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British Journal of Cancer
|
December 17, 2015
PARP inhibitors in ovarian cancer
David Cibula, Judith Balmaña
Medicina Clinica
|
May 16, 2009
[Predictive models for identification of germline mutation carriers in Lynch syndrome]
Isela Quispe, Judith Balmaña
Journal of the National Cancer Institute
|
August 29, 2015
BRIP1 as an ovarian cancer susceptibility gene: ready for the clinic?
Judith Balmaña, Susan M Domchek
Cancer
|
April 22, 2006
BRAF mutations in colorectal carcinoma suggest two entities of microsatellite-unstable tumors
Eduardo Vilar, Judith Balmaña, Eloy Espín
Familial Cancer
|
April 5, 2013
Prediction models in Lynch syndrome
Fay Kastrinos, Judith Balmaña, Sapna Syngal
Familial Cancer
|
November 27, 2009
Heterogeneous prevalence of recurrent BRCA1 and BRCA2 mutations in Spain according to the geographical area: implications for genetic testing
Orland Diez, Sara Gutiérrez-Enríquez, Judith Balmaña
ESMO Open
|
June 25, 2019
Controversies in oncology: are genomic tests quantifying homologous recombination repair deficiency (HRD) useful for treatment decision making?
Benedetta Pellegrino, Joaquin Mateo, Violeta Serra, et al.
Tumori
|
July 30, 2015
Screening for Lynch syndrome among patients with newly diagnosed endometrial cancer: a comprehensive review
Elena Aguirre, Begoña Graña, Miguel Boudet, et al.
The American Journal of Gastroenterology
|
March 16, 2007
Attitudes toward prenatal genetic testing in patients with familial adenomatous polyposis
Fay Kastrinos, Elena M Stoffel, Judith Balmaña, et al.
Breast Cancer Research and Treatment
|
April 27, 2007
Detection of the CHEK2 1100delC mutation by MLPA BRCA1/2 analysis: a worthwhile strategy for its clinical applicability in 1100delC low-frequency populations?
Sara Gutiérrez-Enríquez, Judith Balmaña, Montserrat Baiget, et al.
Page
of 20
Search research articles
Search
Showing results (1-10 of 193) with videos related to
Sort By:
Page
of 20
British Journal of Cancer
|
December 17, 2015
PARP inhibitors in ovarian cancer
David Cibula, Judith Balmaña
Medicina Clinica
|
May 16, 2009
[Predictive models for identification of germline mutation carriers in Lynch syndrome]
Isela Quispe, Judith Balmaña
Journal of the National Cancer Institute
|
August 29, 2015
BRIP1 as an ovarian cancer susceptibility gene: ready for the clinic?
Judith Balmaña, Susan M Domchek
Cancer
|
April 22, 2006
BRAF mutations in colorectal carcinoma suggest two entities of microsatellite-unstable tumors
Eduardo Vilar, Judith Balmaña, Eloy Espín
Familial Cancer
|
April 5, 2013
Prediction models in Lynch syndrome
Fay Kastrinos, Judith Balmaña, Sapna Syngal
Familial Cancer
|
November 27, 2009
Heterogeneous prevalence of recurrent BRCA1 and BRCA2 mutations in Spain according to the geographical area: implications for genetic testing
Orland Diez, Sara Gutiérrez-Enríquez, Judith Balmaña
ESMO Open
|
June 25, 2019
Controversies in oncology: are genomic tests quantifying homologous recombination repair deficiency (HRD) useful for treatment decision making?
Benedetta Pellegrino, Joaquin Mateo, Violeta Serra, et al.
Tumori
|
July 30, 2015
Screening for Lynch syndrome among patients with newly diagnosed endometrial cancer: a comprehensive review
Elena Aguirre, Begoña Graña, Miguel Boudet, et al.
The American Journal of Gastroenterology
|
March 16, 2007
Attitudes toward prenatal genetic testing in patients with familial adenomatous polyposis
Fay Kastrinos, Elena M Stoffel, Judith Balmaña, et al.
Breast Cancer Research and Treatment
|
April 27, 2007
Detection of the CHEK2 1100delC mutation by MLPA BRCA1/2 analysis: a worthwhile strategy for its clinical applicability in 1100delC low-frequency populations?
Sara Gutiérrez-Enríquez, Judith Balmaña, Montserrat Baiget, et al.
Page
of 20