ammonium hydroxide has been researched along with Spasms, Infantile in 5 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Spasms, Infantile: An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Carnitine is an essential amino acid necessary in beta-oxidation of fatty acids and energy production in cellular mitochondria." | 2.41 | The role of carnitine supplementation during valproic acid therapy. ( El-Chaar, GM; Raskind, JY, 2000) |
| " However, a complete reversal of encephalopathy, on withdrawal of the drug, strongly suggested an adverse drug reaction (ADR) due to valproic acid." | 1.40 | Encephalopathy in an infant with infantile spasms: possible role of valproate toxicity. ( Sampath, S; Sivathanu, S; Sunderkumar, S; Veerasamy, M, 2014) |
| "A boy suffered from hypoglycemic coma with relative hyperinsulinemia on day 1 after birth, and received subtotal pancreatectomy." | 1.31 | A Japanese case of congenital hyperinsulinism with hyperammonemia due to a mutation in glutamate dehydrogenase (GLUD1) gene. ( Akanuma, Y; Kadowaki, H; Kadowaki, T; Kimura, S; Koda, N; Ogawa, Y; Yasuda, K, 2001) |
| "Rett syndrome was also observed in two sisters." | 1.27 | The clinical pattern of the Rett syndrome. ( Hanefeld, F, 1985) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kopel, J | 1 |
| Grooms, A | 1 |
| Ganapathy, V | 1 |
| Clothier, J | 1 |
| Sivathanu, S | 1 |
| Sampath, S | 1 |
| Veerasamy, M | 1 |
| Sunderkumar, S | 1 |
| Raskind, JY | 1 |
| El-Chaar, GM | 1 |
| Yasuda, K | 1 |
| Koda, N | 1 |
| Kadowaki, H | 1 |
| Ogawa, Y | 1 |
| Kimura, S | 1 |
| Kadowaki, T | 1 |
| Akanuma, Y | 1 |
| Hanefeld, F | 1 |
1 review available for ammonium hydroxide and Spasms, Infantile
| Article | Year |
|---|---|
The role of carnitine supplementation during valproic acid therapy.
Topics: Adolescent; Adult; Aged; Ammonia; Anticonvulsants; Carnitine; Chemical and Drug Induced Liver Injury | 2000 |
4 other studies available for ammonium hydroxide and Spasms, Infantile
| Article | Year |
|---|---|
Metformin, valproic acid, and starvation induce seizures in a patient with partial SLC13A5 deficiency: a case of pharmaco-synergistic heterozygosity.
Topics: Adult; Amino Acid Substitution; Ammonia; Animals; Anticonvulsants; Autistic Disorder; Bipolar Disord | 2021 |
Encephalopathy in an infant with infantile spasms: possible role of valproate toxicity.
Topics: Adrenocorticotropic Hormone; Ammonia; Anticonvulsants; Clonazepam; Drug Therapy, Combination; Female | 2014 |
A Japanese case of congenital hyperinsulinism with hyperammonemia due to a mutation in glutamate dehydrogenase (GLUD1) gene.
Topics: Allosteric Regulation; Amino Acid Substitution; Ammonia; Apnea; Coma; Genetic Heterogeneity; Glutama | 2001 |
The clinical pattern of the Rett syndrome.
Topics: Adolescent; Adult; Ammonia; Ataxia; Child; Child Development; Child, Preschool; Dementia; Female; Fo | 1985 |