ammonium hydroxide has been researched along with Emesis in 27 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Citrullinemia type I (CTLN1) is a urea cycle disorder which typically presents in the neonatal period or infancy with hyperammonemia and concurrent neurologic deterioration." | 7.77 | Transient fulminant liver failure as an initial presentation in citrullinemia type I. ( Baruteau, J; de Baulny, HO; Faghfoury, H; Häberle, J; Schulze, A, 2011) |
| "Citrullinemia type I (CTLN1) is a urea cycle disorder which typically presents in the neonatal period or infancy with hyperammonemia and concurrent neurologic deterioration." | 3.77 | Transient fulminant liver failure as an initial presentation in citrullinemia type I. ( Baruteau, J; de Baulny, HO; Faghfoury, H; Häberle, J; Schulze, A, 2011) |
| " 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 an X-linked disorder which results in the accumulation of ammonia causing irritability and vomiting." | 1.91 | Acute onset of ornithine transcarbamylase deficiency after total anomalous pulmonary venous connection repair to a 2-day-old neonate. ( Fuchigami, T; Iwata, Y; Katagiri, J; Yoshida, H, 2023) |
| "She was diagnosed with ornithine transcarbamylase deficiency (OTCD) by analyses of plasma amino acids, urinary orotic acid, and the OTC gene mutation." | 1.51 | Hyperammonemia in a Woman with Late-onset Ornithine Transcarbamylase Deficiency. ( Harada, M; Hiura, M; Honma, Y; Ishii, M; Koya, Y; Matsumoto, S; Senju, M; Shibata, M, 2019) |
| "Non-neurologic complications included respiratory failure (14 patients, 31." | 1.43 | Initial Serum Ammonia as a Predictor of Neurologic Complications in Patients with Acute Glufosinate Poisoning. ( Cha, K; Cha, YS; Go, J; Hwang, SO; Kim, H; Kim, OH; Kim, TH; Lee, DK; Lee, KH; Youk, H, 2016) |
| "Late-onset OTC deficiency has been described in patients of all ages." | 1.29 | Vomiting, ataxia, and altered mental status in an adolescent: late-onset ornithine transcarbamylase deficiency. ( Myers, JH; Shook, JE, 1996) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 18 (66.67) | 18.7374 |
| 1990's | 2 (7.41) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 6 (22.22) | 24.3611 |
| 2020's | 1 (3.70) | 2.80 |
| Authors | Studies |
|---|---|
| Yoshida, H | 1 |
| Iwata, Y | 1 |
| Fuchigami, T | 1 |
| Katagiri, J | 1 |
| Bennett, EE | 1 |
| Hummel, K | 1 |
| Smith, AG | 1 |
| Longo, N | 1 |
| Koya, Y | 1 |
| Shibata, M | 1 |
| Senju, M | 1 |
| Honma, Y | 1 |
| Hiura, M | 1 |
| Ishii, M | 1 |
| Matsumoto, S | 1 |
| Harada, M | 1 |
| Zwickler, T | 1 |
| Riderer, A | 1 |
| Haege, G | 1 |
| Hoffmann, GF | 1 |
| Kölker, S | 1 |
| Burgard, P | 1 |
| Lee, DK | 1 |
| Youk, H | 1 |
| Kim, H | 1 |
| Kim, OH | 1 |
| Go, J | 1 |
| Kim, TH | 1 |
| Cha, K | 1 |
| Lee, KH | 1 |
| Hwang, SO | 1 |
| Cha, YS | 1 |
| Faghfoury, H | 1 |
| Baruteau, J | 1 |
| de Baulny, HO | 1 |
| Häberle, J | 1 |
| Schulze, A | 1 |
| Hashash, JG | 1 |
| Thudi, K | 1 |
| Malik, SM | 1 |
| TOKITA, K | 1 |
| KAWAMURA, H | 1 |
| OMOTO, M | 1 |
| YASHIKI, S | 1 |
| OTSUKI, T | 1 |
| EBISAWA, K | 1 |
| NAKAMURA, U | 1 |
| IWANAGA, Y | 1 |
| YONEMITSU, S | 1 |
| TAGUCHI, M | 1 |
| ISHIKAWA, E | 1 |
| Czarnecki, GL | 1 |
| Baker, DH | 2 |
| Myers, JH | 1 |
| Shook, JE | 1 |
| Plecko, B | 1 |
| Erwa, W | 1 |
| Wermuth, B | 1 |
| Anderson, PA | 1 |
| Corbin, JE | 1 |
| Morris, JG | 1 |
| Rogers, QR | 1 |
| Drogari, E | 1 |
| Leonard, JV | 1 |
| Rowe, PC | 1 |
| Newman, SL | 1 |
| Brusilow, SW | 1 |
| Farriaux, JP | 1 |
| Dhondt, JL | 1 |
| Cathelineau, L | 1 |
| Ratel, J | 1 |
| Fontaine, G | 1 |
| Kodama, J | 1 |
| Higashino, K | 1 |
| Kobayashi, S | 1 |
| Izumi, K | 1 |
| Satani, M | 1 |
| Seldin, DW | 1 |
| Rector, FC | 1 |
| Kaye, CI | 1 |
| Morrow, G | 1 |
| Nadler, HL | 1 |
| MacLeod, P | 1 |
| Mackenzie, S | 1 |
| Scriver, CR | 1 |
| Corbeel, LM | 1 |
| Colombo, JP | 1 |
| Van Sande, M | 1 |
| Weber, A | 1 |
| Chow, KW | 1 |
| Pond, WG | 1 |
| Walker, EF | 1 |
| Freeman, JM | 1 |
| Nicholson, JF | 1 |
| Schimke, RT | 1 |
| Rowland, LP | 1 |
| Carter, S | 1 |
| Levin, B | 2 |
| Abraham, JM | 1 |
| Oberholzer, VG | 1 |
| Burgess, EA | 2 |
| Dobbs, RH | 1 |
| Palmer, T | 1 |
| Huttenlocher, PR | 1 |
| Schwartz, AD | 1 |
| Klatskin, G | 1 |
| Bauer, HJ | 1 |
1 review available for ammonium hydroxide and Emesis
| Article | Year |
|---|---|
Symposium on acid-base homeostasis. The generation and maintenance of metabolic alkalosis.
Topics: Alkalosis; Ammonia; Animals; Bicarbonates; Diarrhea; Diet, Sodium-Restricted; Diuretics; Extracellul | 1972 |
26 other studies available for ammonium hydroxide and Emesis
| Article | Year |
|---|---|
Acute onset of ornithine transcarbamylase deficiency after total anomalous pulmonary venous connection repair to a 2-day-old neonate.
Topics: Ammonia; Humans; Hyperammonemia; Infant, Newborn; Male; Ornithine Carbamoyltransferase Deficiency Di | 2023 |
Acute Presentation and Management of the Encephalopathic Child With an Undiagnosed Inborn Error of Metabolism.
Topics: Ammonia; Brain Diseases; Child; Delayed Diagnosis; Delirium; Emergency Service, Hospital; Humans; Hy | 2019 |
Hyperammonemia in a Woman with Late-onset Ornithine Transcarbamylase Deficiency.
Topics: Adolescent; Amino Acids; Ammonia; Arginine; Coma; Female; Humans; Hyperammonemia; Male; Middle Aged; | 2019 |
Usefulness of biochemical parameters in decision-making on the start of emergency treatment in patients with propionic acidemia.
Topics: Acid-Base Equilibrium; Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Appetite; C | 2014 |
Initial Serum Ammonia as a Predictor of Neurologic Complications in Patients with Acute Glufosinate Poisoning.
Topics: Adult; Aged; Aged, 80 and over; Aminobutyrates; Ammonia; Emergency Service, Hospital; Female; Glasgo | 2016 |
Transient fulminant liver failure as an initial presentation in citrullinemia type I.
Topics: Ammonia; Argininosuccinate Synthase; Base Sequence; Citrulline; Citrullinemia; Fatty Liver; Female; | 2011 |
An 18-year-old woman with a 15-cm liver mass and an ammonia level of 342.
Topics: Adolescent; Ammonia; Carcinoma, Hepatocellular; Confusion; Female; Humans; Liver Neoplasms; Lung Neo | 2012 |
[REGULATION MECHANISM OF THE AUTONOMIC NERVOUS FUNCTIONS. (XXIV) ON THE FUNCTION OF THE NERVUS LARYNIGICUS CRANIALIS INTERNA (N. 1. CR. INT.)].
Topics: Amines; Ammonia; Animals; Copper; Dogs; Electric Stimulation; Esophagus; Intestine, Large; Intestine | 1964 |
Urea cycle function in the dog with emphasis on the role of arginine.
Topics: Age Factors; Ammonia; Animals; Arginine; Blood Glucose; Citrulline; Dogs; Ornithine; Orotic Acid; Ur | 1984 |
Vomiting, ataxia, and altered mental status in an adolescent: late-onset ornithine transcarbamylase deficiency.
Topics: Adolescent; Age of Onset; Amino Acid Metabolism, Inborn Errors; Ammonia; Ataxia; Cognition Disorders | 1996 |
Partial N-acetylglutamate synthetase deficiency in a 13-year-old girl: diagnosis and response to treatment with N-carbamylglutamate.
Topics: Acetyltransferases; Adolescent; Amino-Acid N-Acetyltransferase; Ammonia; Female; Glutamates; Humans; | 1998 |
Lysine and arginine requirements of the domestic cat.
Topics: Ammonia; Animals; Arginine; Body Weight; Cats; Female; Lysine; Male; Nutritional Requirements; Vomit | 1979 |
Arginine: an essential amino acid for the cat.
Topics: Ammonia; Animal Nutritional Physiological Phenomena; Animals; Arginine; Cats; Hyperglycemia; Male; N | 1978 |
Late onset ornithine carbamoyl transferase deficiency in males.
Topics: Adolescent; Age Factors; Ammonia; Child; Child, Preschool; Genetic Linkage; Heterozygote; Humans; In | 1988 |
Natural history of symptomatic partial ornithine transcarbamylase deficiency.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Ataxia; Child, Preschool; Coma; Diagnosis, Differenti | 1986 |
Hyperammonemia through deficiency of ornithine carbamyl transferase.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Dietary Proteins; Humans; Infant; Male; | 1974 |
[Developing mechanism of the adverse effects of L-asparaginase and their control].
Topics: Ammonia; Arginine; Asparaginase; Glutamates; Humans; Injections, Intravenous; Leukemia, Myeloid, Acu | 1974 |
In vitro "responsive" methylmalonic acidemia: a new variant.
Topics: Amino Acids; Ammonia; Carbon Dioxide; Carbon Radioisotopes; Cells, Cultured; Child, Preschool; Cobam | 1974 |
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 |
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 |
Blood metabolites in the hyperammonemic pig.
Topics: Ammonia; Animals; Auditory Perception; Blood Glucose; Calcium; Carbonates; Citric Acid Cycle; Hyperv | 1970 |
Congenital hyperammonemia. Association with hyperglycinemia and decreased levels of carbamyl phosphate synthetase.
Topics: Amino Acids; Ammonia; Citric Acid Cycle; Female; Glycine; Humans; Infant, Newborn; Metabolism, Inbor | 1970 |
Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.
Topics: Adult; Amino Acids; Ammonia; Ammonium Chloride; Citrates; Citric Acid Cycle; Diet Therapy; Dietary P | 1969 |
Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase.
Topics: Alanine; Amino Acids; Ammonia; Arginine; Citrates; Citric Acid Cycle; Diet Therapy; Dietary Proteins | 1969 |
Reye's syndrome: ammonia intoxication as a possible factor in the encephalopathy.
Topics: Adolescent; Ammonia; Brain Diseases; Child; Child, Preschool; Coma; Dermatitis; Fatty Liver; Female; | 1969 |
[Symptoms of encephalopathies from the viewpoint of the neurologist].
Topics: Ammonia; Brain; Electroencephalography; Headache; Hepatic Encephalopathy; Humans; Neurologic Manifes | 1966 |