| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S40142-012-0004-0 |
| P2888 | exact match | https://scigraph.springernature.com/pub.10.1007/s40142-012-0004-0 |
| P932 | PMC publication ID | 3603703 |
| P698 | PubMed publication ID | 23525354 |
| P5875 | ResearchGate publication ID | 236077254 |
| P50 | author | Jerry Vockley | Q42112236 |
| P2093 | author name string | Lisa Pan | |
| P2860 | cites work | Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia | Q28274064 |
| Monogenic traits are not simple: lessons from phenylketonuria | Q33677027 | ||
| Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathways | Q33918965 | ||
| Psychiatric manifestations revealing inborn errors of metabolism in adolescents and adults | Q34005690 | ||
| Tetrahydrobiopterin deficiencies without hyperphenylalaninemia: diagnosis and genetics of dopa-responsive dystonia and sepiapterin reductase deficiency. | Q34396185 | ||
| Repression of the human dihydrofolate reductase gene by a non-coding interfering transcript | Q34604327 | ||
| Psychiatric findings in Wolfram syndrome homozygotes | Q34611923 | ||
| Cognitive and adaptive functioning after liver transplantation for maple syrup urine disease: a case series. | Q34632629 | ||
| Psychiatric manifestations of homocystinuria due to cystathionine beta-synthase deficiency: prevalence, natural history, and relationship to neurologic impairment and vitamin B6-responsiveness | Q34691048 | ||
| Homocysteine, folate, methylation, and monoamine metabolism in depression | Q35458595 | ||
| Metabolism as a complex genetic trait, a systems biology approach: implications for inborn errors of metabolism and clinical diseases | Q37287373 | ||
| Metabolomics tools for identifying biomarkers for neuropsychiatric diseases | Q37419784 | ||
| The neuropharmacology of implicit learning | Q37883050 | ||
| Tetrahydrobiopterin: biochemistry and pathophysiology | Q37922206 | ||
| Adult phenylketonuria outcome and management | Q37938198 | ||
| Impaired mitochondrial function in psychiatric disorders | Q38003304 | ||
| Erratum: GTP-cyclohydrolase deficiency responsive to sapropterin and 5-HTP supplementation: relief of treatment-refractory depression and suicidal behaviour | Q39255679 | ||
| GTP-cyclohydrolase deficiency responsive to sapropterin and 5-HTP supplementation: relief of treatment-refractory depression and suicidal behaviour | Q39274193 | ||
| Guanosine triphosphate cyclohydrolase I deficiency: early diagnosis by routine urine pteridine screening. | Q42224002 | ||
| Neurochemical modulation of response inhibition and probabilistic learning in humans | Q42794222 | ||
| An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people | Q43136367 | ||
| Screening for cognitive and social-emotional problems in individuals with PKU: tools for use in the metabolic clinic | Q43177842 | ||
| Psychomotor retardation, spastic paraplegia, cerebellar ataxia and dyskinesia associated with low 5-methyltetrahydrofolate in cerebrospinal fluid: a novel neurometabolic condition responding to folinic acid substitution | Q44305300 | ||
| Acute postpartum mental status change and coma caused by previously undiagnosed ornithine transcarbamylase deficiency | Q44648397 | ||
| Depression symptoms, low-grade inflammatory activity, and new targets for clinical intervention. | Q48839657 | ||
| Cerebral folate deficiency: a neurometabolic syndrome? | Q50795070 | ||
| Anxiety and depression in the acute porphyrias. | Q50948081 | ||
| Neurocognitive profile in a case of maple syrup urine disease. | Q51579447 | ||
| Neuropsychiatric aspects of treated Wilson's disease. | Q51867020 | ||
| A preliminary metabolomic analysis of older adults with and without depression. | Q53586508 | ||
| Cerebral folate deficiency | Q60508373 | ||
| Cerebral folate deficiency | Q67224945 | ||
| Folate deficiency, biopterin and monoamine metabolism in depression | Q67467359 | ||
| Differential diagnosis of tetrahydrobiopterin deficiency | Q69965649 | ||
| Misdiagnosed postpartum psychosis revealing a late-onset urea cycle disorder | Q84277614 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 65-70 | |
| P577 | publication date | 2013-01-08 | |
| P1433 | published in | Current genetic medicine reports | Q27724648 |
| P1476 | title | Neuropsychiatric Symptoms in Inborn Errors of Metabolism: Incorporation of Genomic and Metabolomic Analysis into Therapeutics and Prevention | |
| P478 | volume | 1 |
| Q88220686 | Prophylactic ketamine alters nucleotide and neurotransmitter metabolism in brain and plasma following stress | cites work | P2860 |
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