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Search for publications relevant for "hereditary cancer"
hereditary cancer
Publication
Class
Person
Publication
Programmes
publication
Hereditary cancer syndromes
2003 |
First Faculty of Medicine
publication
Gynecological lesions in hereditary cancer predisposition syndromes
2021 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Family anamnesis relevance in pediatric oncolg care
2016 |
Faculty of Medicine in Pilsen
publication
Validation of CZECANCA (CZEch CAncer paNel for Clinical Application) for targeted NGS-based analysis of hereditary cancer syndromes
2018 |
First Faculty of Medicine
publication
Prerequisites for preimplantation genetic diagnosis (PGD in carriers of mutations responsible for hereditary cancers
2009 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Hereditary aetiology of cancer diseases and the importance of genetic counselling and testing in oncology
2006 |
Second Faculty of Medicine
publication
Risk factors of breast cancer - what is to fear and what is not
2012 |
First Faculty of Medicine
publication
Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort
2018 |
Second Faculty of Medicine
publication
Female Reproductive System and Cancer
2017 |
Publication without faculty affiliation
publication
The clinical importance of a genetic analysis of moderate-risk cancer susceptibility genes in breast and other cancer patients from the Czech Republic
2012 |
First Faculty of Medicine
publication
Breast cancer of young women- serious medical problem
2014 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Peutz-Jeghers syndrome
2021 |
Faculty of Medicine in Hradec Králové
publication
CHEK2 Germline Variants in Cancer Predisposition: Stalemate Rather than Checkmate
2020 |
First Faculty of Medicine
publication
CZECANCA: CZEch CAncer paNel for Clinical Application - Design and Optimization of the Targeted Sequencing Panel for the Identification of Cancer Susceptibility in High-risk Individuals from the Czech Republi
2016 |
First Faculty of Medicine
publication
Genetic analysis of subsequent second primary malignant neoplasms in long-term pancreatic cancer survivors suggests new potential hereditary genetic alterations
2019 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome?
2002 |
Second Faculty of Medicine
publication
Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, or Family Cancer History by NGS Analysis of 217 Genes
2020 |
First Faculty of Medicine, Central Library of Charles University
publication
Importance of Germline and Somatic Alterations in Human MRE11, RAD50, and NBN Genes Coding for MRN Complex
2023 |
First Faculty of Medicine, Faculty of Science
publication
Radiation-Induced Lymphopoenia and Treatment Outcome in Hereditary Breast Cancer Patients
2023 |
First Faculty of Medicine
publication
Fertility preservation and post-treatment pregnancies in post-pubertal cancer patients: ESMO Clinical Practice Guidelines
2020 |
Third Faculty of Medicine
publication
Hereditary breast cancer - new facts
2022 |
First Faculty of Medicine
publication
The changes and updates in the fifth edition of the WHO Classification of prostate tumors
2022 |
Faculty of Medicine in Pilsen
publication
Cases of LiFraumeni syndrome: diagnostic and preventive possibilities
2006 |
Second Faculty of Medicine
publication
Tumor suppressor genes
1997 |
Second Faculty of Medicine
publication
Prevalence of hereditary non-polyposis colorectal cancer (HNPCC) in Czech patients with endoscopic diagnosis of colorectal cancer
2001 |
Third Faculty of Medicine
publication
A solitary skeletal metastasis in the thumb of a silent bilateral clear cell renal cell carcinoma pT1a in a patient with a sporadic uro-oncological triplicity
2017 |
First Faculty of Medicine
publication
Broad genetic issues in lung cancer
2009 |
First Faculty of Medicine
publication
Li-Fraumeni syndrome - a proposal of complex prevention care for carriers of TP53 mutation with total-body MRI
2012 |
Second Faculty of Medicine
publication
Classification of germline variants identified in cancer predisposition genetic testing - consensus of the CZECANCA consortium
2023 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Early-Onset Ovarian Cancer <30 Years: What Do We Know about Its Genetic Predisposition?
2023 |
First Faculty of Medicine