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Theofanis Zagoras

Showing results (1-10 of 9) with videos related to

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European Journal of Medical Genetics|December 21, 2014
Inherited 15q24 microdeletion syndrome in twins and their father with phenotypic variabilityLena Samuelsson, Theofanis Zagoras, Maria Hafström
Journal of the European Academy of Dermatology and Venereology : JEADV|September 24, 2022
Porokeratosis is one of the most common genodermatoses and is associated with an increased risk of keratinocyte cancer and melanomaRahime Inci, Theofanis Zagoras, Despoina Kantere, et al.
Acta Dermato-Venereologica|August 24, 2023
Incidence and Prevalence of 73 Different Genodermatoses: A Nationwide Study in SwedenTheofanis Zagoras, Rahime Inci, Despoina Kantere, et al.
International Journal of Oncology|May 3, 2014
A mutation in POLE predisposing to a multi-tumour phenotypeAnna Rohlin, Theofanis Zagoras, Staffan Nilsson, et al.
Gynecologic Oncology|July 16, 2015
The gynecological surveillance of women with Lynch syndrome in SwedenGerasimos Tzortzatos, Emil Andersson, Maria Soller, et al.
The Journal of Clinical Endocrinology and Metabolism|September 23, 2017
Corticotroph Pituitary Carcinoma in a Patient With Lynch Syndrome (LS) and Pituitary Tumors in a Nationwide LS CohortDaniel Bengtsson, Patrick Joost, Christos Aravidis, et al.
Genes, Chromosomes & Cancer|October 24, 2015
GREM1 and POLE variants in hereditary colorectal cancer syndromesAnna Rohlin, Frida Eiengård, Ulf Lundstam, et al.
Familial Cancer|October 4, 2016
Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testingAnna Rohlin, Eva Rambech, Anders Kvist, et al.
Genes, Chromosomes & Cancer|April 17, 2022
Merged testing for colorectal cancer syndromes and re-evaluation of genetic variants improve diagnostic yield: Results from a nationwide prospective cohortSara Svensson, Theofanis Zagoras, Christos Aravidis, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
European Journal of Medical Genetics|December 21, 2014
Inherited 15q24 microdeletion syndrome in twins and their father with phenotypic variabilityLena Samuelsson, Theofanis Zagoras, Maria Hafström
Journal of the European Academy of Dermatology and Venereology : JEADV|September 24, 2022
Porokeratosis is one of the most common genodermatoses and is associated with an increased risk of keratinocyte cancer and melanomaRahime Inci, Theofanis Zagoras, Despoina Kantere, et al.
Acta Dermato-Venereologica|August 24, 2023
Incidence and Prevalence of 73 Different Genodermatoses: A Nationwide Study in SwedenTheofanis Zagoras, Rahime Inci, Despoina Kantere, et al.
International Journal of Oncology|May 3, 2014
A mutation in POLE predisposing to a multi-tumour phenotypeAnna Rohlin, Theofanis Zagoras, Staffan Nilsson, et al.
Gynecologic Oncology|July 16, 2015
The gynecological surveillance of women with Lynch syndrome in SwedenGerasimos Tzortzatos, Emil Andersson, Maria Soller, et al.
The Journal of Clinical Endocrinology and Metabolism|September 23, 2017
Corticotroph Pituitary Carcinoma in a Patient With Lynch Syndrome (LS) and Pituitary Tumors in a Nationwide LS CohortDaniel Bengtsson, Patrick Joost, Christos Aravidis, et al.
Genes, Chromosomes & Cancer|October 24, 2015
GREM1 and POLE variants in hereditary colorectal cancer syndromesAnna Rohlin, Frida Eiengård, Ulf Lundstam, et al.
Familial Cancer|October 4, 2016
Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testingAnna Rohlin, Eva Rambech, Anders Kvist, et al.
Genes, Chromosomes & Cancer|April 17, 2022
Merged testing for colorectal cancer syndromes and re-evaluation of genetic variants improve diagnostic yield: Results from a nationwide prospective cohortSara Svensson, Theofanis Zagoras, Christos Aravidis, et al.
Pageof 1