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Elizabeth E Half

Showing results (11-20 of 21) with videos related to

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International Journal of Cancer|July 9, 2026
Colorectal Cancer Screening in Hereditary and Familial High-Risk Populations: Best Practices and Future DirectionsOphir Gilad, Francesc Balaguer, Elizabeth E Half, et al.
Journal of the American Medical Informatics Association : JAMIA|February 26, 2016
Development and validation of a predictive model for detection of colorectal cancer in primary care by analysis of complete blood counts: a binational retrospective studyYaron Kinar, Nir Kalkstein, Pinchas Akiva, et al.
United European Gastroenterology Journal|June 2, 2021
Post-polypectomy surveillance colonoscopy: Comparison of the updated guidelinesNaim Abu-Freha, Lior H Katz, Revital Kariv, et al.
Cancer|January 5, 2024
Colorectal cancer screening at age 45 years in Israel: Cost-effectiveness and global implicationsElizabeth E Half, Zohar Levi, Ajitha Mannalithara, et al.
Frontiers in Oncology|September 9, 2020
Intratumoral HLA-DR<sup>-</sup>/CD33<sup>+</sup>/CD11b<sup>+</sup> Myeloid-Derived Suppressor Cells Predict Response to Neoadjuvant Chemoradiotherapy in Locally Advanced Rectal CancerErez Hasnis, Aviva Dahan, Wissam Khoury, et al.
American Journal of Clinical Pathology|October 20, 2004
Frequent CpG island methylation in sporadic and syndromic gastric fundic gland polypsSusan C Abraham, Seun Ja Park, Marcia Cruz-Correa, et al.
Hereditary Cancer in Clinical Practice|January 21, 2022
Phenotypic diversity among juvenile polyposis syndrome patients from different ethnic backgroundLior Haim Katz, Rachel Gingold-Belfer, Elez Vainer, et al.
Journal of Medical Genetics|March 13, 2019
Homozygosity for CHEK2 p.Gly167Arg leads to a unique cancer syndrome with multiple complex chromosomal translocations in peripheral blood karyotypeTamar Paperna, Nitzan Sharon-Shwartzman, Alina Kurolap, et al.
Pediatric Blood & Cancer|November 7, 2015
Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and ConsanguinityHagit N Baris, Inbal Barnes-Kedar, Helen Toledano, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|February 5, 2023
High prevalence of MUTYH associated polyposis among minority populations in Israel, due to rare founder pathogenic variantsGili Reznick Levi, Yael Goldberg, Hanna Segev, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
International Journal of Cancer|July 9, 2026
Colorectal Cancer Screening in Hereditary and Familial High-Risk Populations: Best Practices and Future DirectionsOphir Gilad, Francesc Balaguer, Elizabeth E Half, et al.
Journal of the American Medical Informatics Association : JAMIA|February 26, 2016
Development and validation of a predictive model for detection of colorectal cancer in primary care by analysis of complete blood counts: a binational retrospective studyYaron Kinar, Nir Kalkstein, Pinchas Akiva, et al.
United European Gastroenterology Journal|June 2, 2021
Post-polypectomy surveillance colonoscopy: Comparison of the updated guidelinesNaim Abu-Freha, Lior H Katz, Revital Kariv, et al.
Cancer|January 5, 2024
Colorectal cancer screening at age 45 years in Israel: Cost-effectiveness and global implicationsElizabeth E Half, Zohar Levi, Ajitha Mannalithara, et al.
Frontiers in Oncology|September 9, 2020
Intratumoral HLA-DR<sup>-</sup>/CD33<sup>+</sup>/CD11b<sup>+</sup> Myeloid-Derived Suppressor Cells Predict Response to Neoadjuvant Chemoradiotherapy in Locally Advanced Rectal CancerErez Hasnis, Aviva Dahan, Wissam Khoury, et al.
American Journal of Clinical Pathology|October 20, 2004
Frequent CpG island methylation in sporadic and syndromic gastric fundic gland polypsSusan C Abraham, Seun Ja Park, Marcia Cruz-Correa, et al.
Hereditary Cancer in Clinical Practice|January 21, 2022
Phenotypic diversity among juvenile polyposis syndrome patients from different ethnic backgroundLior Haim Katz, Rachel Gingold-Belfer, Elez Vainer, et al.
Journal of Medical Genetics|March 13, 2019
Homozygosity for CHEK2 p.Gly167Arg leads to a unique cancer syndrome with multiple complex chromosomal translocations in peripheral blood karyotypeTamar Paperna, Nitzan Sharon-Shwartzman, Alina Kurolap, et al.
Pediatric Blood & Cancer|November 7, 2015
Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and ConsanguinityHagit N Baris, Inbal Barnes-Kedar, Helen Toledano, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|February 5, 2023
High prevalence of MUTYH associated polyposis among minority populations in Israel, due to rare founder pathogenic variantsGili Reznick Levi, Yael Goldberg, Hanna Segev, et al.
Pageof 3