Collu, R | 1 |
| Leboeuf, G | 1 |
| Ducharme, JR | 1 |
| Melancon, SB | 1 |
| Dallairf, L | 1 |
| Macdonald, NJ | 1 |
| McConnell, KN | 1 |
| Stephen, MR | 1 |
| Dunnigan, MG | 1 |
| Lynch, DM | 1 |
| Eliatamby, CL | 1 |
| Anderson, AA | 1 |
| Turova, NF | 1 |
| Ermolina, LA | 1 |
| Baryshnikov, VA | 1 |
| Gertenrich, RL | 1 |
| Brown, CA | 1 |
| Cederbaum, SD | 1 |
| Shaw, KN | 1 |
| Valente, M | 1 |
| Cotton, ME | 1 |
| Martin, JJ | 1 |
| Schlote, W | 1 |
| Brown, JH | 1 |
| Fabre, LF | 1 |
| Farrell, GL | 1 |
| Adams, ED | 1 |
| Eldjarn, L | 2 |
| Jellum, E | 2 |
| Stokke, O | 2 |
| Scott-Emuakpor, A | 1 |
| Higgins, JV | 1 |
| Kohrman, AF | 1 |
| Norio, R | 1 |
| Kekomäki, M | 1 |
| Corbeel, LM | 1 |
| Van Sande, M | 1 |
| Weber, A | 1 |
| Jagenburg, R | 2 |
| Lindstedt, G | 2 |
| Malmquist, J | 2 |
| Kluge, T | 1 |
| Börresen, HC | 1 |
| Gillen, HW | 1 |
| Pippinger, CE | 1 |
| Hopkins, IJ | 1 |
| Connelly, JF | 1 |
| Hocking, B | 1 |
| Maddison, TG | 1 |
3 reviews available for urea and Deficiency, Mental
| Article | Year |
|---|---|
Cognitive outcome in urea cycle disorders.
Topics: Age of Onset; Child; Cognition Disorders; Female; Humans; Hyperammonemia; Intellectual Disability; M | 2004 |
Understanding inherited metabolic disease.
Topics: Amniocentesis; Carboxy-Lyases; Female; Genetic Carrier Screening; Homocystinuria; Humans; Infant, Ne | 1980 |
Urea biosynthesis II. Normal and abnormal regulation.
Topics: Adrenal Cortex Hormones; Adrenal Glands; Ammonia; Animals; Argininosuccinate Synthase; Argininosucci | 1978 |
2 trials available for urea and Deficiency, Mental
| Article | Year |
|---|---|
Pipothiazine palmitate in the management of aggressive mentally handicapped patients.
Topics: Adult; Aggression; Antipsychotic Agents; Clinical Trials as Topic; Double-Blind Method; Female; Huma | 1985 |
Treatment of Dilantin gingival hyperplasia with Proxigel.
Topics: Adult; Clinical Trials as Topic; Drug Evaluation; Female; Gels; Gingival Hyperplasia; Gingivitis; Hu | 1974 |
35 other studies available for urea and Deficiency, Mental
| Article | Year |
|---|---|
TYPUS DEGENERATIVUS AMSTELODAMENSIS.
Topics: 17-Ketosteroids; Adrenal Cortex Hormones; Adrenal Glands; Adrenocorticotropic Hormone; Blood Chemica | 1963 |
URINARY EXCRETION OF BUFOTENIN-LIKE SUBSTANCE IN PSYCHOTIC PATIENTS.
Topics: 1-Propanol; Acetates; Alcohols; Alkaloids; Ammonia; Bufotenin; Chromatography; Hallucinogens; Humans | 1963 |
THE SYNDROME OF ATHETOID CEREBRAL PALSY, MENTAL DEFICIENCY, SELF-MUTILATION AND HYPERURICEMIA.
Topics: Athetosis; Blood Chemical Analysis; Blood Urea Nitrogen; Cerebral Palsy; Child; Genetics, Medical; H | 1965 |
CITRULLINURIA.
Topics: Amino Acid Metabolism, Inborn Errors; Citrulline; Citrullinemia; Clinical Enzyme Tests; Humans; Infa | 1964 |
Diagnosis of Helicobacter pylori infection in adults with intellectual disability.
Topics: Adult; Antibodies, Bacterial; Antigens, Bacterial; Breath Tests; Caregivers; Feces; Helicobacter Inf | 2003 |
[Anesthetic considerations in a woman with congenital hyperammonemia].
Topics: Adult; Anesthesia, General; Epilepsy; Fasting; Female; Humans; Hyperammonemia; Intellectual Disabili | 2002 |
Long-term outcome of patients with urea cycle disorders and the question of neonatal screening.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Argininosuccinic Acid; Child; Citrullin | 2003 |
Studies on amino acid metabolism in citrullinuria.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Blood Chemical Analysis; Caseins; Child; | 1967 |
Arginosuccine aciduria.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Child; Citrates; Diet Therapy; Glutamates; | 1967 |
Urea cycle enzymes in the liver of a patient with argininosuccinic aciduria.
Topics: Acids; Adolescent; Adult; Alkaline Phosphatase; Animals; Arginine; Clinical Enzyme Tests; Electroenc | 1967 |
Citrullinemia with defective urea production.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Diet Therapy; Female; Humans; Infant; In | 1967 |
Inborn metabolic errors of urea cycle.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Chromatography; Humans; Intellectual Disability; Ure | 1967 |
Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Argininosuccinate Synthase; Argininosuccinic Aciduria | 1984 |
A new method for screening of hyperammonemia.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Humans; Infant, Newborn; Intellectual Disability; Mas | 1982 |
Therapy of urea cycle enzymopathies: three case studies.
Topics: Ammonia; Arginine; Argininosuccinic Acid; Argininosuccinic Aciduria; Child, Preschool; Citrulline; C | 1981 |
Liver transplantation for the treatment of urea cycle disorders.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Canada; Carbamoyl-Phosphate Synthase (Ammonia); Child | 1998 |
A risk factor for chronic mild hyperammonaemia.
Topics: Child; Chronic Disease; Humans; Hyperammonemia; Intellectual Disability; Risk Factors; Urea | 2002 |
Familial hyperargininaemia.
Topics: Amino Acids; Ammonia; Arginine; Athetosis; Child, Preschool; Chromatography; Cystinuria; Dietary Pro | 1975 |
Lysinuric protein intolerance.
Topics: Adolescent; Adult; Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Arginine; Bi | 1975 |
[Chronic hyperammonemia with orotic aciduria: evidence of pyrimidine pathway stimulation (author's transl)].
Topics: Alanine; Amino Acids; Ammonia; Child, Preschool; Dietary Proteins; Erythrocytes; Growth Disorders; H | 1975 |
Hypernatraemic dehydration in patients in a large hospital for the mentally handicapped.
Topics: Adult; Aged; Aged, 80 and over; Body Mass Index; Creatinine; Dehydration; Disabled Persons; Feeding | 1989 |
[Characteristics of the amino acid spectrum of the blood of children with intellectual deficiency].
Topics: Amino Acids; Ammonia; Arginine; Aspartic Acid; Child; Female; Glutamates; Glutamic Acid; Humans; Int | 1986 |
[Enzymatic disturbances in the urea cycle].
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Child; Child, Preschool; Cit | 1969 |
Argininosuccinic aciduria.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Chromatography, Thin Layer; Citric Acid | 1973 |
Central nervous system lesions in disorders of amino-acid metabolism. A neuropathological study.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Brain; Central Nervous System; Chi | 1972 |
Hyperlysinuria with hyperammonemia. A new metabolic disorder.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Diet Therapy; Growth Disorders; | 1972 |
Pyroglutamic aciduria: studies on the enzymic block and on the metabolic origin of pyroglutamic acid.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Bicarbonates; Biodegradation, Environmenta | 1972 |
Citrullinemia: a new case, with implications concerning adaptation to defective urea synthesis.
Topics: Adult; Amino Acids; Ammonia; Citrulline; Dietary Proteins; Fibroblasts; Humans; Intellectual Disabil | 1972 |
Lysinuric protein intolerance, an autosomal recessive disease. A genetic study of 10 Finnish families.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Body Height; Consanguinity; Female; Finland; Gene | 1971 |
Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis.
Topics: Ammonia; Coma; Diet Therapy; Female; Humans; Infant; Intellectual Disability; Liver; Metabolism, Inb | 1969 |
[Familial protein intolerance with hyperammonemia].
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Female; Humans; Intellectual Disability; Nitrogen; Urea | 1970 |
Pyroglutamic aciduria--a new inborn error of metabolism.
Topics: Acidosis; Adult; Amino Acids; Brain Damage, Chronic; Chromatography, Gas; Chromatography, Ion Exchan | 1970 |
Familial protein intolerance. Possible nature of enzyme defect.
Topics: Adult; Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Atrophy; Biological Tran | 1971 |
Low specific gravity syndrome.
Topics: Adult; Anticonvulsants; Calcium; Chlorides; Chronic Disease; Creatinine; Epilepsy; Female; Humans; I | 1968 |
Neurological abnormalities in primary hyperammonaemia.
Topics: Ammonia; Diet Therapy; Dietary Proteins; Female; Humans; Infant; Intellectual Disability; Lysine; Me | 1968 |