glycine has been researched along with Diseases in Twins in 11 studies
Diseases in Twins: Disorders affecting TWINS, one or both, at any age.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The tendency towards metabolic acidosis developing during simple infections lead to the detection of hyperglycinemia which was shown to be caused by the rare inborn error of metabolism, which was shown to be a methylmalonic acidemia, in identical twins." | 3.66 | [Vitamin-B12-dependent methylmalonic acidemia in twins]. ( Hansen, HG; Heuer, R; Karsten, J; Kneer, J; Wulff, UC, 1983) |
| "Investigation of a 15-year old boy with progressive optic atrophy and spinocerebellar degeneration revealed elevated plasma, cerebrospinal fluid, and urine glycine concentrations." | 3.66 | Late-onset nonketotic hyperglycinemia and spinocerebellar degeneration. ( Berman, PH; Blazer-Yost, B; Segal, S; Steiman, GS; Yudkoff, M, 1979) |
| "Neonatal-type nonketotic hyperglycinemia treatment remains unsatisfactory, even if started early." | 1.32 | Poor outcome for neonatal-type nonketotic hyperglycinemia treated with high-dose sodium benzoate and dextromethorphan. ( Chien, YH; Chou, SP; Hsu, CC; Huang, A; Hwu, WL; Lee, WT; Lu, FL, 2004) |
| "In a newborn twin with haemolytic anaemia an unstable fetal haemoglobin was found to be the cause." | 1.25 | A new cause of haemolytic anaemia in the newborn. A description of an unstable fetal haemoglobin: F Poole, alpha2-G-gamma2 130 trptophan yeilds glycine. ( Deacon-Smith, RA; Kamuzora, H; Lee-Potter, JP; Lehmann, H; Simpkiss, MJ, 1975) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (63.64) | 18.7374 |
| 1990's | 2 (18.18) | 18.2507 |
| 2000's | 2 (18.18) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| KOPELMAN, H | 1 |
| ASATOOR, AM | 1 |
| MILNE, MD | 1 |
| Chien, YH | 1 |
| Hsu, CC | 1 |
| Huang, A | 1 |
| Chou, SP | 1 |
| Lu, FL | 1 |
| Lee, WT | 1 |
| Hwu, WL | 1 |
| Munhoz, RP | 1 |
| Wakutani, Y | 1 |
| Marras, C | 1 |
| Teive, HA | 1 |
| Raskin, S | 1 |
| Werneck, LC | 1 |
| Moreno, D | 1 |
| Sato, C | 1 |
| Lang, AE | 1 |
| Rogaeva, E | 1 |
| Pueschel, SM | 1 |
| Cha, CJ | 1 |
| Langon, T | 1 |
| Warburton, D | 1 |
| Boyle, RJ | 1 |
| Keats, JP | 1 |
| Vohr, B | 1 |
| Peuschel, S | 1 |
| Oh, W | 1 |
| Karsten, J | 1 |
| Hansen, HG | 1 |
| Heuer, R | 1 |
| Wulff, UC | 1 |
| Kneer, J | 1 |
| Kure, S | 1 |
| Shinka, T | 1 |
| Sakata, Y | 1 |
| Osamu, N | 1 |
| Takayanagi, M | 1 |
| Tada, K | 1 |
| Matsubara, Y | 1 |
| Narisawa, K | 1 |
| Cserhalmi-Friedman, PB | 1 |
| Grossman, J | 1 |
| Karpati, S | 1 |
| Ahmad, W | 1 |
| Horvath, A | 1 |
| Christiano, AM | 1 |
| Steiman, GS | 1 |
| Yudkoff, M | 1 |
| Berman, PH | 1 |
| Blazer-Yost, B | 1 |
| Segal, S | 1 |
| Steinmann, B | 1 |
| Gitzelmann, R | 1 |
| Lee-Potter, JP | 1 |
| Deacon-Smith, RA | 1 |
| Simpkiss, MJ | 1 |
| Kamuzora, H | 1 |
| Lehmann, H | 1 |
11 other studies available for glycine and Diseases in Twins
| Article | Year |
|---|---|
HYPERPROLINAEMIA AND HEREDITARY NEPHRITIS.
Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Blood; Blood Chemical | 1964 |
Poor outcome for neonatal-type nonketotic hyperglycinemia treated with high-dose sodium benzoate and dextromethorphan.
Topics: Brain; Child, Preschool; Chromosome Aberrations; Dextromethorphan; Diazepam; Disease Progression; Di | 2004 |
The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twins.
Topics: Adult; Age of Onset; Aged; Aged, 80 and over; Brazil; Diseases in Twins; Female; Glycine; Humans; Le | 2008 |
Therapeutic attempts in infants with nonketotic hyperglycinaemia.
Topics: Adrenocorticotropic Hormone; Amino Acid Metabolism, Inborn Errors; Benzoates; Benzoic Acid; Clonazep | 1981 |
Nonketotic hyperglycinemia. Effects of therapy with strychnine.
Topics: Amino Acid Metabolism, Inborn Errors; Clonazepam; Diseases in Twins; Epilepsies, Myoclonic; Female; | 1980 |
[Vitamin-B12-dependent methylmalonic acidemia in twins].
Topics: Acidosis; Diseases in Twins; Glycine; Humans; Infant; Malonates; Metabolism, Inborn Errors; Methylma | 1983 |
A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemia.
Topics: Amino Acid Metabolism, Inborn Errors; Aminomethyltransferase; Animals; Asian People; Aspartic Acid; | 1998 |
Identification of a de novo glycine substitution in the type VII collagen gene in a proband with mild dystrophic epidermolysis bullosa.
Topics: Base Sequence; Collagen; Diseases in Twins; DNA; Epidermolysis Bullosa Dystrophica; Female; Glycine; | 1999 |
Late-onset nonketotic hyperglycinemia and spinocerebellar degeneration.
Topics: Adolescent; Diseases in Twins; Glycine; Humans; Male; Nervous System Diseases; Optic Atrophy; Serine | 1979 |
Strychnine treatment attempted in newborn twins with severe nonketotic hyperglycinemia.
Topics: Diseases in Twins; Electroencephalography; Female; Glycine; Humans; Infant, Newborn; Infant, Newborn | 1979 |
A new cause of haemolytic anaemia in the newborn. A description of an unstable fetal haemoglobin: F Poole, alpha2-G-gamma2 130 trptophan yeilds glycine.
Topics: Amino Acid Sequence; Anemia, Hemolytic; Diseases in Twins; Fetal Hemoglobin; Glycine; Hemoglobins, A | 1975 |