Authors:
Grosso, M
Rescigno, G
Zevino, C
Matarazzo, M
Poggi, V
Izzo, P
Citation: M. Grosso et al., A rare case of compound heterozygosity for delta(+)27 and Hb Neapolis (Dhonburi) associated to an atypical beta-thalassemia phenotype, HAEMATOLOG, 86(9), 2001, pp. 985-986
Authors:
de Leon, MP
Varesco, L
Benatti, P
Sassatelli, R
Izzo, P
Scarano, MI
Rossi, GB
Di Gregorio, C
Gismondi, V
Percesepe, A
de Rosa, M
Roncucci, L
Citation: Mp. De Leon et al., Phenotype-genotype correlations in an extended family with adenomatosis coli and an unusual APC gene mutation, DIS COL REC, 44(11), 2001, pp. 1597-1604
Authors:
De Rosa, M
Fasano, C
Panariello, L
Scarano, MI
Belli, G
Iannelli, A
Ciciliano, F
Izzo, P
Citation: M. De Rosa et al., Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene, ONCOGENE, 19(13), 2000, pp. 1719-1723
Authors:
Izzo, P
Spagnuolo, A
Manicone, A
Nazzaro, P
Lauta, VM
Citation: P. Izzo et al., Reduced deformability of erythrocytes as feature of congenital dyserythropoietic anaemia type II (HEMPAS), CL HEMORH M, 21(3-4), 1999, pp. 425-430
Authors:
De Rosa, M
Scarano, MI
Panariello, L
Carlomagno, N
Rossi, GB
Tempesta, A
Borgheresi, P
Renda, A
Izzo, P
Citation: M. De Rosa et al., Three submicroscopic deletions at the APC locus and their rapid detection by quantitative-PCR analysis, EUR J HUM G, 7(6), 1999, pp. 695-703
Authors:
Santamaria, R
Vitagliano, L
Tamasi, S
Izzo, P
Zancan, L
Zagari, A
Salvatore, F
Citation: R. Santamaria et al., Novel six-nucleotide deletion in the hepatic fructose-1,6-bisphosphate aldolase gene in a patient with hereditary fructose intolerance and enzyme structure-function implications, EUR J HUM G, 7(4), 1999, pp. 409-414
Authors:
Costanzo, P
Lupo, A
Medugno, L
D'Agostino, P
Zevino, C
Izzo, P
Citation: P. Costanzo et al., PKC-dependent phosphorylation of the p97 repressor regulates the transcription of aldolase A L-type promoter, FEBS LETTER, 454(1-2), 1999, pp. 61-66