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Page last updated: 2024-08-17

methionine and Pervasive Child Development Disorders

methionine has been researched along with Pervasive Child Development Disorders in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Abdelrahman, HM; Fattah, NR; Hashim, HM; Hassan, TH; Karam, RA; Mohammad, D; Rezk, NA1
Banerjee, R; Benga, I; Cornean, R; Craciun, EC; Dronca, E; Dronca, M; Endreffy, E; Ferencz, BK; Iftene, F; Kaucsár, T; Paşca, SP1
Altink, ME; Buitelaar, JK; Buschgens, CJ; Fliers, EA; Franke, B; Hartman, CA; Hoekstra, PJ; Minderaa, RB; Nijmeijer, JS; Ormel, J; Rommelse, NN; Sergeant, JA; Verhulst, FC1

Other Studies

3 other study(ies) available for methionine and Pervasive Child Development Disorders

ArticleYear
Catechol-O-methyltransferase Val158Met polymorphism and hyperactivity symptoms in Egyptian children with autism spectrum disorder.
    Research in developmental disabilities, 2013, Volume: 34, Issue:7

    Topics: Case-Control Studies; Catechol O-Methyltransferase; Child; Child Development Disorders, Pervasive; Egypt; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Humans; Methionine; Valine

2013
One carbon metabolism disturbances and the C677T MTHFR gene polymorphism in children with autism spectrum disorders.
    Journal of cellular and molecular medicine, 2009, Volume: 13, Issue:10

    Topics: Aminobutyrates; Carbon; Case-Control Studies; Child; Child Development Disorders, Pervasive; Female; Genetic Predisposition to Disease; Genotype; Glutathione; Homocysteine; Humans; Male; Metabolic Networks and Pathways; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Polymorphism, Single Nucleotide

2009
Perinatal risk factors interacting with catechol O-methyltransferase and the serotonin transporter gene predict ASD symptoms in children with ADHD.
    Journal of child psychology and psychiatry, and allied disciplines, 2010, Volume: 51, Issue:11

    Topics: Adolescent; Attention Deficit Disorder with Hyperactivity; Birth Weight; Catechol O-Methyltransferase; Child; Child Development Disorders, Pervasive; Female; Genetic Predisposition to Disease; Genotype; Humans; INDEL Mutation; Interpersonal Relations; Linear Models; Male; Maternal Behavior; Methionine; Netherlands; Polymorphism, Single Nucleotide; Pregnancy; Risk Factors; Sampling Studies; Serotonin Plasma Membrane Transport Proteins; Smoking; Stereotyped Behavior; Surveys and Questionnaires; Valine

2010