SELMI, RAED
SELMI, RAED
Universita' degli Studi di MILANO
Mostra
records
Risultati 1 - 6 di 6 (tempo di esecuzione: 0.004 secondi).
Alexander disease infantile form presenting with GFAP gene DNA mutation in exon 1 with substitution missense c.715C>T in p.R239C : a case report
2013 E. Salvatici, S. Barberi, F. Salvini, R. Selmi, V. Rovelli, E. Riva
Is phenylalanine (Phe) loading test still necessary for hyperphenylalaninemia patient with basal plasma level < 360 micromol/l?
2013 R. Selmi, E. Salvatici, V. Rovelli, S. Paci, E. Riva
Genotype, basal PHE levels and type of nourishment as predictive factors of the BH4 loading test response in phenylketonuria (PKU) affected patients
2013 E. Riva, C. Paramithiotti, E. Salvatici, R. Selmi, S. Vincenti, S. Paci, M. Giovannini
Could neurological symptomatology precede an acute metabolic crisis in patient affected by propionic aciduria (PA)? A particular case report
2012 S. Paci, S. Vincenti, R. Selmi, E. Salvatici, E. Riva
Literature review and Case report : Treatment of recurrent attacks of idiopathic high-flow priapism in 13-year-old boy with Diazepam and local ice pad. Case report and literature review
2012 R. Selmi, F. Salvini, M. Castiglioni, G.M. Colpi, E. Riva
A new diagnosis of infantile form of alexander disease with a novel DNA mutation of the glial fibrillary acid protein gene (GFAP)
2011 E. Salvatici, R. Selmi, F. Salvini, E. Riva