Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Genuardi

Showing results (91-100 of 101) with videos related to

Pageof 11
Sort By:
Annals of the New York Academy of Sciences|November 15, 2006
SDH mutations in patients affected by paraganglioma syndromes: a personal experienceM Mannelli, L Simi, T Ercolino, et al.
Community Genetics|June 5, 2004
Hereditary nonpolyposis colorectal cancer: an approach to the selection of candidates to genetic testing based on clinical and molecular characteristicsA Viel, M Genuardi, E Lucci-Cordisco, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 2, 2001
Molecular screening for hereditary nonpolyposis colorectal cancer: a prospective, population-based studyA Percesepe, F Borghi, M Menigatti, et al.
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.
Pageof 11

Showing results (91-100 of 101) with videos related to

Sort By:
Pageof 11
Annals of the New York Academy of Sciences|November 15, 2006
SDH mutations in patients affected by paraganglioma syndromes: a personal experienceM Mannelli, L Simi, T Ercolino, et al.
Community Genetics|June 5, 2004
Hereditary nonpolyposis colorectal cancer: an approach to the selection of candidates to genetic testing based on clinical and molecular characteristicsA Viel, M Genuardi, E Lucci-Cordisco, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 2, 2001
Molecular screening for hereditary nonpolyposis colorectal cancer: a prospective, population-based studyA Percesepe, F Borghi, M Menigatti, et al.
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.
Pageof 11