Silvia Santagata
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Explore the profile of Silvia Santagata including associated specialties, affiliations and a list of published articles.
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9
Citations
52
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Recent Articles
1.
Nardecchia F, Caciotti A, Giovanniello T, De Leo S, Ferri L, Galosi S, et al.
Int J Mol Sci
. 2022 Apr;
23(8).
PMID: 35457240
3-Methylglutaconic aciduria type I (MGCA1) is an inborn error of the leucine degradation pathway caused by pathogenic variants in the gene, which encodes 3-methylglutaconyl-coenzyme A hydratase (MGH). To date, MGCA1...
2.
di Carlo E, Santagata S, Sauro L, Tolve M, Manti F, Leuzzi V, et al.
J Chromatogr B Analyt Technol Biomed Life Sci
. 2021 Oct;
1185:122999.
PMID: 34715572
5-hydroxytryptophan (5HTP) and 3-O-methyldopa (3OMD) are CSF diagnostic biomarkers of the defect of aromatic L-amino acid decarboxylase (AADC), a rare inherited disorder of neurotransmitter synthesis which, if untreated, results in...
3.
Magro M, Baratella D, Colo V, Vallese F, Nicoletto C, Santagata S, et al.
Bioelectrochemistry
. 2019 Dec;
132:107418.
PMID: 31835109
A shell of nanostructured ferric tannates was spontaneously developed on the surface of naked maghemite nanoparticles (SAMNs, the core) by a simple wet reaction with tannic acid (TA). The as...
4.
Nardecchia F, Chiarotti F, Carducci C, Santagata S, Valentini G, Angeloni A, et al.
Eur J Pediatr
. 2017 May;
176(7):917-924.
PMID: 28540433
Conclusion: Common metabolic (blood Phe levels) and individual (age) factors implicated in the assessment of PKU outcome account only marginally and transiently for the variability of neopterin and biopterin excretion...
5.
Santagata S, di Carlo E, Carducci C, Leuzzi V, Angeloni A, Carducci C
Clin Chim Acta
. 2017 Jan;
466:145-151.
PMID: 28109742
Background: (6R)-5,6,7,8-tetrahydrobiopterin (BH4) deficiencies are rare inherited defects of synthesis or regeneration of BH4. Due to the resulting hyperphenylalaninemia (HPA), some of them are detected by newborn screening and require...
6.
Carducci C, Santagata S, Friedman J, Pasquini E, Carducci C, Tolve M, et al.
Mol Genet Metab
. 2015 Jul;
115(4):157-60.
PMID: 26123188
Sepiapterin reductase deficiency (SRD) causes depletion of biogenic amines in the brain, early onset motor disorder, and intellectual disability. The diagnostic marker for this rare disease is increased sepiapterin and...
7.
Magro M, Campos R, Baratella D, Ferreira M, Bonaiuto E, Corraducci V, et al.
J Agric Food Chem
. 2015 Jan;
63(3):912-20.
PMID: 25584520
Naked maghemite nanoparticles, namely, surface active maghemite nanoparticles (SAMNs), characterized by a diameter of about 10 nm, possessing peculiar colloidal stability, surface chemistry, and superparamagnetism, present fundamental requisites for the...
8.
Carducci C, Carducci C, Santagata S, Adriano E, Artiola C, Thellung S, et al.
BMC Neurosci
. 2012 Apr;
13:41.
PMID: 22536786
Background: The discovery of the inherited disorders of creatine (Cr) synthesis and transport in the last few years disclosed the importance of blood Cr supply for the normal functioning of...
9.
Carducci C, Santagata S, Leuzzi V, Carducci C, Artiola C, Giovanniello T, et al.
Clin Chim Acta
. 2005 Oct;
364(1-2):180-7.
PMID: 16197934
Background: Guanidinoacetate (GAA) and creatine (Cr) are reliable biochemical markers of primary creatine disorders. The aim of this study was to develop and validate a method for the determination of...