glycine has been researched along with Absence of Corpus Callosum in 6 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Nonketotic hyperglycinemia (NKH) or glycine encephalopathy is an autosomal recessive disorder of glycine metabolism resulting in an excessive accumulation of glycine in all body tissues, including the central nervous system." | 3.91 | Nonketotic Hyperglycinemia: Two Case Reports and Review. ( Al Futaisi, A; Al Murshidi, F; Al Thihli, K; Poothrikovil, RP, 2019) |
| "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) |
| "Classic nonketotic hyperglycinemia is caused by mutations or genomic changes in genes that encode the protein components of the glycine cleavage enzyme system." | 1.62 | Genotypic and phenotypic features in Turkish patients with classic nonketotic hyperglycinemia. ( Bayrak, H; Ceylaner, S; Kasapkara, ÇS; Kılıç, M; Küçükcongar, A; Olgaç, A; Yıldız, Y; Yüksel, D; Zenciroğlu, A, 2021) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 1 (16.67) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Poothrikovil, RP | 1 |
| Al Thihli, K | 1 |
| Al Futaisi, A | 1 |
| Al Murshidi, F | 1 |
| Bayrak, H | 1 |
| Yıldız, Y | 1 |
| Olgaç, A | 1 |
| Kasapkara, ÇS | 1 |
| Küçükcongar, A | 1 |
| Zenciroğlu, A | 1 |
| Yüksel, D | 1 |
| Ceylaner, S | 1 |
| Kılıç, M | 1 |
| Paupe, A | 1 |
| Bidat, L | 1 |
| Sonigo, P | 1 |
| Lenclen, R | 1 |
| Molho, M | 1 |
| Ville, Y | 1 |
| Hoover-Fong, JE | 1 |
| Shah, S | 1 |
| Van Hove, JL | 1 |
| Applegarth, D | 1 |
| Toone, J | 1 |
| Hamosh, A | 1 |
| Wariyar, UK | 1 |
| Welch, RJ | 1 |
| Milligan, DW | 1 |
| Perry, RH | 1 |
| Dobyns, WB | 1 |
6 other studies available for glycine and Absence of Corpus Callosum
| Article | Year |
|---|---|
Nonketotic Hyperglycinemia: Two Case Reports and Review.
Topics: Agenesis of Corpus Callosum; Apnea; Brain; Brain Diseases; Electroencephalography; Fatal Outcome; Fe | 2019 |
Genotypic and phenotypic features in Turkish patients with classic nonketotic hyperglycinemia.
Topics: Agenesis of Corpus Callosum; Amino Acid Oxidoreductases; Female; Genotype; Glycine; Humans; Hypergly | 2021 |
Prenatal diagnosis of hypoplasia of the corpus callosum in association with non-ketotic hyperglycinemia.
Topics: Abnormalities, Multiple; Agenesis of Corpus Callosum; Amino Acid Metabolism, Inborn Errors; Electroe | 2002 |
Natural history of nonketotic hyperglycinemia in 65 patients.
Topics: Adolescent; Age of Onset; Agenesis of Corpus Callosum; Anticonvulsants; Apnea; Child; Child, Prescho | 2004 |
Sonographic and pathological features of callosal hypoplasia in non-ketotic hyperglycinaemia.
Topics: Agenesis of Corpus Callosum; Amino Acid Metabolism, Inborn Errors; Corpus Callosum; Glycine; Humans; | 1990 |
Agenesis of the corpus callosum and gyral malformations are frequent manifestations of nonketotic hyperglycinemia.
Topics: Agenesis of Corpus Callosum; Amino Acid Metabolism, Inborn Errors; Brain; Cerebral Ventriculography; | 1989 |