Francesca Nardecchia | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
Psychiatric disorders in adolescent and young adult patients with phenylketonuria	MOLECULAR GENETICS AND METABOLISM	2016
Erythrocyte-mediated delivery of recombinant enzymes	JOURNAL OF INHERITED METABOLIC DISEASE	2016
Vulnerability and resilience to phenylalanine in PKU patients.	JOURNAL OF INHERITED METABOLIC DISEASE	2016
Secondary pterins alteration in patients with phenylalanine hydroxylase deficit	JOURNAL OF INHERITED METABOLIC DISEASE	2016
Outcome in short chain acyl-CoA dehydrogenase deficiency (SCADD) detected by newborn screening (NBS)	JOURNAL OF INHERITED METABOLIC DISEASE	2016
Neurocognitive and neuroimaging outcome of early treated young adult PKU patients: A longitudinal study	MOLECULAR GENETICS AND METABOLISM	2015
The outcome of white matter abnormalities in early treated phenylketonuric patients. A retrospective longitudinal long-term study	MOLECULAR GENETICS AND METABOLISM	2015
Psychiatric disturbances in adolescent and adult phenylketonuric patients	JOURNAL OF INHERITED METABOLIC DISEASE	2015
Transient hyperphenylalaninemia due to heterozygous mutation in pyruvoyltetrahydropterin synthase (PTS) gene	JOURNAL OF INHERITED METABOLIC DISEASE	2015
Optic neuropathy in an adult PKU patient during long term follow-up	JOURNAL OF INHERITED METABOLIC DISEASE	2015