glycine has been researched along with Cryptogenic Infantile Spasms in 12 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| " The patient presented with myoclonic jerks, apnea and encephalopathy three months after birth without satisfactory therapeutic response." | 3.75 | Atypical glycine encephalopathy in an extremely low birth weight infant: description of a new mutation and clinical and electroencephalographic analysis. ( Carrascosa-Romero, MC; de Cabo-de la Vega, C; Gil-Pons, E; Iniesta-López, I; Martínez-Gutiérrez, A; Pardal-Fernández, JM, 2009) |
| "We report 3 cases of nonketotic hyperglycinemia, 2 typical neonatal and 1 atypical, diagnosed in Pediatric Hospital of Coimbra, Portugal, and investigated at Laboratory of Biochemical Genetics in 2004 to 2010 (incidence 1:47 455; prevalence 1:782 951)." | 1.39 | Nonketotic hyperglycinemia: a cause of encephalopathy in children. ( Diogo, L; Garcia, P; Grazina, M; Henriques, R; Robalo, C; Simões, M; Veríssimo, C, 2013) |
| " An adverse effect of high-dose serine therapy on head growth and on the transport of neutral amino acids across the blood-brain barrier should be considered and requires adjustment of treatment." | 1.31 | Phenotypic heterogeneity and adverse effects of serine treatment in 3-phosphoglycerate dehydrogenase deficiency: report on two siblings. ( Häusler, MG; Jaeken, J; Mönch, E; Ramaekers, VT, 2001) |
| "Glycine is a major inhibitory neurotransmitter in the CNS, but has also modulating effects at one of the glutamate receptors, the N-methyl-D-aspartate-(NMDA) receptor." | 1.29 | Ketamine and strychnine treatment of an infant with nonketotic hyperglycinaemia. ( Adams, HA; Günther, M; Heinemann, U; Roth, B; Sticht, G; Tegtmeyer-Metzdorf, H; Theisohn, M, 1995) |
| "The EEG changed to hypsarrhythmia during early or mid-infancy." | 1.26 | Nonketotic hyperglycinemia: electroencephalographic and evoked potential abnormalities. ( Brandt, IK; Garg, BP; Markand, ON, 1982) |
| "Strychnine treatment was initiated because it is a specific antagonist of glycine at postsynaptic membranes." | 1.26 | Strychnine therapy in nonketotic hyperglycinemia. ( Arneson, D; Ch'ien, LT; Chance, P; Wilroy, RS, 1979) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (50.00) | 18.7374 |
| 1990's | 2 (16.67) | 18.2507 |
| 2000's | 3 (25.00) | 29.6817 |
| 2010's | 1 (8.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Pardal-Fernández, JM | 1 |
| Carrascosa-Romero, MC | 1 |
| de Cabo-de la Vega, C | 1 |
| Iniesta-López, I | 1 |
| Gil-Pons, E | 1 |
| Martínez-Gutiérrez, A | 1 |
| Veríssimo, C | 1 |
| Garcia, P | 1 |
| Simões, M | 1 |
| Robalo, C | 1 |
| Henriques, R | 1 |
| Diogo, L | 1 |
| Grazina, M | 1 |
| Kaźmierczuk-Skubis, ME | 1 |
| Zatorska-Karpuś, M | 1 |
| Pac-Kozuchowska, E | 1 |
| Bojko-Jaworska, J | 1 |
| Furmaga-Jabłońska, W | 1 |
| Markand, ON | 1 |
| Garg, BP | 1 |
| Brandt, IK | 1 |
| Tegtmeyer-Metzdorf, H | 1 |
| Roth, B | 1 |
| Günther, M | 1 |
| Theisohn, M | 1 |
| Heinemann, U | 1 |
| Adams, HA | 1 |
| Sticht, G | 1 |
| de Koning, TJ | 1 |
| Poll-The, BT | 1 |
| Jaeken, J | 2 |
| Häusler, MG | 1 |
| Mönch, E | 1 |
| Ramaekers, VT | 1 |
| Arneson, D | 1 |
| Ch'ien, LT | 1 |
| Chance, P | 1 |
| Wilroy, RS | 1 |
| Meldrum, BS | 1 |
| Anlezark, G | 1 |
| Balzamo, E | 1 |
| Horton, RW | 1 |
| Trimble, M | 1 |
| Schiffmann, R | 1 |
| Kaye, EM | 1 |
| Willis, JK | 1 |
| Africk, D | 1 |
| Ampola, M | 1 |
| Terasaki, T | 1 |
| Yamatogi, Y | 1 |
| Ohtahara, S | 1 |
| Miyake, S | 1 |
| Iyoda, K | 1 |
| Narusawa, K | 1 |
| Seppäläinen, AM | 1 |
| Similä, S | 1 |
1 review available for glycine and Cryptogenic Infantile Spasms
| Article | Year |
|---|---|
Continuing education in neurometabolic disorders--serine deficiency disorders.
Topics: Adolescent; Amino Acids; Child; Deficiency Diseases; Female; Glycine; Humans; Ichthyosis; Male; Meta | 1999 |
11 other studies available for glycine and Cryptogenic Infantile Spasms
| Article | Year |
|---|---|
Atypical glycine encephalopathy in an extremely low birth weight infant: description of a new mutation and clinical and electroencephalographic analysis.
Topics: Aminomethyltransferase; Apnea; Brain; Brain Diseases, Metabolic; Electroencephalography; Fatal Outco | 2009 |
Nonketotic hyperglycinemia: a cause of encephalopathy in children.
Topics: Child; Female; Glycine; Humans; Hyperglycinemia, Nonketotic; Intellectual Disability; Lennox Gastaut | 2013 |
Non-ketotic hyperglycinemia as the cause of infant seizures--the case study.
Topics: Brain; Diagnosis, Differential; Electroencephalography; Female; Follow-Up Studies; Glycine; Humans; | 2004 |
Nonketotic hyperglycinemia: electroencephalographic and evoked potential abnormalities.
Topics: Amino Acid Metabolism, Inborn Errors; Brain Stem; Cerebral Cortex; Child, Preschool; Electroencephal | 1982 |
Ketamine and strychnine treatment of an infant with nonketotic hyperglycinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Chromosome Aberrations; Chromosome Disorders; Drug Therapy, Co | 1995 |
Phenotypic heterogeneity and adverse effects of serine treatment in 3-phosphoglycerate dehydrogenase deficiency: report on two siblings.
Topics: Amino Acids; Carbohydrate Dehydrogenases; Cerebrospinal Fluid; Child; Child, Preschool; Dose-Respons | 2001 |
Strychnine therapy in nonketotic hyperglycinemia.
Topics: Benzoates; Clonazepam; Drug Therapy, Combination; Electroencephalography; Enzymes; Female; Glycine; | 1979 |
Photically induced epilepsy in Papio papio as a model for drug studies.
Topics: Acetylcholine; Animals; Carbamazepine; Clonazepam; Diazepam; Disease Models, Animal; Dopamine; Dose- | 1975 |
Transient neonatal hyperglycinemia.
Topics: Amino Acid Metabolism, Inborn Errors; Blood Glucose; Female; Follow-Up Studies; Genes, Recessive; Gl | 1989 |
[A long-term follow-up study on a case with glycine encephalopathy].
Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Child, Preschool; Diazepam; Electro | 1988 |
Electroencephalographic findings in three patients with nonketotic hyperglycinemia.
Topics: Amino Acid Metabolism, Inborn Errors; Electroencephalography; Glycine; Humans; Infant; Infant, Newbo | 1971 |