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Irene Konstantopoulou

Showing results (1-10 of 74) with videos related to

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Genomics|October 14, 2020
Pitfalls in variant annotation for hereditary cancer diagnostics: The example of Illumina® VariantStudio®Despoina Kalfakakou, Irene Konstantopoulou, Drakoulis Yannoukakos, et al.
Oncology (Williston Park, N.Y.)|July 18, 2024
Neoadjuvant Capecitabine Plus Temozolomide in Atypical Lung NETsGeorgios Evangelou, Ioannis Vamvakaris, Irene Konstantopoulou, et al.
Journal of B.U.ON. : Official Journal of the Balkan Union of Oncology|November 6, 2007
Hereditary cancer syndromesFlorentia Fostira, Georgia Thodi, Irene Konstantopoulou, et al.
Case Reports in Genetics|March 25, 2014
A Paternally Inherited BRCA1 Mutation Associated with an Unusual Aggressive Clinical PhenotypeFlorentia Fostira, Nikolaos Tsoukalas, Irene Konstantopoulou, et al.
Case Reports in Oncological Medicine|June 22, 2019
A Patient Affected with Serous Ovarian/Peritoneal Carcinoma Carrying the <i>FANCM</i> MutationAdamantia Nikolaidi, Irene Konstantopoulou, Nikolaos Pistalmantzian, et al.
European Journal of Cancer (Oxford, England : 1990)|December 19, 2006
Novel genomic rearrangements in the BRCA1 gene detected in Greek breast/ovarian cancer patientsSophia Armaou, Irene Konstantopoulou, Theodore Anagnostopoulos, et al.
Cancer Genetics|August 27, 2019
Prevalence and founder effect of the BRCA1 p.(Val1833Met) variant in the Greek population, with further evidence for pathogenicity and risk modificationMyrto Papamentzelopoulou, Paraskevi Apostolou, Florentia Fostira, et al.
Thoracic Cancer|May 11, 2022
Lung cancer as a predominant feature in a patient with Peutz-Jeghers syndrome: Case reportFlorentia Fostira, Elena Fountzilas, Kyriaki Papadopoulou, et al.
Cancer Genetics|April 4, 2015
CHEK2 c.1100delC allele is rarely identified in Greek breast cancer casesParaskevi Apostolou, Florentia Fostira, Myrto Papamentzelopoulou, et al.
Cancer Genetics|January 10, 2018
Genetic analysis and clinical description of Greek patients with Peutz-Jeghers syndrome: Creation of a National RegistryFlorentia Fostira, Vasiliki Mollaki, George Lypas, et al.
Pageof 8

Showing results (1-10 of 74) with videos related to

Sort By:
Pageof 8
Genomics|October 14, 2020
Pitfalls in variant annotation for hereditary cancer diagnostics: The example of Illumina® VariantStudio®Despoina Kalfakakou, Irene Konstantopoulou, Drakoulis Yannoukakos, et al.
Oncology (Williston Park, N.Y.)|July 18, 2024
Neoadjuvant Capecitabine Plus Temozolomide in Atypical Lung NETsGeorgios Evangelou, Ioannis Vamvakaris, Irene Konstantopoulou, et al.
Journal of B.U.ON. : Official Journal of the Balkan Union of Oncology|November 6, 2007
Hereditary cancer syndromesFlorentia Fostira, Georgia Thodi, Irene Konstantopoulou, et al.
Case Reports in Genetics|March 25, 2014
A Paternally Inherited BRCA1 Mutation Associated with an Unusual Aggressive Clinical PhenotypeFlorentia Fostira, Nikolaos Tsoukalas, Irene Konstantopoulou, et al.
Case Reports in Oncological Medicine|June 22, 2019
A Patient Affected with Serous Ovarian/Peritoneal Carcinoma Carrying the <i>FANCM</i> MutationAdamantia Nikolaidi, Irene Konstantopoulou, Nikolaos Pistalmantzian, et al.
European Journal of Cancer (Oxford, England : 1990)|December 19, 2006
Novel genomic rearrangements in the BRCA1 gene detected in Greek breast/ovarian cancer patientsSophia Armaou, Irene Konstantopoulou, Theodore Anagnostopoulos, et al.
Cancer Genetics|August 27, 2019
Prevalence and founder effect of the BRCA1 p.(Val1833Met) variant in the Greek population, with further evidence for pathogenicity and risk modificationMyrto Papamentzelopoulou, Paraskevi Apostolou, Florentia Fostira, et al.
Thoracic Cancer|May 11, 2022
Lung cancer as a predominant feature in a patient with Peutz-Jeghers syndrome: Case reportFlorentia Fostira, Elena Fountzilas, Kyriaki Papadopoulou, et al.
Cancer Genetics|April 4, 2015
CHEK2 c.1100delC allele is rarely identified in Greek breast cancer casesParaskevi Apostolou, Florentia Fostira, Myrto Papamentzelopoulou, et al.
Cancer Genetics|January 10, 2018
Genetic analysis and clinical description of Greek patients with Peutz-Jeghers syndrome: Creation of a National RegistryFlorentia Fostira, Vasiliki Mollaki, George Lypas, et al.
Pageof 8