ammonium hydroxide has been researched along with Cryptogenic Infantile Spasms in 5 studies
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 |
---|---|
Clothier, J; Ganapathy, V; Grooms, A; Kopel, J | 1 |
Sampath, S; Sivathanu, S; Sunderkumar, S; Veerasamy, M | 1 |
El-Chaar, GM; Raskind, JY | 1 |
Akanuma, Y; Kadowaki, H; Kadowaki, T; Kimura, S; Koda, N; Ogawa, Y; Yasuda, K | 1 |
Hanefeld, F | 1 |
1 review(s) available for ammonium hydroxide and Cryptogenic Infantile Spasms
Article | Year |
---|---|
The role of carnitine supplementation during valproic acid therapy.
Topics: Adolescent; Adult; Aged; Ammonia; Anticonvulsants; Carnitine; Chemical and Drug Induced Liver Injury; Child; Child, Preschool; Humans; Infant; Middle Aged; Myoclonus; Spasms, Infantile; Valproic Acid | 2000 |
4 other study(ies) available for ammonium hydroxide and Cryptogenic Infantile Spasms
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 Disorder; Citrates; Dicarboxylic Acid Transporters; Drosophila Proteins; Epilepsy; Female; Food Deprivation; Heterozygote; Humans; Lactates; Longevity; Metformin; Mice; Mutation, Missense; Point Mutation; Psychotic Disorders; Psychotropic Drugs; Pyruvates; Recurrence; Spasms, Infantile; Symporters; Tooth Abnormalities; Valproic Acid | 2021 |
Encephalopathy in an infant with infantile spasms: possible role of valproate toxicity.
Topics: Adrenocorticotropic Hormone; Ammonia; Anticonvulsants; Clonazepam; Drug Therapy, Combination; Female; Humans; Infant; Liver Function Tests; Neurotoxicity Syndromes; Spasms, Infantile; Valproic Acid | 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; Glutamate Dehydrogenase; Humans; Hyperinsulinism; Hypoglycemia; Infant, Newborn; Intellectual Disability; Japan; Male; Mutation, Missense; Pancreatectomy; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single-Stranded Conformational; Restriction Mapping; Spasms, Infantile | 2001 |
The clinical pattern of the Rett syndrome.
Topics: Adolescent; Adult; Ammonia; Ataxia; Child; Child Development; Child, Preschool; Dementia; Female; Follow-Up Studies; Humans; Infant; Intellectual Disability; Microcephaly; Neurocognitive Disorders; Spasms, Infantile; Stereotyped Behavior; Syndrome | 1985 |