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glycocyamine and Auditory Processing Disorder, Central

glycocyamine has been researched along with Auditory Processing Disorder, Central in 10 studies

glycocyamine: RN given refers to parent cpd; structure
guanidinoacetate : A monocarboxylic acid anion that is the conjugate base of guanidinoacetic acid, obtained by deprotonation of the carboxy group.
guanidinoacetic acid : The N-amidino derivative of glycine.

Research Excerpts

ExcerptRelevanceReference
" Here, we used Micro-Electrode Arrays (MEAs) to further investigate the electrophysiological effects of its acute and chronic administration in the networks of cultured neurons, either neocortical or hippocampal."1.72Lack of Epileptogenic Effects of the Creatine Precursor Guanidinoacetic Acid on Neuronal Cultures In Vitro. ( Adriano, E; Balestrino, M; Brofiga, M; Massobrio, P; Poggio, F; Tedesco, M, 2022)

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (20.00)29.6817
2010's6 (60.00)24.3611
2020's2 (20.00)2.80

Authors

AuthorsStudies
Poggio, F1
Brofiga, M1
Tedesco, M1
Massobrio, P1
Adriano, E2
Balestrino, M2
Benoit, R1
Samir, M1
Boutin, J1
Samuel, A1
Brigitte, C1
Dominique, D1
Isabelle, RV1
El-Gharbawy, AH1
Goldstein, JL1
Millington, DS1
Vaisnins, AE1
Schlune, A2
Barshop, BA1
Schulze, A3
Koeberl, DD1
Young, SP1
Stockler-Ipsiroglu, S1
van Karnebeek, C1
Longo, N2
Korenke, GC1
Mercimek-Mahmutoglu, S1
Marquart, I1
Barshop, B1
Grolik, C1
Angle, B1
Araújo, HC1
Coskun, T1
Diogo, L1
Geraghty, M1
Haliloglu, G1
Konstantopoulou, V1
Leuzzi, V1
Levtova, A1
Mackenzie, J1
Maranda, B1
Mhanni, AA1
Mitchell, G1
Morris, A1
Newlove, T1
Renaud, D1
Scaglia, F1
Valayannopoulos, V1
van Spronsen, FJ1
Verbruggen, KT1
Yuskiv, N1
Nyhan, W1
Braissant, O2
Pasquali, M1
Schwarz, E1
Jensen, M1
Yuzyuk, T1
DeBiase, I1
Randall, H1
Tran, C1
Levandovskiy, V1
Patel, V1
Cortez, MA1
Henry, H1
Anselm, IA1
Coulter, DL1
Darras, BT1

Reviews

1 review available for glycocyamine and Auditory Processing Disorder, Central

ArticleYear
AGAT, GAMT and SLC6A8 distribution in the central nervous system, in relation to creatine deficiency syndromes: a review.
    Journal of inherited metabolic disease, 2008, Volume: 31, Issue:2

    Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Animals; Brain; Creatine; Developmental D

2008

Other Studies

9 other studies available for glycocyamine and Auditory Processing Disorder, Central

ArticleYear
Lack of Epileptogenic Effects of the Creatine Precursor Guanidinoacetic Acid on Neuronal Cultures In Vitro.
    Biomolecules, 2022, 12-30, Volume: 13, Issue:1

    Topics: Brain; Creatine; Humans; Language Development Disorders; Neurons

2022
Presence of guanidinoacetate may compensate creatine absence and account for less statin-induced muscle damage in GAMT-deficient compared to AGAT-deficient mice.
    Amino acids, 2020, Volume: 52, Issue:4

    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.
    Clinica chimica acta; international journal of clinical chemistry, 2019, Volume: 493

    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.
    Molecular genetics and metabolism, 2013, Volume: 109, Issue:2

    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.
    Molecular genetics and metabolism, 2014, Volume: 111, Issue:1

    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.
    Molecular genetics and metabolism, 2014, Volume: 111, Issue:1

    Topics: Arginine; Creatine; Female; Glycine; Guanidinoacetate N-Methyltransferase; Humans; Intellectual Disa

2014
Feasibility of newborn screening for guanidinoacetate methyltransferase (GAMT) deficiency.
    Journal of inherited metabolic disease, 2014, Volume: 37, Issue:2

    Topics: Brain; Creatine; Dried Blood Spot Testing; False Positive Reactions; Feasibility Studies; Glycine; G

2014
Systemic availability of guanidinoacetate affects GABAA receptor function and seizure threshold in GAMT deficient mice.
    Amino acids, 2016, Volume: 48, Issue:8

    Topics: Animals; Electrocorticography; Glycine; Guanidinoacetate N-Methyltransferase; Language Development D

2016
Cardiac manifestations in a child with a novel mutation in creatine transporter gene SLC6A8.
    Neurology, 2008, Apr-29, Volume: 70, Issue:18

    Topics: Base Sequence; Brain Chemistry; Child; Child Behavior Disorders; Creatine; Developmental Disabilitie

2008