glycine has been researched along with Auditory Processing Disorder, Central in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (27.27) | 29.6817 |
| 2010's | 7 (63.64) | 24.3611 |
| 2020's | 1 (9.09) | 2.80 |
| Authors | Studies |
|---|---|
| Balestrino, M | 1 |
| Adriano, E | 1 |
| Benoit, R | 1 |
| Samir, M | 1 |
| Boutin, J | 1 |
| Samuel, A | 1 |
| Brigitte, C | 1 |
| Dominique, D | 1 |
| Isabelle, RV | 1 |
| El-Gharbawy, AH | 1 |
| Goldstein, JL | 1 |
| Millington, DS | 1 |
| Vaisnins, AE | 1 |
| Schlune, A | 2 |
| Barshop, BA | 1 |
| Schulze, A | 3 |
| Koeberl, DD | 1 |
| Young, SP | 1 |
| Stockler-Ipsiroglu, S | 1 |
| van Karnebeek, C | 1 |
| Longo, N | 2 |
| Korenke, GC | 1 |
| Mercimek-Mahmutoglu, S | 1 |
| Marquart, I | 1 |
| Barshop, B | 1 |
| Grolik, C | 1 |
| Angle, B | 1 |
| Araújo, HC | 1 |
| Coskun, T | 1 |
| Diogo, L | 1 |
| Geraghty, M | 1 |
| Haliloglu, G | 1 |
| Konstantopoulou, V | 1 |
| Leuzzi, V | 1 |
| Levtova, A | 1 |
| Mackenzie, J | 1 |
| Maranda, B | 1 |
| Mhanni, AA | 1 |
| Mitchell, G | 1 |
| Morris, A | 1 |
| Newlove, T | 1 |
| Renaud, D | 1 |
| Scaglia, F | 1 |
| Valayannopoulos, V | 1 |
| van Spronsen, FJ | 1 |
| Verbruggen, KT | 1 |
| Yuskiv, N | 1 |
| Nyhan, W | 1 |
| Braissant, O | 2 |
| Pasquali, M | 1 |
| Schwarz, E | 1 |
| Jensen, M | 1 |
| Yuzyuk, T | 1 |
| DeBiase, I | 1 |
| Randall, H | 1 |
| Pitt, JJ | 1 |
| Tzanakos, N | 1 |
| Nguyen, T | 1 |
| Tran, C | 1 |
| Levandovskiy, V | 1 |
| Patel, V | 1 |
| Cortez, MA | 1 |
| Eminoglu, FT | 1 |
| Ozcelik, AA | 1 |
| Okur, I | 1 |
| Tumer, L | 1 |
| Biberoglu, G | 1 |
| Demir, E | 1 |
| Hasanoglu, A | 1 |
| Baumgartner, MR | 1 |
| Henry, H | 1 |
| Anselm, IA | 1 |
| Coulter, DL | 1 |
| Darras, BT | 1 |
1 review available for glycine and Auditory Processing Disorder, Central
| Article | Year |
|---|---|
AGAT, GAMT and SLC6A8 distribution in the central nervous system, in relation to creatine deficiency syndromes: a review.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Animals; Brain; Creatine; Developmental D | 2008 |
10 other studies available for glycine and Auditory Processing Disorder, Central
| Article | Year |
|---|---|
Presence of guanidinoacetate may compensate creatine absence and account for less statin-induced muscle damage in GAMT-deficient compared to AGAT-deficient mice.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Animals; Creatine; Developmental Disabili | 2020 |
LC-MS/MS measurements of urinary guanidinoacetic acid and creatine: Method optimization by deleting derivatization step.
Topics: Chromatography, High Pressure Liquid; Clinical Laboratory Techniques; Creatine; Glycine; Guanidinoac | 2019 |
Elevation of guanidinoacetate in newborn dried blood spots and impact of early treatment in GAMT deficiency.
Topics: Case-Control Studies; Child, Preschool; Creatine; Dried Blood Spot Testing; Early Diagnosis; Female; | 2013 |
Guanidinoacetate methyltransferase (GAMT) deficiency: outcomes in 48 individuals and recommendations for diagnosis, treatment and monitoring.
Topics: Adolescent; Adult; Arginine; Brain; Child; Child, Preschool; Combined Modality Therapy; Creatine; Fe | 2014 |
GAMT deficiency: 20 years of a treatable inborn error of metabolism.
Topics: Arginine; Creatine; Female; Glycine; Guanidinoacetate N-Methyltransferase; Humans; Intellectual Disa | 2014 |
Feasibility of newborn screening for guanidinoacetate methyltransferase (GAMT) deficiency.
Topics: Brain; Creatine; Dried Blood Spot Testing; False Positive Reactions; Feasibility Studies; Glycine; G | 2014 |
Newborn screening for guanidinoacetate methyl transferase deficiency.
Topics: Arginine; Creatine; Diet; Female; Glycine; Guanidinoacetate N-Methyltransferase; Humans; Intellectua | 2014 |
Systemic availability of guanidinoacetate affects GABAA receptor function and seizure threshold in GAMT deficient mice.
Topics: Animals; Electrocorticography; Glycine; Guanidinoacetate N-Methyltransferase; Language Development D | 2016 |
3-Methylcrotonyl-CoA carboxylase deficiency: phenotypic variability in a family.
Topics: Adult; Brain; Carbon-Carbon Ligases; Carnitine; Cells, Cultured; Child, Preschool; DNA Mutational An | 2009 |
Cardiac manifestations in a child with a novel mutation in creatine transporter gene SLC6A8.
Topics: Base Sequence; Brain Chemistry; Child; Child Behavior Disorders; Creatine; Developmental Disabilitie | 2008 |