about
Liver transplantation prevents progressive neurological impairment in argininemiaEverolimus enhances gemcitabine-induced cytotoxicity in bladder-cancer cell lines.The use of prealbumin concentration as a biomarker of nutritional status in treated phenylketonuric patients.Creatine and guanidinoacetate: diagnostic markers for inborn errors in creatine biosynthesis and transport.Age related reference values for urine creatine and guanidinoacetic acid concentration in children and adolescents by gas chromatography-mass spectrometry.Living with inborn errors of cholesterol biosynthesis: lessons from adult patients.Early-onset hyperargininaemia: a severe disorder?The ND1 T3308C mutation may be a mtDNA polymorphism. Report of two Portuguese patientsMacrocephaly as the presenting feature of L-2-hydroxyglutaric aciduria in a 5-month-old boyLethal dilated cardiomyopathy due to long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency3-Hydroxy-3-methylglutaric aciduria in Portuguese populationLiver transplantation in a case of argininaemiaGlycogen storage disease type IV presenting as hydrops fetalis
P50
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P50
description
researcher ORCID ID = 0000-0002-8139-216X
@en
wetenschapper
@nl
name
Maria Luís Cardoso
@ast
Maria Luís Cardoso
@en
Maria Luís Cardoso
@es
Maria Luís Cardoso
@nl
type
label
Maria Luís Cardoso
@ast
Maria Luís Cardoso
@en
Maria Luís Cardoso
@es
Maria Luís Cardoso
@nl
prefLabel
Maria Luís Cardoso
@ast
Maria Luís Cardoso
@en
Maria Luís Cardoso
@es
Maria Luís Cardoso
@nl
P106
P31
P496
0000-0002-8139-216X