asparagine and Autistic Disorder

asparagine has been researched along with Autistic Disorder in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aldred, S; Fitzgerald, M; Moore, KM; Waring, RH1
Anckarsäter, H; Betancur, C; Buxbaum, JD; Cai, G; Chaste, P; Gillberg, C; Goldsmith, J; Hollander, E; Leboyer, M; Nygren, G; Rastam, M; Reichert, J; Silverman, JM; Smith, CJ; Verloes, A1
Bottini, N; Curatolo, P; De Luca, D; Elia, M; Fiumara, A; Lucarelli, P; Porfirio, MC; Saccucci, P1

Other Studies

3 other study(ies) available for asparagine and Autistic Disorder

ArticleYear
Plasma amino acid levels in children with autism and their families.
    Journal of autism and developmental disorders, 2003, Volume: 33, Issue:1

    Topics: Adolescent; Alanine; Amino Acids; Asparagine; Asperger Syndrome; Autistic Disorder; Brain Diseases, Metabolic, Inborn; Child; Child, Preschool; Family; Female; Glutamic Acid; Glutamine; Humans; Lysine; Male; Phenylalanine; Tyrosine

2003
Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly.
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2007, Jun-05, Volume: 144B, Issue:4

    Topics: Abnormalities, Multiple; Adolescent; Adult; Amino Acid Sequence; Asparagine; Aspartic Acid; Autistic Disorder; Child; Child, Preschool; Craniofacial Abnormalities; DNA Mutational Analysis; Exons; Female; Genetic Testing; Humans; Introns; Male; Molecular Sequence Data; Mutation; PTEN Phosphohydrolase; Syndrome

2007
Autism: evidence of association with adenosine deaminase genetic polymorphism.
    Neurogenetics, 2001, Volume: 3, Issue:2

    Topics: Adenosine Deaminase; Adolescent; Alleles; Amino Acid Substitution; Asparagine; Aspartic Acid; Autistic Disorder; Child; Child, Preschool; Female; Genotype; Humans; Italy; Male; Polymorphism, Genetic; Reference Values; Risk Factors; White People

2001