Pediatría
Departamento
Maastricht University
Maastricht, HolandaPublicaciones en colaboración con investigadoras/es de Maastricht University (4)
2021
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Cystathionine ß-synthase deficiency in the E-HOD registry-part I: pyridoxine responsiveness as a determinant of biochemical and clinical phenotype at diagnosis
Journal of Inherited Metabolic Disease, Vol. 44, Núm. 3, pp. 677-692
2018
2008
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Evidence that the COMTVal158Met polymorphism moderates subclinical psychotic and affective symptoms in unaffected first-degree relatives of patients with schizophrenia
European Psychiatry, Vol. 23, Núm. 3, pp. 219-222
2006
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Associations between COMTVal158Met polymorphism and cognition: direct or indirect effects?
European Psychiatry, Vol. 21, Núm. 5, pp. 338-342