glycine has been researched along with Acquired Metabolic Diseases, Brain in 25 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "0% mannitol distention fluid produces greater postoperative dilutional hyponatremia than 1." | 5.08 | Preventing hyponatremic encephalopathy: comparison of serum sodium and osmolality during operative hysteroscopy with 5.0% mannitol and 1.5% glycine distention media. ( Haselkorn, JS; Milim, SJ; Nathanson, HG; Phillips, DR; Phillips, RE, 1997) |
| " 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) |
| "Coma and convulsions develop in neonates in typical GE while psychomotor retardation and behavioral abnormalities in infancy and childhood are observed in mild GE." | 1.35 | Model mice for mild-form glycine encephalopathy: behavioral and biochemical characterizations and efficacy of antagonists for the glycine binding site of N-methyl D-aspartate receptor. ( Aoki, Y; Ichinohe, A; Kamada, F; Kanno, J; Kojima-ishii, K; Komatsuzaki, S; Kure, S; Matsubara, Y; Mizoi, K; Nakahara, D; Narisawa, A; Oda, M; Shinka, T; Sugawara, T; Yokoyama, H, 2008) |
| "Late-onset nonketotic hyperglycinemia is very rare, presents with varied clinical features, and may be underdiagnosed." | 1.34 | Late-onset nonketotic hyperglycinemia with leukodystrophy and an unusual clinical course. ( Carpenter, K; Chiong, MA; Procopis, P; Wilcken, B, 2007) |
| "Glycine content was elevated 2- to 8-fold and glycine cleavage enzyme activity was undetectable in the brains of the glycine encephalopathy patients." | 1.26 | Studies of the glycine cleavage enzyme system in brain from infants with glycine encephalopathy. ( Hansen, S; Perry, TL; Urquhart, N, 1977) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 9 (36.00) | 18.7374 |
| 1990's | 5 (20.00) | 18.2507 |
| 2000's | 7 (28.00) | 29.6817 |
| 2010's | 4 (16.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ostojic, SM | 1 |
| Schulze, A | 1 |
| Battini, R | 1 |
| 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 |
| Kolling, J | 1 |
| Wyse, AT | 2 |
| Popek, M | 1 |
| Walter, M | 1 |
| Fernando, M | 1 |
| Lindner, M | 1 |
| Schwab, KO | 1 |
| Sass, JO | 1 |
| Netto, CA | 1 |
| Barker, C | 1 |
| Jefferson, P | 1 |
| Ball, DR | 1 |
| Chiong, MA | 1 |
| Procopis, P | 1 |
| Carpenter, K | 1 |
| Wilcken, B | 1 |
| Kojima-ishii, K | 1 |
| Kure, S | 1 |
| Ichinohe, A | 1 |
| Shinka, T | 1 |
| Narisawa, A | 1 |
| Komatsuzaki, S | 1 |
| Kanno, J | 1 |
| Kamada, F | 1 |
| Aoki, Y | 1 |
| Yokoyama, H | 1 |
| Oda, M | 1 |
| Sugawara, T | 1 |
| Mizoi, K | 1 |
| Nakahara, D | 1 |
| Matsubara, Y | 1 |
| Agamanolis, DP | 1 |
| Potter, JL | 1 |
| Herrick, MK | 1 |
| Sternberger, NH | 1 |
| Mendelson, IS | 1 |
| Sankaran, K | 1 |
| Casey, RE | 1 |
| Zaleski, WA | 1 |
| Mendelson, IM | 1 |
| Hitta, P | 1 |
| Bertaud, N | 1 |
| Tada, K | 1 |
| Ponsot, G | 1 |
| Boneh, A | 1 |
| Degani, Y | 1 |
| Harari, M | 1 |
| Phillips, DR | 1 |
| Milim, SJ | 1 |
| Nathanson, HG | 1 |
| Phillips, RE | 1 |
| Haselkorn, JS | 1 |
| van der Knaap, MS | 1 |
| Verhoeven, NM | 1 |
| Maaswinkel-Mooij, P | 1 |
| Pouwels, PJ | 1 |
| Onkenhout, W | 1 |
| Peeters, EA | 1 |
| Stöckler-Ipsiroglu, S | 1 |
| Jakobs, C | 1 |
| Gabis, L | 1 |
| Parton, P | 1 |
| Roche, P | 1 |
| Lenn, N | 1 |
| Tudorica, A | 1 |
| Huang, W | 1 |
| Perry, TL | 2 |
| Urquhart, N | 1 |
| Hansen, S | 1 |
| Kish, SJ | 1 |
| Dixon, LM | 1 |
| Burnham, WM | 1 |
| Becker, L | 1 |
| Cheng, J | 1 |
| Chang, LJ | 1 |
| Rebbetoy, M | 1 |
| Terasaki, T | 1 |
| Yamatogi, Y | 1 |
| Ohtahara, S | 1 |
| Miyake, S | 1 |
| Iyoda, K | 1 |
| Narusawa, K | 1 |
| Sperl, W | 1 |
| Parth, J | 1 |
| Rumpl, E | 1 |
| Haffner, B | 1 |
| Holmqvist, P | 1 |
| Polberger, S | 1 |
4 reviews available for glycine and Acquired Metabolic Diseases, Brain
| Article | Year |
|---|---|
Pre-symptomatic treatment of creatine biosynthesis defects.
Topics: Amidinotransferases; Brain Diseases, Metabolic; Creatine; Glycine; Guanidinoacetate N-Methyltransfer | 2007 |
Behavioral and neurochemical effects of proline.
Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Animals; Antioxidants | 2011 |
[Molecular lesion and pathophysiology of hyperglycinemia (glycine encephalopathy)].
Topics: Amino Acid Oxidoreductases; Amino Acid Sequence; Animals; Brain; Brain Diseases, Metabolic; Carrier | 1993 |
[Hyperglycinemia without ketosis and NMDA receptor dysfunction].
Topics: Brain Diseases, Metabolic; Glycine; Humans; Receptors, N-Methyl-D-Aspartate | 1996 |
1 trial available for glycine and Acquired Metabolic Diseases, Brain
| Article | Year |
|---|---|
Preventing hyponatremic encephalopathy: comparison of serum sodium and osmolality during operative hysteroscopy with 5.0% mannitol and 1.5% glycine distention media.
Topics: Adult; Brain Diseases, Metabolic; Female; Follow-Up Studies; Glycine; Humans; Hyponatremia; Hysteros | 1997 |
20 other studies available for glycine and Acquired Metabolic Diseases, Brain
| Article | Year |
|---|---|
A new perspective to improve brain bioenergetics in disorders with functional GAMT and CT1.
Topics: Animals; Brain; Brain Diseases, Metabolic; Creatine; Energy Metabolism; Glycine; Guanidinoacetate N- | 2016 |
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 |
Creatine prevents the inhibition of energy metabolism and lipid peroxidation in rats subjected to GAA administration.
Topics: Animals; Brain Diseases, Metabolic; Creatine; Disease Models, Animal; Energy Metabolism; Glycine; Gu | 2010 |
Two inborn errors of metabolism in a newborn: glutaric aciduria type I combined with isobutyrylglycinuria.
Topics: Amino Acid Metabolism, Inborn Errors; Base Sequence; Brain Diseases, Metabolic; DNA Mutational Analy | 2010 |
Glycine encephalopathy and anesthesia.
Topics: Anesthesia; Anesthesia Recovery Period; Brain Diseases, Metabolic; Child; Glycine; Humans; Methyl Et | 2007 |
Late-onset nonketotic hyperglycinemia with leukodystrophy and an unusual clinical course.
Topics: Age of Onset; Brain Diseases, Metabolic; Cerebral Palsy; Child, Preschool; Female; Gait; Glycine; Hu | 2007 |
Model mice for mild-form glycine encephalopathy: behavioral and biochemical characterizations and efficacy of antagonists for the glycine binding site of N-methyl D-aspartate receptor.
Topics: Aggression; Amino Acid Oxidoreductases; Animals; Anxiety; Binding Sites; Brain Diseases, Metabolic; | 2008 |
The neuropathology of glycine encephalopathy: a report of five cases with immunohistochemical and ultrastructural observations.
Topics: Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases, Metabolic; Female; Glial Fibrillary Aci | 1982 |
Prenatal diagnosis of glycine encephalopathy.
Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Brain Diseases, Metabolic; Female; Glycine; Hu | 1982 |
A strategy for glycine encephalopathy therapy.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Oxidoreductases; Aminomethyltransferase; Animals; B | 1982 |
Glycine encephalopathy in a neonate. Treatment with intravenous strychnine and sodium benzoate.
Topics: Amino Acid Metabolism, Inborn Errors; Benzoates; Brain Diseases, Metabolic; Exchange Transfusion, Wh | 1982 |
[Severe neurologic disorders after surgical hysteroscopy with glycol irrigation].
Topics: Adult; Brain Diseases, Metabolic; Female; Glycine; Humans; Hyponatremia; Hysteroscopy; Therapeutic I | 1993 |
Prognostic clues and outcome of early treatment of nonketotic hyperglycinemia.
Topics: Amino Acid Metabolism, Inborn Errors; Benzoates; Benzoic Acid; Brain Diseases, Metabolic; Child, Pre | 1996 |
Mental retardation and behavioral problems as presenting signs of a creatine synthesis defect.
Topics: Aspartic Acid; Body Fluids; Brain Diseases, Metabolic; Child, Preschool; Creatine; Diagnosis, Differ | 2000 |
In vivo 1H magnetic resonance spectroscopic measurement of brain glycine levels in nonketotic hyperglycinemia.
Topics: Aspartic Acid; Brain; Brain Diseases, Metabolic; Choline; Chromosome Aberrations; Chromosome Disorde | 2001 |
Studies of the glycine cleavage enzyme system in brain from infants with glycine encephalopathy.
Topics: Amino Acid Metabolism, Inborn Errors; Arthrobacter; Bicarbonates; Brain; Brain Diseases, Metabolic; | 1977 |
Brain neurotransmitters in glycine encephalopathy.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Brain Diseases, Metabolic; Cerebral Cortex; Glyci | 1988 |
[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 |
[Glycine encephalopathy: a non-ketotic disorder of glycine catabolism].
Topics: Brain; Brain Diseases, Metabolic; Electroencephalography; Evoked Potentials, Somatosensory; Glycine; | 1985 |
Neonatal non-ketotic hyperglycinemia (NKH). Diagnoses and management in two cases.
Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Cerebral Hemorrhage; Female; Follow | 1985 |