urea has been researched along with Coma in 48 studies
pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.
Coma: A profound state of unconsciousness associated with depressed cerebral activity from which the individual cannot be aroused. Coma generally occurs when there is dysfunction or injury involving both cerebral hemispheres or the brain stem RETICULAR FORMATION.
| Excerpt | Relevance | Reference |
|---|---|---|
| "In order to examine, whether the lobeline-induced cough is a true reflex or a voluntary effort to get rid of its irritating sensations in the upper respiratory tract, we systematically studied the cough response to lobeline, of subjects who were unable to make conscious discriminations i." | 9.11 | How does lobeline injected intravenously produce a cough? ( Anand, A; Bakshi, GS; Paintal, AS; Raj, H; Tiwari, RR, 2005) |
| "The relative effectiveness of exchange transfusion, peritoneal dialysis, arginine, and sodium benzoate was evaluated during 44 episodes of hyperammonemic coma in 31 patients with congenital urea cycle enzymopathies." | 7.66 | Treatment of hyperammonemic coma caused by inborn errors of urea synthesis. ( Batshaw, ML; Brusilow, SW, 1980) |
| "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) |
| "Although a rare disorder, ornithine transcarbamylase deficiency is the most common of the urea cycle disorders, which can occur both in children, and less commonly, in adults." | 5.42 | Fatal coma in a young adult due to late-onset urea cycle deficiency presenting with a prolonged seizure: a case report. ( Alameri, M; Alsaadi, T; Shakra, M, 2015) |
| "The diagnosis of hereditary ornithine transcarbamylase deficiency was confirmed by liver biopsy in the immediate post-mortem period." | 5.31 | [Fulminant coma: think hyperammonemia and urea cycle disorders]. ( Augris, C; Benabdelmalek, F; Caramella, JP; Jouvet, P; Vauquelin, P, 2002) |
| " Urea and vaptans can be effective treatments for the syndrome of inappropriate antidiuresis and hyponatremia in patients with heart failure, but have adverse effects (eg, poor palatability and gastric intolerance with urea; and overly rapid correction of hyponatremia and increased thirst with vaptans)." | 5.22 | Diagnosis and Management of Hyponatremia: A Review. ( Adrogué, HJ; Madias, NE; Tucker, BM, 2022) |
| ", urea, glucose, sodium, and potassium) in the setting of non-local anesthetic drug overdose." | 5.16 | Lipid emulsion improves Glasgow coma scale and decreases blood glucose level in the setting of acute non-local anesthetic drug poisoning--a randomized controlled trial. ( Sanaei-Zadeh, H; Sepehrian, B; Taftachi, F; Zamani, N, 2012) |
| "In order to examine, whether the lobeline-induced cough is a true reflex or a voluntary effort to get rid of its irritating sensations in the upper respiratory tract, we systematically studied the cough response to lobeline, of subjects who were unable to make conscious discriminations i." | 5.11 | How does lobeline injected intravenously produce a cough? ( Anand, A; Bakshi, GS; Paintal, AS; Raj, H; Tiwari, RR, 2005) |
| " The factors are more common in cases with high mortality with diastolic blood pressure (DBP) below 60 mm of Hg, anaemia, persistence of Glasgow Coma Score below 5 on day 2, high parasite count at presentation, proteinuria and high level of serum urea." | 3.70 | Cerebral malaria--a study of 104 cases. ( Faiz, MA; Hossain, MA; Rahman, MR; Rashid, HA, 1998) |
| "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) |
| "Children with inborn errors of urea synthesis accumulate ammonium and other nitrogenous precursors of urea, leading to episodic coma and a high mortality rate." | 3.66 | Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion. ( Batshaw, ML; Blom, W; Brubakk, AM; Brusilow, S; Burton, BK; Cann, HM; Kerr, D; Mamunes, P; Matalon, R; Myerberg, D; Schafer, IA; Waber, L, 1982) |
| "The relative effectiveness of exchange transfusion, peritoneal dialysis, arginine, and sodium benzoate was evaluated during 44 episodes of hyperammonemic coma in 31 patients with congenital urea cycle enzymopathies." | 3.66 | Treatment of hyperammonemic coma caused by inborn errors of urea synthesis. ( Batshaw, ML; Brusilow, SW, 1980) |
| " Crystalluria in a three-month-old male infant with a history of intermittent vomiting since birth and incipient coma led to the discovery of orotic aciduria." | 3.65 | Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infant. ( Mackenzie, S; MacLeod, P; Scriver, CR, 1972) |
| "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) |
| "Coma was induced using a free-fall drop method." | 1.62 | Wakefulness-Promoting Effects of Lateral Hypothalamic Area-Deep Brain Stimulation in Traumatic Brain Injury-Induced Comatose Rats: Upregulation of α1-Adrenoceptor Subtypes and Downregulation of Gamma-Aminobutyric Acid β Receptor Expression Via the Orexins ( Dong, X; Feng, Z; Liu, H; Lu, G; Tang, Y; Wang, J; Xiong, J; Ye, W; Zhong, L, 2021) |
| "Although a rare disorder, ornithine transcarbamylase deficiency is the most common of the urea cycle disorders, which can occur both in children, and less commonly, in adults." | 1.42 | Fatal coma in a young adult due to late-onset urea cycle deficiency presenting with a prolonged seizure: a case report. ( Alameri, M; Alsaadi, T; Shakra, M, 2015) |
| "The diagnosis of hereditary ornithine transcarbamylase deficiency was confirmed by liver biopsy in the immediate post-mortem period." | 1.31 | [Fulminant coma: think hyperammonemia and urea cycle disorders]. ( Augris, C; Benabdelmalek, F; Caramella, JP; Jouvet, P; Vauquelin, P, 2002) |
| "Ammoniagenic coma or episodic stupor is a rare complication of ureterosigmoidostomy." | 1.27 | Ammoniagenic coma following ureterosigmoidostomy. ( Kaufman, JJ, 1984) |
| "Ammonia coma was produced in rats within 10 to 15 minutes of an intraperitonealinjection of 1." | 1.26 | Reversal of ammonia coma in rats by L-dopa: a peripheral effect. ( Derr, RF; Doizaki, WM; Zieve, L, 1979) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 29 (60.42) | 18.7374 |
| 1990's | 5 (10.42) | 18.2507 |
| 2000's | 8 (16.67) | 29.6817 |
| 2010's | 4 (8.33) | 24.3611 |
| 2020's | 2 (4.17) | 2.80 |
| Authors | Studies |
|---|---|
| Adrogué, HJ | 1 |
| Tucker, BM | 1 |
| Madias, NE | 1 |
| Dong, X | 1 |
| Ye, W | 1 |
| Tang, Y | 1 |
| Wang, J | 1 |
| Zhong, L | 1 |
| Xiong, J | 2 |
| Liu, H | 1 |
| Lu, G | 1 |
| Feng, Z | 1 |
| Alameri, M | 1 |
| Shakra, M | 1 |
| Alsaadi, T | 1 |
| Açıkalın, A | 1 |
| Dişel, NR | 1 |
| Anand, JS | 1 |
| Kabata, P | 1 |
| Jia, X | 1 |
| Yan, J | 1 |
| Xia, J | 1 |
| Wang, T | 1 |
| Chen, Y | 1 |
| Qi, A | 1 |
| Yang, N | 1 |
| Fan, S | 1 |
| Ye, J | 1 |
| Hu, Z | 1 |
| Taftachi, F | 1 |
| Sanaei-Zadeh, H | 1 |
| Sepehrian, B | 1 |
| Zamani, N | 1 |
| Augris, C | 1 |
| Jouvet, P | 1 |
| Benabdelmalek, F | 1 |
| Vauquelin, P | 1 |
| Caramella, JP | 1 |
| ARNAUD, P | 2 |
| DALMAIS, J | 2 |
| PLAUCHU, M | 2 |
| VALLADE, L | 1 |
| HUGONENQ, H | 1 |
| JUDE, JP | 1 |
| MELLANDER, R | 1 |
| MCKENDRY, JB | 1 |
| BUTTARO, CA | 1 |
| TRAMONTANA, C | 1 |
| GUAITINI, V | 1 |
| LEVY, VG | 1 |
| BERGOZ, R | 1 |
| PREVOT, M | 1 |
| LAUGA, J | 1 |
| CAROLI, J | 1 |
| MULLAN, D | 1 |
| PLATTS, M | 1 |
| RIDGWAY, B | 1 |
| Raj, H | 1 |
| Bakshi, GS | 1 |
| Tiwari, RR | 1 |
| Anand, A | 1 |
| Paintal, AS | 1 |
| Hillman, J | 1 |
| Milos, P | 1 |
| Yu, ZQ | 1 |
| Sjögren, F | 1 |
| Anderson, C | 1 |
| Mellergård, P | 1 |
| Hawrot-Kawecka, AM | 1 |
| Kawecki, GP | 1 |
| Duława, J | 1 |
| Fadel, N | 1 |
| Bochereau, G | 1 |
| Kragen, MT | 1 |
| Chauveau, P | 1 |
| Uhart, N | 1 |
| Kaufman, JJ | 1 |
| Msall, M | 1 |
| Batshaw, ML | 4 |
| Suss, R | 1 |
| Brusilow, SW | 3 |
| Mellits, ED | 1 |
| Brusilow, S | 2 |
| Waber, L | 1 |
| Blom, W | 1 |
| Brubakk, AM | 1 |
| Burton, BK | 1 |
| Cann, HM | 1 |
| Kerr, D | 1 |
| Mamunes, P | 1 |
| Matalon, R | 1 |
| Myerberg, D | 1 |
| Schafer, IA | 2 |
| Painter, MJ | 1 |
| Sproul, GT | 1 |
| Thomas, GH | 2 |
| Jaffar, S | 1 |
| Van Hensbroek, MB | 1 |
| Palmer, A | 1 |
| Schneider, G | 1 |
| Greenwood, B | 1 |
| Faiz, MA | 1 |
| Rahman, MR | 1 |
| Hossain, MA | 1 |
| Rashid, HA | 1 |
| Hawley, RJ | 1 |
| Mathias, RS | 1 |
| Kostiner, D | 1 |
| Packman, S | 1 |
| Vainstein, G | 1 |
| Korzets, Z | 1 |
| Pomeranz, A | 1 |
| Gadot, N | 1 |
| Winchester, JF | 1 |
| Gelfand, MC | 1 |
| Knepshield, JH | 1 |
| Schreiner, GE | 1 |
| Zieve, L | 1 |
| Doizaki, WM | 1 |
| Derr, RF | 1 |
| Arena, JM | 1 |
| Silver, SM | 1 |
| DeSimone, JA | 1 |
| Smith, DA | 1 |
| Sterns, RH | 1 |
| Kaveggia, FF | 1 |
| Thompson, JS | 1 |
| Schafer, EC | 1 |
| Fischer, JL | 1 |
| Taylor, RJ | 1 |
| Arn, PH | 1 |
| Hauser, ER | 1 |
| Herman, G | 1 |
| Hess, D | 1 |
| Saudubray, JM | 1 |
| Lyonnet, S | 1 |
| Lombes, A | 1 |
| Hervé, F | 1 |
| Bonnefont, JP | 1 |
| Munnich, A | 1 |
| Ogier, H | 1 |
| Watschinger, B | 1 |
| Bodin, F | 1 |
| Liguory, C | 1 |
| Capelle, P | 1 |
| Conte, M | 1 |
| Kang, ES | 1 |
| Snodgrass, PJ | 1 |
| Gerald, PS | 1 |
| Feng, PH | 1 |
| Cheah, PS | 1 |
| Lee, YK | 1 |
| Baethke, R | 1 |
| Scholz, A | 1 |
| Day, S | 1 |
| Buckell, M | 2 |
| Sunshine, P | 1 |
| Lindenbaum, JE | 1 |
| Levy, HL | 1 |
| Freeman, JM | 1 |
| MacLeod, P | 1 |
| Mackenzie, S | 1 |
| Scriver, CR | 1 |
| Kingston, ME | 1 |
| Corbeel, LM | 1 |
| Colombo, JP | 1 |
| Van Sande, M | 1 |
| Weber, A | 1 |
| Richardson, A | 1 |
| Sarner, M | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| The NIH UNI Study: Urea Cycle Disorders, Nutrition and Immunity[NCT01421888] | 4 participants (Actual) | Observational | 2011-08-08 | Terminated | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
5 reviews available for urea and Coma
| Article | Year |
|---|---|
Diagnosis and Management of Hyponatremia: A Review.
Topics: Coma; Heart Failure; Humans; Hyponatremia; Hypovolemia; Inappropriate ADH Syndrome; Prospective Stud | 2022 |
[Hyperammonemia type II as an example of urea cycle disorder].
Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Coma; Female; Humans; Hyperammonemi | 2006 |
Hyperammonemia in urea cycle disorders: role of the nephrologist.
Topics: Algorithms; Ammonia; Brain Diseases, Metabolic; Child, Preschool; Coma; Developmental Disabilities; | 2001 |
Protein deprivation refeeding and ammonia intoxication.
Topics: Amino Acids; Ammonia; Ammonium Chloride; Animals; Biotransformation; Coma; Dietary Proteins; Humans; | 1976 |
[Uremic coma from the viewpoints of modern therapy].
Topics: Acidosis, Renal Tubular; Acute Kidney Injury; Blood Urea Nitrogen; Carbon Isotopes; Carbonates; Coma | 1969 |
2 trials available for urea and Coma
| Article | Year |
|---|---|
Lipid emulsion improves Glasgow coma scale and decreases blood glucose level in the setting of acute non-local anesthetic drug poisoning--a randomized controlled trial.
Topics: Adult; Antidotes; Blood Gas Analysis; Blood Glucose; Coma; Drug Overdose; Drug-Related Side Effects | 2012 |
How does lobeline injected intravenously produce a cough?
Topics: Adult; Brain Injuries; Carbamide Peroxide; Coma; Cough; Dose-Response Relationship, Drug; Drug Combi | 2005 |
41 other studies available for urea and Coma
| Article | Year |
|---|---|
Wakefulness-Promoting Effects of Lateral Hypothalamic Area-Deep Brain Stimulation in Traumatic Brain Injury-Induced Comatose Rats: Upregulation of α1-Adrenoceptor Subtypes and Downregulation of Gamma-Aminobutyric Acid β Receptor Expression Via the Orexins
Topics: Anesthesia; Animals; Benzoxazoles; Brain Injuries, Traumatic; Coma; Consciousness; Deep Brain Stimul | 2021 |
Fatal coma in a young adult due to late-onset urea cycle deficiency presenting with a prolonged seizure: a case report.
Topics: Adolescent; Clostridioides difficile; Coma; Enterocolitis, Pseudomembranous; Fatal Outcome; Humans; | 2015 |
A rare cause of postpartum coma: isolated hyperammonemia due to urea cycle disorder.
Topics: Ammonia; Coma; Female; Humans; Hyperammonemia; Ornithine Carbamoyltransferase Deficiency Disease; Po | 2016 |
Acute exposure to urea.
Topics: Adult; Burns, Chemical; Chronic Disease; Coma; Drug Overdose; Environmental Exposure; Follow-Up Stud | 2009 |
Arousal effects of orexin A on acute alcohol intoxication-induced coma in rats.
Topics: Alcoholic Intoxication; Animals; Arousal; Benzoxazoles; Brain; Coma; Consciousness; Electroencephalo | 2012 |
[Fulminant coma: think hyperammonemia and urea cycle disorders].
Topics: Adolescent; Ammonia; Coma; Family; Fatal Outcome; Humans; Hyperammonemia; Male; Ornithine Carbamoylt | 2002 |
[Hypoglycemic coma during treatment of a diabetic with D 860 (dolipol)].
Topics: Coma; Diabetes Mellitus; Hypoglycemic Agents; Sulfanilamide; Sulfanilamides; Sulfonamides; Tolbutami | 1957 |
[Hypoglycemic coma during treatment of a diabetic with D 860 (dolipol)].
Topics: Coma; Diabetes Mellitus; Hypoglycemic Agents; Sulfanilamide; Sulfanilamides; Sulfonamides; Tolbutami | 1957 |
[Hypoglycemic coma during treatment of a diabetic with D 860 (dolipol)].
Topics: Coma; Diabetes Mellitus; Hypoglycemic Agents; Sulfanilamide; Sulfanilamides; Sulfonamides; Tolbutami | 1957 |
[Hypoglycemic coma during treatment of a diabetic with D 860 (dolipol)].
Topics: Coma; Diabetes Mellitus; Hypoglycemic Agents; Sulfanilamide; Sulfanilamides; Sulfonamides; Tolbutami | 1957 |
[Experiments in including hypoglycemic comas by a combination of insulin & the oral hypoglycemic sulfonamide BZ 55].
Topics: Coma; Convulsive Therapy; Hypoglycemic Agents; Insulin; Sulfanilamide; Sulfanilamides; Sulfonamides; | 1957 |
[A case of hypoglycemic coma in invenol therapy of diabetes mellitus].
Topics: Coma; Diabetes Mellitus; Hypoglycemia; Hypoglycemic Agents; Sulfanilamide; Sulfanilamides; Urea | 1957 |
Fatal hypoglycaemic coma from the use of tolbutamide (orinase).
Topics: Coma; Hypoglycemia; Hypoglycemic Agents; Pancreatic Diseases; Tolbutamide; Urea | 1957 |
[Hypoglycemic coma in diabetics treated with sulfabutyl urea (BZ 55)].
Topics: Coma; Diabetes Mellitus; Hypoglycemia; Hypoglycemic Agents; Sulfanilamide; Sulfanilamides; Urea | 1957 |
[CASE OF PERITONEAL DIALYSIS IN A PATIENT WITH CIRRHOSIS IN COMA WITH INFECTED ASCITES].
Topics: Ammonia; Ascites; Blood Chemical Analysis; Coma; Dialysis; Fluid Therapy; Hematocrit; Hepatic Enceph | 1964 |
BARBITURATE INTOXICATION.
Topics: Amobarbital; Barbiturates; Coma; Diagnosis; Electrocardiography; Hypnotics and Sedatives; Hypoxia, B | 1965 |
Intracerebral microdialysis in neurosurgical intensive care patients utilising catheters with different molecular cut-off (20 and 100 kD).
Topics: Brain Chemistry; Brain Injuries; Catheters, Indwelling; Cerebral Cortex; Coma; Critical Care; Extrac | 2006 |
[Hypo-azotemia in comas caused by voluntary drug poisoning].
Topics: Coma; Humans; Psychotropic Drugs; Urea | 1983 |
Ammoniagenic coma following ureterosigmoidostomy.
Topics: Adolescent; Adult; Ammonia; Bladder Exstrophy; Child; Child, Preschool; Colon, Sigmoid; Coma; Humans | 1984 |
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 |
Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Essential; Ammonia; Arginine; Argininosuccinate S | 1982 |
Treatment of hyperammonemic coma caused by inborn errors of urea synthesis.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Benzoates; Child; Child, | 1980 |
Therapy of urea cycle enzymopathies: three case studies.
Topics: Ammonia; Arginine; Argininosuccinic Acid; Argininosuccinic Aciduria; Child, Preschool; Citrulline; C | 1981 |
Predictors of a fatal outcome following childhood cerebral malaria.
Topics: Age Factors; Analysis of Variance; Child; Child, Preschool; Coma; Female; Gambia; Humans; Hypoglycem | 1997 |
Cerebral malaria--a study of 104 cases.
Topics: Adult; Anemia; Animals; Cause of Death; Coma; Endemic Diseases; Female; Fever; Glasgow Coma Scale; H | 1998 |
Hyperammonia possibly due to corticosteroids.
Topics: Adrenal Cortex Hormones; Ammonia; Carpal Tunnel Syndrome; Coma; Confusion; Fatal Outcome; Female; Hu | 2000 |
Deepening coma in an epileptic patient: the missing link to the urea cycle. Hyperammonaemic metabolic encephalopathy.
Topics: Anticonvulsants; Atrophy; Cerebellum; Coma; Epilepsy; Female; Humans; Hyperammonemia; Middle Aged; T | 2002 |
Present and future uses of hemoperfusion with sorbents.
Topics: Administration, Oral; Adsorption; Animals; Blood Cell Count; Blood Platelets; Charcoal; Coma; Creati | 1978 |
Reversal of ammonia coma in rats by L-dopa: a peripheral effect.
Topics: Ammonia; Ammonium Chloride; Animals; Brain; Coma; Dopamine; Levodopa; Male; Nephrectomy; Norepinephr | 1979 |
Poisoning--general treatment and prevention. Part III.
Topics: Accidents, Home; Acidosis; Antidotes; Coma; Drug Labeling; Emergencies; Health Education; Humans; In | 1975 |
Dialysis disequilibrium syndrome (DDS) in the rat: role of the "reverse urea effect".
Topics: Animals; Body Water; Brain; Brain Edema; Coma; Male; Osmolar Concentration; Rats; Rats, Inbred Strai | 1992 |
Hyperammonemic encephalopathy in urinary diversion with urea-splitting urinary tract infection.
Topics: Acidosis; Ammonia; Colon, Sigmoid; Coma; Duodenum; Female; Humans; Iatrogenic Disease; Ileum; Intest | 1990 |
Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma.
Topics: Adult; Amino Acids; Ammonia; Coma; Female; Heterozygote; Humans; Mutation; Ornithine Carbamoyltransf | 1990 |
[Urgent needs in genetics: clinical diagnosis of acute amino acid disorders of delayed onset].
Topics: Acute Disease; Age Factors; Amino Acid Metabolism, Inborn Errors; Child; Coma; Diagnosis, Differenti | 1989 |
[Kidney and central nervous system].
Topics: Blood-Brain Barrier; Coma; Creatinine; Guanidines; Humans; Kidney Failure, Chronic; Neurologic Manif | 1971 |
[Disorders of water-electrolyte metabolism associated with decompensated cirrhosis. The danger of various therapeutic drugs].
Topics: Acute Kidney Injury; Adult; Aged; Ascites; Blood Transfusion; Blood Urea Nitrogen; Blood Volume Dete | 1968 |
Ornithine transcarbamylase deficiency in the newborn infant.
Topics: Acidosis; Amino Acids; Ammonia; Autopsy; Blood Urea Nitrogen; Coma; Exchange Transfusion, Whole Bloo | 1973 |
Mortality in systemic lupus erythematosus: a 10-year review.
Topics: Adolescent; Adult; Aged; Bronchopneumonia; Cerebrospinal Fluid Proteins; Child; Chlorides; Coma; Cyc | 1973 |
Feeding the unconscious patient.
Topics: Aged; Blood Glucose; Body Weight; Coma; Dehydration; Enteral Nutrition; Female; Hematocrit; Humans; | 1971 |
Hyperammonemia due to a defect in hepatic ornithine transcarbamylase.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Central Nervous System Diseases; Child; Child | 1972 |
Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infant.
Topics: Ammonia; Chromatography, Gas; Coma; Humans; Infant; Infusions, Parenteral; Liver; Male; Metabolism, | 1972 |
Experience with urea in invert sugar for the treatment of cerebral malaria.
Topics: Brain Diseases; Child, Preschool; Coma; Encephalitis; Fructose; Glucose; Hemoglobinuria; Humans; Inf | 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 |
Biochemical changes after spontaneous subarachnoid hemorrhage. II. The patient on admission.
Topics: Adolescent; Adult; Aged; Aspartate Aminotransferases; Blood Cell Count; Blood Glucose; Blood Protein | 1966 |