glycine has been researched along with Acetonemia in 30 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Therapy with benzoic acid in a case of classic neonatal non-ketotic hyperglycinaemia (NKH) was successful in stopping seizures but not in promoting mental development." | 3.69 | Response to sodium benzoate treatment in non-ketotic hyperglycinaemia. ( Hobusch, D; Krüger, G; Radke, M; Stolpe, HJ; Tittelbach-Helmrich, W; Uhlemann, M; Walther, F, 1994) |
| "The patient was lethargic." | 1.37 | Beta-ketothiolase deficiency brought with lethargy: case report. ( Arica, SG; Arica, V; Dag, H; Gülbayzar, S; Obut, O; Onur, H, 2011) |
| "Dextromethorphan was added to the regimen on day 12." | 1.28 | Dextromethorphan and high-dose benzoate therapy for nonketotic hyperglycinemia in an infant. ( Francomano, CA; Hamosh, A; Johnston, MV; McDonald, JW; Niedermeyer, E; Valle, D, 1992) |
| "Both patients had episodic ketosis and metabolic acidosis." | 1.27 | 3-Ketothiolase deficiency. ( Bartlett, K; Cannon, RA; Conde, C; Gomez Vazquez, J; Lipson, M; Middleton, B; Nyhan, WL; Romanos, A; Sweetman, L, 1986) |
| "However, ketonuria was not a consistent part of his clinical picture, and he had at least two episodes of acute overwhelming illness, the latter one fatal, in which ketones were never found in the urine." | 1.25 | Hyperglycinemia and propionyl coA carboxylase deficiency and episodic severe illness without consistent ketosis. ( Ando, T; Kilroy, A; Nyhan, WL; Sweetman, L; Wadlington, WB, 1975) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 22 (73.33) | 18.7374 |
| 1990's | 5 (16.67) | 18.2507 |
| 2000's | 2 (6.67) | 29.6817 |
| 2010's | 1 (3.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Arica, V | 1 |
| Arica, SG | 1 |
| Dag, H | 1 |
| Onur, H | 1 |
| Obut, O | 1 |
| Gülbayzar, S | 1 |
| SAUER, F | 1 |
| Hayasaka, K | 4 |
| Tada, K | 4 |
| Kikuchi, G | 1 |
| Winter, S | 1 |
| Nyhan, WL | 3 |
| Schoos-Barbette, S | 1 |
| Gerard, J | 1 |
| Francotte, N | 1 |
| Lambotte, C | 1 |
| Del Valle, JA | 1 |
| Merinero, B | 2 |
| Garciá, MJ | 2 |
| Ugarte, M | 2 |
| Omeñaca, F | 1 |
| Neustadt, G | 1 |
| DelValle, JA | 1 |
| Jiménez, A | 1 |
| Solaguren, R | 1 |
| López, O | 1 |
| Condado, I | 1 |
| Narisawa, K | 1 |
| Satoh, T | 1 |
| Tateda, H | 1 |
| Metoki, K | 1 |
| Hiraga, K | 1 |
| Aoki, T | 1 |
| Kawakami, T | 1 |
| Akamatsu, H | 1 |
| Matsuo, N | 1 |
| Gerbasi, F | 1 |
| Scotto, E | 1 |
| Gueci, G | 1 |
| Harris, DJ | 1 |
| Thompson, RM | 1 |
| Wolf, B | 1 |
| Yang, BI | 1 |
| Walther, F | 1 |
| Radke, M | 1 |
| Krüger, G | 1 |
| Hobusch, D | 1 |
| Uhlemann, M | 1 |
| Tittelbach-Helmrich, W | 1 |
| Stolpe, HJ | 1 |
| Tanaka, Y | 1 |
| Miyazaki, M | 1 |
| Tsuda, M | 1 |
| Murai, K | 1 |
| Kuzuhara, S | 1 |
| Schmitt, B | 1 |
| Steinmann, B | 1 |
| Thio, LL | 1 |
| Wong, M | 1 |
| Yamada, KA | 1 |
| Toone, JR | 1 |
| Applegarth, DA | 1 |
| Coulter-Mackie, MB | 1 |
| James, ER | 1 |
| Baumgartner, ER | 1 |
| Bachmann, C | 1 |
| Brechbühler, T | 1 |
| Wick, H | 1 |
| Shuman, RM | 1 |
| Leech, RW | 1 |
| Scott, CR | 1 |
| Hyánek, J | 1 |
| Pospisil, R | 1 |
| Hoza, J | 1 |
| Mechlová, V | 1 |
| Novotná, J | 1 |
| Kapras, J | 1 |
| Podhradska, O | 1 |
| Kopejtková, H | 1 |
| Tauchmanová, H | 1 |
| Viletová, H | 1 |
| Kunová, V | 1 |
| O'Brien, WE | 1 |
| de Groot, CJ | 1 |
| Boeli Everts, V | 1 |
| Touwen, BC | 1 |
| Hommes, FA | 1 |
| Branski, D | 1 |
| Gale, R | 1 |
| Gross-Kieselstein, E | 1 |
| Abrahamov, A | 1 |
| Kelly, S | 1 |
| Leikhim, E | 1 |
| Wadlington, WB | 1 |
| Kilroy, A | 1 |
| Ando, T | 1 |
| Sweetman, L | 2 |
| Rowley, BO | 1 |
| Brothers, V | 1 |
| Gerritsen, T | 1 |
| Krieger, I | 1 |
| Tanaka, K | 1 |
| Elleau, C | 1 |
| Parrot-Roulaud, F | 1 |
| Perel, Y | 1 |
| Divry, P | 1 |
| Rolland, MO | 1 |
| Zabot, MT | 1 |
| Middleton, R | 1 |
| Guillard, JM | 1 |
| Hamosh, A | 1 |
| McDonald, JW | 1 |
| Valle, D | 2 |
| Francomano, CA | 1 |
| Niedermeyer, E | 1 |
| Johnston, MV | 1 |
| Singer, HS | 1 |
| Leonard, JV | 1 |
| Middleton, B | 2 |
| Seakins, JW | 1 |
| Bartlett, K | 1 |
| Romanos, A | 1 |
| Gomez Vazquez, J | 1 |
| Conde, C | 1 |
| Cannon, RA | 1 |
| Lipson, M | 1 |
1 review available for glycine and Acetonemia
| Article | Year |
|---|---|
Non-ketotic hyperglycinaemia: clinical and biochemical aspects.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Oxidoreductases; Brain; Carrier Proteins; Diagnosis | 1987 |
29 other studies available for glycine and Acetonemia
| Article | Year |
|---|---|
Beta-ketothiolase deficiency brought with lethargy: case report.
Topics: 3-Hydroxybutyric Acid; Acetyl-CoA C-Acyltransferase; Amino Acid Metabolism, Inborn Errors; Carnitine | 2011 |
Acetoacetate and beta-hydroxy-beta-methyl glutaryl coenzyme A metabolism in normal and ketotic guinea pigs.
Topics: Acetoacetates; Acidosis; Acyl Coenzyme A; Coenzymes; Glycine; Guinea Pigs; Ketoses; Ketosis | 1961 |
Nonketotic hyperglycinemia: two patients with primary defects of P-protein and T-protein, respectively, in the glycine cleavage system.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Oxidoreductases; Aminomethyltransferase; Brain; Car | 1983 |
A treatment of non-ketotic hyperglycinaemia.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Combined Modality Therapy; Deoxych | 1984 |
Leukocyte propionyl-CoA carboxylase deficiency in a patient with ketotic hyperglycinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Carbon-Carbon Ligases; Female; Glycine; Humans; Infant, Newbor | 1980 |
Late onset type of propionic acidaemia: case report and biochemical studies.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Carbon-Carbon Ligases; Female; Glycine; Humans; Hydr | 1981 |
Glycine cleavage system in ketotic hyperglycinemia: a reduction of H-protein activity.
Topics: Acidosis; Amino Acid Oxidoreductases; Carrier Proteins; Female; Glycine; Glycine Decarboxylase Compl | 1982 |
[Ketotic hyperglycinemic syndrome].
Topics: Agammaglobulinemia; Amino Acid Metabolism, Inborn Errors; Female; Glycine; Humans; Infant; Ketosis; | 1982 |
Propionyl coenzyme A carboxylase deficiency presenting as non-ketotic hyperglycinaemia.
Topics: Carboxy-Lyases; Female; Glycine; Humans; Infant; Ketosis; Methylmalonyl-CoA Decarboxylase; Myoclonus | 1981 |
Response to sodium benzoate treatment in non-ketotic hyperglycinaemia.
Topics: Benzoates; Benzoic Acid; Dose-Response Relationship, Drug; Female; Glycine; Humans; Infant, Newborn; | 1994 |
Blindness due to non-ketotic hyperglycinemia: report of a 38-year-old, the oldest case to date.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Blindness; Female; Glycine; Humans; Ketosis; Optic Atro | 1993 |
Dextromethorphan in infantile nonketotic hyperglycinemia.
Topics: Dextromethorphan; Dextrorphan; Glycine; Humans; Infant; Ketosis; Receptors, N-Methyl-D-Aspartate; Se | 1993 |
Ketone bodies do not directly alter excitatory or inhibitory hippocampal synaptic transmission.
Topics: 3-Hydroxybutyric Acid; 4-Aminopyridine; Acetoacetates; Animals; Cells, Cultured; Diet; Entorhinal Co | 2000 |
Recurrent mutations in P- and T-proteins of the glycine cleavage complex and a novel T-protein mutation (N145I): a strategy for the molecular investigation of patients with nonketotic hyperglycinemia (NKH).
Topics: Amino Acid Oxidoreductases; Aminomethyltransferase; DNA Primers; Exons; Gene Frequency; Glycine; Gly | 2001 |
Acute neonatal nonketotic hyperglycinemia: normal propionate and methylmalonate metabolism.
Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Coenzyme A; Female; Fi | 1975 |
The neuropathology of the nonketotic and ketotic hyperglycinemias: three cases.
Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Corpus Callosum; Demyelinating Diseases; Fem | 1978 |
Hyperglycinaemia without ketosis.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Child, Preschool; Glycine; Humans; Ketosis; Male | 1977 |
Inhibition of glycine synthase by branched-chain alpha-keto acids. A possible mechanism for abnormal glycine metabolism in ketotic hyperglycinemia.
Topics: Acidosis; Acyl Coenzyme A; Animals; Caproates; Glycine; Keto Acids; Ketosis; Liver; Male; Rats; Tran | 1978 |
Non-ketotic hyperglycinemia (NKH): an inborn error of metabolism affecting brain function exclusively.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Behavior, Animal; Glycine; Humans; Intellectual Disab | 1978 |
Propionic acidemia and anorectal anomalies in three siblings.
Topics: Amino Acid Metabolism, Inborn Errors; Anal Canal; Consanguinity; Female; Glycine; Humans; Infant; In | 1977 |
Isovalerylglycine detection by thin-layer chromatography: additional observations.
Topics: Child; Chromatography, Gas; Chromatography, Thin Layer; Evaluation Studies as Topic; Glycine; Humans | 1975 |
Hyperglycinemia and propionyl coA carboxylase deficiency and episodic severe illness without consistent ketosis.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Citrates; Coenzyme A; Creatinine; Croto | 1975 |
The vitamin B12-deficient rat as a possible model of ketotic hyperglycinemia.
Topics: Acidosis; Animals; Biotin; Carbon Dioxide; Carboxy-Lyases; Glycine; Glycine Hydroxymethyltransferase | 1975 |
Therapeutic effects of glycine in isovaleric acidemia.
Topics: Acidosis; Alkalies; Amino Acid Metabolism, Inborn Errors; Child; Female; Glycine; Humans; Inactivati | 1976 |
[Beta-ketothiolase deficiency: a case of ketoacidosis with hyperglycinemia].
Topics: Acetyl-CoA C-Acyltransferase; Female; Glycine; Humans; Infant; Ketosis; Metabolism, Inborn Errors | 1992 |
Dextromethorphan and high-dose benzoate therapy for nonketotic hyperglycinemia in an infant.
Topics: Benzoates; Benzoic Acid; Dextromethorphan; Electroencephalography; Glycine; Humans; Infant; Infant, | 1992 |
Nonketotic hyperglycinemia: studies in an atypical variant.
Topics: Adult; Developmental Disabilities; Glycine; Humans; Intellectual Disability; Ketosis; Male; Metaboli | 1989 |
Acetoacetyl CoA thiolase deficiency presenting as ketotic hypoglycemia.
Topics: Acetoacetates; Acetyl-CoA C-Acetyltransferase; Acetyltransferases; Acidosis; Female; Glycine; Humans | 1987 |
3-Ketothiolase deficiency.
Topics: 3-Hydroxybutyric Acid; Acetyl Coenzyme A; Acetyl-CoA C-Acyltransferase; Acyl Coenzyme A; Acyltransfe | 1986 |