glycine has been researched along with Developmental Psychomotor Disorders in 11 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Glycine encephalopathy, also known as nonketotic hyperglycinemia (NKH), is an autosomal recessive disorder caused by a defect in the glycine cleavage system." | 3.72 | Natural history of nonketotic hyperglycinemia in 65 patients. ( Applegarth, D; Hamosh, A; Hoover-Fong, JE; Shah, S; Toone, J; Van Hove, JL, 2004) |
| "Congenital microcephaly, intractable seizures and severe psychomotor retardation characterize 3-phosphoglycerate dehydrogenase (3-PGDH) deficiency, a disorder of L-serine biosynthesis." | 3.71 | Congenital microcephaly and seizures due to 3-phosphoglycerate dehydrogenase deficiency: outcome of treatment with amino acids. ( De Koning, TJ; Dorland, L; Duran, M; Gooskens, R; Jaeken, J; Pineda, M; Poll-The, BT; Van Maldergem, L, 2002) |
| "Serine concentrations were markedly decreased in the cerebrospinal fluid of two brothers with congenital microcephaly, profound psychomotor retardation, hypertonia, epilepsy, growth retardation, and hypogonadism." | 3.69 | 3-Phosphoglycerate dehydrogenase deficiency: an inborn error of serine biosynthesis. ( Carchon, H; Detheux, M; Foulon, M; Jaeken, J; Van Maldergem, L; Van Schaftingen, E, 1996) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (45.45) | 18.7374 |
| 1990's | 2 (18.18) | 18.2507 |
| 2000's | 3 (27.27) | 29.6817 |
| 2010's | 1 (9.09) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Glinton, KE | 1 |
| Benke, PJ | 1 |
| Lines, MA | 1 |
| Geraghty, MT | 1 |
| Chakraborty, P | 1 |
| Al-Dirbashi, OY | 1 |
| Jiang, Y | 1 |
| Kennedy, AD | 1 |
| Grotewiel, MS | 1 |
| Sutton, VR | 1 |
| Elsea, SH | 1 |
| El-Hattab, AW | 1 |
| De Koning, TJ | 1 |
| Duran, M | 1 |
| Van Maldergem, L | 2 |
| Pineda, M | 1 |
| Dorland, L | 1 |
| Gooskens, R | 1 |
| Jaeken, J | 2 |
| Poll-The, BT | 1 |
| Battini, R | 1 |
| Leuzzi, V | 1 |
| Carducci, C | 1 |
| Tosetti, M | 1 |
| Bianchi, MC | 1 |
| Item, CB | 1 |
| Stöckler-Ipsiroglu, S | 1 |
| Cioni, G | 1 |
| Hoover-Fong, JE | 1 |
| Shah, S | 1 |
| Van Hove, JL | 1 |
| Applegarth, D | 1 |
| Toone, J | 1 |
| Hamosh, A | 1 |
| MacDermot, KD | 1 |
| Nelson, W | 1 |
| Reichert, CM | 1 |
| Schulman, JD | 1 |
| Detheux, M | 1 |
| Foulon, M | 1 |
| Carchon, H | 1 |
| Van Schaftingen, E | 1 |
| Lu, FL | 1 |
| Wang, PJ | 1 |
| Hwu, WL | 1 |
| Tsou Yau, KI | 1 |
| Wang, TR | 1 |
| von Wendt, L | 1 |
| Similä, S | 2 |
| Hirvasniemi, A | 1 |
| Suvanto, E | 1 |
| Hayasaka, K | 1 |
| Tada, K | 1 |
| Fueki, N | 1 |
| Nakamura, Y | 1 |
| Nyhan, WL | 1 |
| Schmidt, K | 1 |
| Packman, S | 1 |
| Seashore, MR | 1 |
| Haan, E | 1 |
| Danks, DM | 1 |
| Visakorpi, JK | 1 |
| Larbre, F | 1 |
| Hartemann, E | 1 |
| Guibaud, P | 1 |
| Collombel, C | 1 |
| Guerrier, G | 1 |
11 other studies available for glycine and Developmental Psychomotor Disorders
| Article | Year |
|---|---|
Disturbed phospholipid metabolism in serine biosynthesis defects revealed by metabolomic profiling.
Topics: Carbohydrate Metabolism, Inborn Errors; Cell Differentiation; Child; Child, Preschool; Dietary Suppl | 2018 |
Congenital microcephaly and seizures due to 3-phosphoglycerate dehydrogenase deficiency: outcome of treatment with amino acids.
Topics: Carbohydrate Dehydrogenases; Child; Child, Preschool; Female; Glycine; Humans; Infant; Male; Microce | 2002 |
Creatine depletion in a new case with AGAT deficiency: clinical and genetic study in a large pedigree.
Topics: Amidinotransferases; Child, Preschool; Creatine; Female; Glycine; Guanidinoacetate N-Methyltransfera | 2002 |
Natural history of nonketotic hyperglycinemia in 65 patients.
Topics: Adolescent; Age of Onset; Agenesis of Corpus Callosum; Anticonvulsants; Apnea; Child; Child, Prescho | 2004 |
Attempts at use of strychnine sulfate in the treatment of nonketotic hyperglycinemia.
Topics: Amino Acid Metabolism, Inborn Errors; Brain; Glycine; Humans; Infant; Infant, Newborn; Intellectual | 1980 |
3-Phosphoglycerate dehydrogenase deficiency: an inborn error of serine biosynthesis.
Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Dehydrogenases; Fibroblasts; Glycine; Humans; Inf | 1996 |
Neonatal type of nonketotic hyperglycinemia.
Topics: Ammonia; Brain; Female; Glycine; Humans; Infant, Newborn; Lactic Acid; Magnetic Resonance Imaging; M | 1999 |
Nonketotic hyperglycinemia: a clinical analysis of 19 Finnish patients.
Topics: Amino Acid Metabolism, Inborn Errors; Female; Finland; Glycine; Humans; Infant; Infant, Newborn; Int | 1978 |
Nonketotic hyperglycinemia: analyses of glycine cleavage system in typical and atypical cases.
Topics: Amino Acid Oxidoreductases; Aminomethyltransferase; Brain; Carrier Proteins; Glycine; Humans; Hydrox | 1987 |
Clinical findings in three patients with nonketotic hyperglycinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Electroencephalography; Glycine; Humans; Infant; Infant, Newbo | 1970 |
[Glycinosis with acidocetosis of late revelation and favorable evolution].
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Glutamates; Gl | 1970 |