Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene

Por IOLASCON, A., MELONI, A., COPPOLA, B., ROSATELLI, M. C.
Publicado em 2000

21-hydroxylase deficiency in Italy: a distinct distribution pattern of CYP21 mutations in a sample from southern Italy

Por BOBBA, A, MARRA, E, GIANNATTASIO, S, IOLASCON, A, MONNO, F, DI, M
Publicado em 1999

Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigels.

Por Iolascon, A, Parrella, T, Perrotta, S, Guardamagna, O, Coates, P M, Sartore, M, Surrey, S, Fortina, P
Publicado em 1994

Characterisation of CAH alleles with non-radioactive DNA single strand conformation polymorphism analysis of the CYP21 gene.

Por Bobba, A, Iolascon, A, Giannattasio, S, Albrizio, M, Sinisi, A, Prisco, F, Schettini, F, Marra, E
Publicado em 1997

Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search.

Por Gasparini, P, Miraglia del Giudice, E, Delaunay, J, Totaro, A, Granatiero, M, Melchionda, S, Zelante, L, Iolascon, A
Publicado em 1997

Reduced expression of transforming growth factor-beta receptor type III in high stage neuroblastomas

Por Iolascon, A, Giordani, L, Borriello, A, Carbone, R, Izzo, A, Tonini, G P, Gambini, C, Ragione, F Della
Publicado em 2000

CD55 is a HIF-2α marker with anti-adhesive and pro-invading properties in neuroblastoma

Por Cimmino, F, Avitabile, M, Pezone, L, Scalia, G, Montanaro, D, Andreozzi, M, Terracciano, L, Iolascon, A, Capasso, M
Publicado no Oncogenesis (2016)

Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter).

Por Carella, M, Stewart, G, Ajetunmobi, J F, Perrotta, S, Grootenboer, S, Tchernia, G, Delaunay, J, Totaro, A, Zelante, L, Gasparini, P, Iolascon, A
Publicado em 1998