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L Foretová

Showing results (11-20 of 28) with videos related to

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Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|May 15, 2010
[Our experience with analysis of the PTEN gene in patients suspected of having Cowden syndrome]P Vasovcák, L Foretová, A Puchmajerová, et al.
Casopis Lekaru Ceskych|February 24, 2001
A high occurrence of BRCA1 and BRCA2 mutations among Czech hereditary breast and breast-ovarian cancer familiesE Machácková, L Foretová, M Navrátilová, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|August 28, 2012
[Surgical prevention of breast carcinoma in patients with hereditary risk]L Dražan, J Veselý, P Hýža, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|December 23, 2015
[Recommended Extension of Indication Criteria for Genetic Testing of BRCA1 and BRCA2 Mutations in Hereditary Breast and Ovarian Cancer Syndrome]L Foretová, E Macháčková, M Palácová, et al.
European Journal of Gynaecological Oncology|May 8, 2008
Pathological complete response after primary chemotherapy in a mother and daughter with hereditary breast carcinoma: two case reportsB Melichar, P Fridrichová, S Lukesová, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|December 23, 2015
[Retrospective NGS Study in High-risk Hereditary Cancer Patients at Masaryk Memorial Cancer Institute]E Macháčková, J Hazova, E Sťahlová Hrabincová, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|August 28, 2012
[Diagnostics of breast cancer in high-risk women - our own experience]M Palácová, M Krásenská, A Ondračková, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|September 22, 2009
[Prerequisites for preimplantation genetic diagnosis (PGD in carriers of mutations responsible for hereditary cancers]R Hüttelová, Z Kleibl, J Rezátová, et al.
Neoplasma|September 8, 2007
PML protein expression in hereditary and sporadic breast cancerP Plevová, J Bouchal, M Fiurásková, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|December 23, 2015
[Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report]A Puchmajerová, K Švojgr, D Novotná, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|May 15, 2010
[Our experience with analysis of the PTEN gene in patients suspected of having Cowden syndrome]P Vasovcák, L Foretová, A Puchmajerová, et al.
Casopis Lekaru Ceskych|February 24, 2001
A high occurrence of BRCA1 and BRCA2 mutations among Czech hereditary breast and breast-ovarian cancer familiesE Machácková, L Foretová, M Navrátilová, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|August 28, 2012
[Surgical prevention of breast carcinoma in patients with hereditary risk]L Dražan, J Veselý, P Hýža, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|December 23, 2015
[Recommended Extension of Indication Criteria for Genetic Testing of BRCA1 and BRCA2 Mutations in Hereditary Breast and Ovarian Cancer Syndrome]L Foretová, E Macháčková, M Palácová, et al.
European Journal of Gynaecological Oncology|May 8, 2008
Pathological complete response after primary chemotherapy in a mother and daughter with hereditary breast carcinoma: two case reportsB Melichar, P Fridrichová, S Lukesová, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|December 23, 2015
[Retrospective NGS Study in High-risk Hereditary Cancer Patients at Masaryk Memorial Cancer Institute]E Macháčková, J Hazova, E Sťahlová Hrabincová, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|August 28, 2012
[Diagnostics of breast cancer in high-risk women - our own experience]M Palácová, M Krásenská, A Ondračková, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|September 22, 2009
[Prerequisites for preimplantation genetic diagnosis (PGD in carriers of mutations responsible for hereditary cancers]R Hüttelová, Z Kleibl, J Rezátová, et al.
Neoplasma|September 8, 2007
PML protein expression in hereditary and sporadic breast cancerP Plevová, J Bouchal, M Fiurásková, et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti|December 23, 2015
[Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report]A Puchmajerová, K Švojgr, D Novotná, et al.
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