proline has been researched along with DiGeorge Syndrome in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (50.00) | 29.6817 |
2010's | 3 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Crabtree, GW; Gogos, JA | 1 |
Tse, DHY; van Amelsvoort, T; Vingerhoets, C | 1 |
de Sonneville, LM; Hidding, E; Swaab, H; van Engeland, H; Vorstman, JA | 1 |
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, JA | 1 |
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, F | 1 |
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, J | 1 |
6 other study(ies) available for proline and DiGeorge Syndrome
Article | Year |
---|---|
Role of Endogenous Metabolite Alterations in Neuropsychiatric Disease.
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.
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.
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.
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.
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.
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 |