Search Results - "Espenschied, C"
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271 Vulvoscopic Findings, Patient Reported Outcome (Pro) Measures, and Hormonal Blood Test Values in Menopausal Women With Female Sexual Dysfunction Pre- and Post-Hormonal Treatment: A Retrospective Single Center Study
Published in Journal of sexual medicine (01-01-2017)Get full text
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Classifying variants in the CHEK2 gene: the importance of collaboration
Published in European journal of cancer (1990) (01-02-2017)Get full text
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Abstract PD1-11: Moderate risk genes matter: Multigene testing for hereditary breast cancer
Published in Cancer research (Chicago, Ill.) (15-02-2018)“…Abstract Background: Many genes have been associated with hereditary breast cancer (BC). For some genes, the associated cancer risks have been debated;…”
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Abstract P2-02-05: Comparison of non-breast and ovarian cancer phenotypes of BRCA1/2 mutation carriers across multi-gene panels
Published in Cancer research (Chicago, Ill.) (15-02-2017)“…Abstract Background: BRCA1/2 germline mutations account for the majority of hereditary breast and ovarian cancers. Until 2013, the only way to identify…”
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050 Lifetime Persistent Genital Arousal Disorder: Management of PGAD in an Adolescent
Published in Journal of sexual medicine (01-06-2016)Get full text
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016 Vulvoscopic Findings, Patient Reported Outcome (PRO) Measures, and Hormonal Blood Test Values in Menopausal Women with Female Sexual Dysfunction Pre- and Post-Hormonal Treatment: A Retrospective Single Center Study
Published in Journal of sexual medicine (01-06-2016)Get full text
Journal Article -
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208 - Classifying variants in the CHEK2 gene: the importance of collaboration
Published in European journal of cancer (1990) (01-02-2017)Get full text
Journal Article -
8
Abstract P2-02-07: Predicting germline mutations in BRCA1/2 and beyond: A comparison of women with single and multiple breast primaries
Published in Cancer research (Chicago, Ill.) (15-02-2017)“…Abstract Synchronous or metachronous breast primaries are a well-known indication of hereditary breast cancer, particularly within BRCA1/2 mutation carriers…”
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