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International Journal of Cancer|March 20, 1998
MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancerM Genuardi, M Anti, E Capozzi, et al.
ESMO Open|May 21, 2022
Implementation of preventive and predictive BRCA testing in patients with breast, ovarian, pancreatic, and prostate cancer: a position paper of Italian Scientific SocietiesA Russo, L Incorvaia, E Capoluongo, et al.
Genes, Chromosomes & Cancer|January 1, 1997
Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancerA Viel, M Genuardi, E Capozzi, et al.
Clinical Genetics|April 27, 2011
Fabry disease: polymorphic haplotypes and a novel missense mutation in the GLA geneL Ferri, C Guido, G la Marca, et al.
Prenatal Diagnosis|August 12, 2004
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal surveyA Sensi, S Cavani, N Villa, et al.
Leukemia|February 23, 2016
A phase 2 study of three low-dose intensity subcutaneous bortezomib regimens in elderly frail patients with untreated multiple myelomaA Larocca, S Bringhen, M T Petrucci, et al.
ESMO Open|July 1, 2022
Predictors of germline status for hereditary melanoma: 5 years of multi-gene panel testing within the Italian Melanoma IntergroupW Bruno, B Dalmasso, M Barile, et al.
ESMO Gastrointestinal Oncology|February 6, 2026
ItaLynch: an ongoing Italian study to evaluate the feasibility of mainstreaming the diagnosis of Lynch syndrome in colorectal cancer patientsA Puccini, F Grillo, M Fassan, et al.
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