Ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosum: variable expression of a single syndrome?

Por Silengo, M, Silvestro, L, Capizzi, G, Lerone, M, Seri, M, Rosaia, L, Romeo, G
Publicado em 1998

Molecular characterisation of a supernumerary ring chromosome in a patient with VATER association

Por CINTI, R., PRIOLO, M., LERONE, M., GIMELLI, G., SERI, M., SILENGO, M., RAVAZZOLO, R.
Publicado em 2001

Time-dependent current decline in cyclic GMP-gated bovine channels caused by point mutations in the pore region expressed in Xenopus oocytes.

Por Bucossi, G, Eismann, E, Sesti, F, Nizzari, M, Seri, M, Kaupp, U B, Torre, V
Publicado em 1996

Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervation

Por COSTA, M., FAVA, M., SERI, M., CUSANO, R., SANCANDI, M., FORABOSCO, P., LERONE, M., MARTUCCIELLO, G., ROMEO, G., CECCHERINI, I.
Publicado em 2000

Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome

Por Belloni, E., Martucciello, G., Verderio, D., Ponti, E., Seri, M., Jasonni, V., Torre, M., Ferrari, M., Tsui, L.-C., Scherer, S. W.
Publicado em 2000

Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic Phenotype

Por Wischmeijer, A., Magini, P., Giorda, R., Gnoli, M., Ciccone, R., Cecconi, I., Franzoni, E., Mazzanti, L., Romeo, G., Zuffardi, O., Seri, M.
Publicado em 2011

MYO7A mutation screening in Usher syndrome type I patients from diverse origins

Por Jaijo, T, Aller, E, Beneyto, M, Najera, C, Graziano, C, Turchetti, D, Seri, M, Ayuso, C, Baiget, M, Moreno, F, Morera, C, Perez‐Garrigues, H, Millan, J M
Publicado em 2007

Weekly oxaliplatin, 5-fluorouracil and folinic acid (OXALF) as first-line chemotherapy for elderly patients with advanced gastric cancer: results of a phase II trial

Por Vincenzi B, Spalletta B, La Cesa A, Giordani P, Baldelli AM, Testa E, Di Seri M, Catalano V, Graziano F, Santini D, Russo A, Caraglia M, Virzi V, Cascinu S, Tonini G
Publicado em 2006-05-01

Weekly oxaliplatin, 5-fluorouracil and folinic acid (OXALF) as first-line chemotherapy for elderly patients with advanced gastric cancer: results of a phase II trial

Por Santini, D, Graziano, F, Catalano, V, Di Seri, M, Testa, E, Baldelli, AM, Giordani, P, La Cesa, A, Spalletta, B, Vincenzi, B, Russo, A, Caraglia, M, Virzi, V, Cascinu, S, Tonini, G
Publicado em 2006

Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy.

Por Seri, M, Cusano, R, Forabosco, P, Cinti, R, Caroli, F, Picco, P, Bini, R, Morra, V B, De Michele, G, Lerone, M, Silengo, M, Pela, I, Borrone, C, Romeo, G, Devoto, M
Publicado em 1999

Preservation of clonal heterogeneity of the Pneumocystis carinii-specific CD4 T cell repertoire in HIV infected, asymptomatic individuals

Por LI PIRA, G, FENOGLIO, D, BOTTONE, L, TERRANOVA, P, PONTALI, E, CAROLI, F, SERI, M, CAILLIEZ, J-C, KOOPMAN, G, ACCOLLA, R, DEL GALDO, F, ABBATE, G, DE PALMA, R, MANCA, F
Publicado em 2002