ammonium hydroxide and Cryptogenic Infantile Spasms

ammonium hydroxide has been researched along with Cryptogenic Infantile Spasms in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's1 (20.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Clothier, J; Ganapathy, V; Grooms, A; Kopel, J1
Sampath, S; Sivathanu, S; Sunderkumar, S; Veerasamy, M1
El-Chaar, GM; Raskind, JY1
Akanuma, Y; Kadowaki, H; Kadowaki, T; Kimura, S; Koda, N; Ogawa, Y; Yasuda, K1
Hanefeld, F1

Reviews

1 review(s) available for ammonium hydroxide and Cryptogenic Infantile Spasms

ArticleYear
The role of carnitine supplementation during valproic acid therapy.
    The Annals of pharmacotherapy, 2000, Volume: 34, Issue:5

    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

Other Studies

4 other study(ies) available for ammonium hydroxide and Cryptogenic Infantile Spasms

ArticleYear
Metformin, valproic acid, and starvation induce seizures in a patient with partial SLC13A5 deficiency: a case of pharmaco-synergistic heterozygosity.
    Psychiatric genetics, 2021, 02-01, Volume: 31, Issue:1

    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.
    BMJ case reports, 2014, Apr-15, Volume: 2014

    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.
    Internal medicine (Tokyo, Japan), 2001, Volume: 40, Issue:1

    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.
    Brain & development, 1985, Volume: 7, Issue:3

    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