Editorial
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Klin Onkol 2016; 29(Supplementum 1): 3
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Editorial
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Paediatric clinical oncology Surgery Clinical oncologyArticle was published in
Clinical Oncology
2016 Issue Supplementum 1
- Metamizole at a Glance and in Practice – Effective Non-Opioid Analgesic for All Ages
- Metamizole in perioperative treatment in children under 14 years – results of a questionnaire survey from practice
- Metamizole vs. Tramadol in Postoperative Analgesia
- The Importance of Hydration in Wound Healing
- Safety and Tolerance of Metamizole in Postoperative Analgesia in Children
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All articles in this issue
- Editorial
- Recommended Extension of Indication Criteria for Genetic Testing of BRCA1 and BRCA2 Mutations in Hereditary Breast and Ovarian Cancer Syndrome
- Hereditary Breast and Ovarian Cancer Syndrome
- Gynecological Care and Prevention of Gynecological Malignancies in BRCA1 and BRCA2 Mutation Carriers
- PALB2 as Another Candidate Gene for Genetic Testing in Patients with Hereditary Breast Cancer in Czech Republic
- Retrospective NGS Study in High-risk Hereditary Cancer Patients at Masaryk Memorial Cancer Institute
- 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 Republic
- Genetics of Colorectal Tumorigenesis (Possibilities of Testing and Screening Prediction of Hereditary Form of Colorectal Cancer – Lynch Syndrome)
- Syndromes Predisposing to Cancer in Children – the Experience of Pediatric Oncology Departmentof University Hospital Brno
- Genetic Syndromes Predisposing to Tumors of Central Nervous System in Children
- Hepatoblastoma, Etiology, Case Reports
- Identification of a Family with SUFU Germline Deletion Based on a Case of Desmoplastic Medulloblastoma in an Infant
- Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene – Case Report
- Clinical Oncology
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Most read in this issue
- PALB2 as Another Candidate Gene for Genetic Testing in Patients with Hereditary Breast Cancer in Czech Republic
- Hepatoblastoma, Etiology, Case Reports
- Genetics of Colorectal Tumorigenesis (Possibilities of Testing and Screening Prediction of Hereditary Form of Colorectal Cancer – Lynch Syndrome)
- Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene – Case Report