proline and DiGeorge Syndrome

proline has been researched along with DiGeorge Syndrome in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (50.00)29.6817
2010's3 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Crabtree, GW; Gogos, JA1
Tse, DHY; van Amelsvoort, T; Vingerhoets, C1
de Sonneville, LM; Hidding, E; Swaab, H; van Engeland, H; Vorstman, JA1
Beemer, FA; de Sain, MG; Dorland, B; Emanuel, BS; Kahn, RS; Kemner, C; Rappaport, EF; Sijmens-Morcus, ME; Sprong, M; Turetsky, BI; van Engeland, H; Vorstman, JA1
Allio, G; Bou, J; Campion, D; Demilly, C; Drouin, V; Fouldrin, G; Frébourg, T; Haouzir, S; Hecketsweiler, B; Houy, E; Jacquet, H; Petit, M; Raux, G; Thibaut, F1
Afenjar, A; Alembik, Y; Bou, J; Brévière, GM; Bumsel, E; Campion, D; Carlier, M; Coizet, C; Demily, C; Di Rosa, G; Drouin-Garraud, V; Fantini, C; Frebourg, T; Gérard-Desplanches, A; Hannequin, D; Hecketsweiler, B; Heron, D; Lacombe, D; Layet, V; Legallic, S; Lemarchand, M; Manouvrier-Hanu, S; Nolen, MC; Opolczynski, G; Petit, M; Philip, N; Philippe, A; Pustorino, G; Raux, G; Sarda, P; Swillen, A; Thibaut, F; van Amelsvoort, T; Vogels, A; Zinkstok, J1

Other Studies

6 other study(ies) available for proline and DiGeorge Syndrome

ArticleYear
Role of Endogenous Metabolite Alterations in Neuropsychiatric Disease.
    ACS chemical neuroscience, 2018, 09-19, Volume: 9, Issue:9

    Topics: DiGeorge Syndrome; gamma-Aminobutyric Acid; Humans; Metabolism, Inborn Errors; Metabolomics; Molecular Mimicry; Neuronal Plasticity; Neurotransmitter Agents; Proline; Proline Oxidase; Schizophrenia; Schizophrenic Psychology

2018
Riluzole effectively treats psychotic symptoms and improves cognition in 22q11.2 deletion syndrome: A clinical case.
    European journal of medical genetics, 2019, Volume: 62, Issue:8

    Topics: Adult; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Female; Glutamic Acid; Humans; Proline; Proline Oxidase; Psychotic Disorders; Riluzole; Young Adult

2019
The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome.
    Clinical genetics, 2016, Volume: 90, Issue:5

    Topics: Adolescent; Autistic Disorder; Catechol O-Methyltransferase; Child; DiGeorge Syndrome; Dopamine; Epistasis, Genetic; Face; Female; Genotype; Humans; Male; Penetrance; Proline; Sequence Deletion; Social Behavior

2016
Proline affects brain function in 22q11DS children with the low activity COMT 158 allele.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2009, Volume: 34, Issue:3

    Topics: Adolescent; Alleles; Catechol O-Methyltransferase; Child; DiGeorge Syndrome; Dopamine; Electroencephalography; Female; Genotype; Humans; Male; Ocular Motility Disorders; Prefrontal Cortex; Proline; Proline Oxidase; Reflex, Startle; Sensory Gating

2009
PRODH mutations and hyperprolinemia in a subset of schizophrenic patients.
    Human molecular genetics, 2002, Sep-15, Volume: 11, Issue:19

    Topics: Amino Acid Substitution; DiGeorge Syndrome; Female; Humans; Male; Mutation, Missense; Pedigree; Proline; Proline Oxidase; Schizophrenia; Sequence Deletion

2002
Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
    Human molecular genetics, 2007, Jan-01, Volume: 16, Issue:1

    Topics: Adolescent; Adult; Alleles; Catechol O-Methyltransferase; Chromosome Deletion; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Epilepsy; Female; Genetic Predisposition to Disease; Humans; Intellectual Disability; Male; Methionine; Middle Aged; Phenotype; Proline; Proline Oxidase; Psychotic Disorders; Risk Factors

2007