Theme: Hereditary Cancer Diseases IV.
Introductory word
Klin Onkol 2016; 29(Suppl 1): 3.
Authors: Foretová Lenka, Petráková Katarína2016-01-15:Editorial
Authors: Foretová Lenka, Petráková Katarína2016-01-15:Editorial
General
Klin Onkol 2016; 29(Suppl 1): 6-8.
2016-01-15:Seznam onkologických pracovišť a onkologů zajišťujících prevenci pro osoby (i zdravé) s dědičným rizikem nádorů. Seznam genetických ambulancí při KOC
2016-01-15:Seznam onkologických pracovišť a onkologů zajišťujících prevenci pro osoby (i zdravé) s dědičným rizikem nádorů. Seznam genetických ambulancí při KOC
Reviews
Klin Onkol 2016; 29(Suppl 1): 9-13.
DOI: 10.14735/amko2016S9.
Keywords: hereditary breast and ovarian cancer syndrome – genetic testing – genetic counseling
Authors: Foretová Lenka, Macháčková Eva, Palácová Markéta, Navrátilová Marie, Svoboda Marek, Petráková Katarína2016-01-15:Recommended Extension of Indication Criteria for Genetic Testing of BRCA1 and BRCA2 Mutations in Hereditary Breast and Ovarian Cancer Syndrome
Keywords: hereditary breast and ovarian cancer syndrome – genetic testing – genetic counseling
Authors: Foretová Lenka, Macháčková Eva, Palácová Markéta, Navrátilová Marie, Svoboda Marek, Petráková Katarína2016-01-15:Recommended Extension of Indication Criteria for Genetic Testing of BRCA1 and BRCA2 Mutations in Hereditary Breast and Ovarian Cancer Syndrome
Klin Onkol 2016; 29(Suppl 1): 14-21.
DOI: 10.14735/amko2016S14.
Keywords: hereditary breast and ovarian cancer syndrome – BRCA1 gene – BRCA2 gene – breast cancer – pancreatic cancer – prostate cancer – malignant melanoma
Authors: Petráková Katarína, Palácová Markéta, Schneiderová Monika, Standara Michal2016-01-15:Hereditary Breast and Ovarian Cancer Syndrome
Keywords: hereditary breast and ovarian cancer syndrome – BRCA1 gene – BRCA2 gene – breast cancer – pancreatic cancer – prostate cancer – malignant melanoma
Authors: Petráková Katarína, Palácová Markéta, Schneiderová Monika, Standara Michal2016-01-15:Hereditary Breast and Ovarian Cancer Syndrome
Gynecological Care and Prevention of Gynecological Malignancies in BRCA1 and BRCA2 Mutation Carriers
Klin Onkol 2016; 29(Suppl 1): 22-30.
DOI: 10.14735/amko2016S22.
Keywords: hereditary breast and ovarian cancer syndrome – ovarian neoplasms – BRCA1 gene – BRCA2 gene
Authors: Zikán Michal2016-01-15:Gynecological Care and Prevention of Gynecological Malignancies in BRCA1 and BRCA2 Mutation Carriers
Keywords: hereditary breast and ovarian cancer syndrome – ovarian neoplasms – BRCA1 gene – BRCA2 gene
Authors: Zikán Michal2016-01-15:Gynecological Care and Prevention of Gynecological Malignancies in BRCA1 and BRCA2 Mutation Carriers
Klin Onkol 2016; 29(Suppl 1): 55-61.
DOI: 10.14735/amko2016S55.
Keywords: colorectal cancer – colorectal tumorigenesis – Lynch syndrome – microsatellite instability – hypermethylation phenotype
Authors: Mlkvá Iveta2016-01-15:Genetics of Colorectal Tumorigenesis (Possibilities of Testing and Screening Prediction of Hereditary Form of Colorectal Cancer – Lynch Syndrome)
Keywords: colorectal cancer – colorectal tumorigenesis – Lynch syndrome – microsatellite instability – hypermethylation phenotype
Authors: Mlkvá Iveta2016-01-15:Genetics of Colorectal Tumorigenesis (Possibilities of Testing and Screening Prediction of Hereditary Form of Colorectal Cancer – Lynch Syndrome)
Klin Onkol 2016; 29(Suppl 1): 62-70.
DOI: 10.14735/amko2016S62.
Keywords: hereditary cancer predisposition syndromes – dysmorphology – pediatric cancer – genetic testing
Authors: Bajčiová Viera2016-01-15:Syndromes Predisposing to Cancer in Children – the Experience of Pediatric Oncology Department of University Hospital Brno
Keywords: hereditary cancer predisposition syndromes – dysmorphology – pediatric cancer – genetic testing
Authors: Bajčiová Viera2016-01-15:Syndromes Predisposing to Cancer in Children – the Experience of Pediatric Oncology Department of University Hospital Brno
Klin Onkol 2016; 29(Suppl 1): 71-77.
DOI: 10.14735/amko2016S71.
Keywords: brain tumours – child – hereditary cancer syndromes
Authors: Krutílková Věra2016-01-15:Genetic Syndromes Predisposing to Tumors of Central Nervous System in Children
Keywords: brain tumours – child – hereditary cancer syndromes
Authors: Krutílková Věra2016-01-15:Genetic Syndromes Predisposing to Tumors of Central Nervous System in Children
Klin Onkol 2016; 29(Suppl 1): 78-82.
DOI: 10.14735/amko2016S78.
Keywords: hepatoblastoma – α-fetoprotein – Beckwith-Wiedemann syndrome – APC-associated polyposis
Authors: Puchmajerová Alena, Křepelová Anna, Indráková Jana, Sítková Radka, Balaščák Ivan, Kruseová Jarmila, Švojgr Karel, Kodet Roman, Kynčl Martin, Vícha Aleš, Macek jr. Milan2016-01-15:Hepatoblastoma, Etiology, Case Reports
Keywords: hepatoblastoma – α-fetoprotein – Beckwith-Wiedemann syndrome – APC-associated polyposis
Authors: Puchmajerová Alena, Křepelová Anna, Indráková Jana, Sítková Radka, Balaščák Ivan, Kruseová Jarmila, Švojgr Karel, Kodet Roman, Kynčl Martin, Vícha Aleš, Macek jr. Milan2016-01-15:Hepatoblastoma, Etiology, Case Reports
Assisted Reproduction and Preimplantation Genetic Diagnosis in Patients Susceptible to Breast Cancer
Klin Onkol 2016; 29(Suppl 1): 93-99.
DOI: 10.14735/amko2016S93.
Keywords: breast neoplasms – hereditary cancer syndromes – assisted reproduction – ovarian reserve – hormonal stimulation – preimplantation diagnosis – karyomappin
Authors: Veselá Kateřina, Kocur Tomáš, Horák Jakub, Horňák Miroslav, Oráčová Eva, Hromadová Lenka, Veselý Jan, Trávník Pavel2016-01-15:Assisted Reproduction and Preimplantation Genetic Diagnosis in Patients Susceptible to Breast Cancer
Keywords: breast neoplasms – hereditary cancer syndromes – assisted reproduction – ovarian reserve – hormonal stimulation – preimplantation diagnosis – karyomappin
Authors: Veselá Kateřina, Kocur Tomáš, Horák Jakub, Horňák Miroslav, Oráčová Eva, Hromadová Lenka, Veselý Jan, Trávník Pavel2016-01-15:Assisted Reproduction and Preimplantation Genetic Diagnosis in Patients Susceptible to Breast Cancer
Original articles
Klin Onkol 2016; 29(Suppl 1): 31-34.
DOI: 10.14735/amko2016S31.
Keywords: hereditary breast and ovarian cancer syndrom – pancreatic neoplasms – PALB2 gene – genetic predisposition – genetic testing
Authors: Janatová Markéta, Borecká Marianna, Soukupová Jana, Kleiblová Petra, Stříbrná Jana, Vočka Michal, Zemánková Petra, Panczak Aleš, Veselá Kamila, Souček Pavel, Foretová Lenka, Kleibl Zdeněk2016-01-15:PALB2 as Another Candidate Gene for Genetic Testing in Patients with Hereditary Breast Cancer in Czech Republic
Keywords: hereditary breast and ovarian cancer syndrom – pancreatic neoplasms – PALB2 gene – genetic predisposition – genetic testing
Authors: Janatová Markéta, Borecká Marianna, Soukupová Jana, Kleiblová Petra, Stříbrná Jana, Vočka Michal, Zemánková Petra, Panczak Aleš, Veselá Kamila, Souček Pavel, Foretová Lenka, Kleibl Zdeněk2016-01-15: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
Klin Onkol 2016; 29(Suppl 1): 35-45.
DOI: 10.14735/amko2016S35.
Keywords: hereditary cancer syndromes – hereditary breast and ovarian cancer syndrome – hereditary nonpolyposis colorectal cancer – high-throughput DNA sequencing – TruSight cancer panel – MiSeq
Authors: Macháčková Eva, Házová Jana, Sťahlová Hrabincová Eva, Vašíčková Petra, Navrátilová Marie, Svoboda Marek, Foretová Lenka2016-01-15:Retrospective NGS Study in High-risk Hereditary Cancer Patients at Masaryk Memorial Cancer Institute
Keywords: hereditary cancer syndromes – hereditary breast and ovarian cancer syndrome – hereditary nonpolyposis colorectal cancer – high-throughput DNA sequencing – TruSight cancer panel – MiSeq
Authors: Macháčková Eva, Házová Jana, Sťahlová Hrabincová Eva, Vašíčková Petra, Navrátilová Marie, Svoboda Marek, Foretová Lenka2016-01-15:Retrospective NGS Study in High-risk Hereditary Cancer Patients at Masaryk Memorial Cancer Institute
Klin Onkol 2016; 29(Suppl 1): 46-54.
DOI: 10.14735/amko2016S46.
Keywords: genetic predisposition testing – hereditary cancer syndromes – high-throughput nucleotide sequencing – genetic information databases – panel sequencing – sequence capture – next-generation sequencing (NGS)
Authors: Soukupová Jana, Zemánková Petra, Kleiblová Petra, Janatová Markéta, Kleibl Zdeněk2016-01-15: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
Keywords: genetic predisposition testing – hereditary cancer syndromes – high-throughput nucleotide sequencing – genetic information databases – panel sequencing – sequence capture – next-generation sequencing (NGS)
Authors: Soukupová Jana, Zemánková Petra, Kleiblová Petra, Janatová Markéta, Kleibl Zdeněk2016-01-15: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
Case report
Klin Onkol 2016; 29(Suppl 1): 83-88.
DOI: 10.14735/amko2016S83.
Keywords: medulloblastoma – hereditary cancer syndromes – genetic testing – gene deletion – SUFU gene
Authors: Šoukalová Jana, Vejmělková Klára, Cermanová Tereza, Kašíková Kateřina, Mikulášová Aneta, Janyšková Helena, Melichárková Kristýna, Pavelka Zdeněk, Ježová Marta, Pospíšilová Šárka, Kuglík Petr, Valášková Iveta, Gaillyová Renata, Štěrba Jaroslav, Zitterbart Karel2016-01-15:Identification of a Family with SUFU Germline Deletion Based on a Case of Desmoplastic Medulloblastoma in an Infant
Keywords: medulloblastoma – hereditary cancer syndromes – genetic testing – gene deletion – SUFU gene
Authors: Šoukalová Jana, Vejmělková Klára, Cermanová Tereza, Kašíková Kateřina, Mikulášová Aneta, Janyšková Helena, Melichárková Kristýna, Pavelka Zdeněk, Ježová Marta, Pospíšilová Šárka, Kuglík Petr, Valášková Iveta, Gaillyová Renata, Štěrba Jaroslav, Zitterbart Karel2016-01-15:Identification of a Family with SUFU Germline Deletion Based on a Case of Desmoplastic Medulloblastoma in an Infant
Klin Onkol 2016; 29(Suppl 1): 89-92.
DOI: 10.14735/amko2016S89.
Keywords: Fanconi anemia – complementation group – FANCD1 – BRCA2 gene– leukemia – Wilms tumor – medulloblastoma
Authors: Puchmajerová Alena, Švojgr Karel, Novotná Drahuše, Macháčková Eva, Sumerauer David, Smíšek Petr, Kodet Roman, Kynčl Martin, Křepelová Anna, Foretová Lenka2016-01-15:Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene – Case Report
Keywords: Fanconi anemia – complementation group – FANCD1 – BRCA2 gene– leukemia – Wilms tumor – medulloblastoma
Authors: Puchmajerová Alena, Švojgr Karel, Novotná Drahuše, Macháčková Eva, Sumerauer David, Smíšek Petr, Kodet Roman, Kynčl Martin, Křepelová Anna, Foretová Lenka2016-01-15:Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene – Case Report
