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Tytuł :
Prevalence of Pathogenic Germline BRCA1/2 Variants and Their Association with Clinical Characteristics in Patients with Epithelial Ovarian Cancer in a Rural Area of Japan.
Autorzy :
Abe A; Department of Gynecology, Cancer Institute Hospital of JCFR, Tokyo 135-8550, Japan.; Department of Obstetrics and Gynecology, Tokushima University, Tokushima 770-8503, Japan.
Imoto I; Aichi Cancer Center Research Institute, Nagoya 464-8681, Japan.
Tange S; Department of Medical Genome Sciences, Research Institute for Frontier Medicine, Sapporo Medical University, Sapporo 060-8556, Japan.
Nishimura M; Department of Obstetrics and Gynecology, Tokushima University, Tokushima 770-8503, Japan.
Iwasa T; Department of Obstetrics and Gynecology, Tokushima University, Tokushima 770-8503, Japan.
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Źródło :
Genes [Genes (Basel)] 2022 Jun 18; Vol. 13 (6). Date of Electronic Publication: 2022 Jun 18.
Typ publikacji :
Journal Article
MeSH Terms :
Carcinoma, Ovarian Epithelial*/diagnosis
Carcinoma, Ovarian Epithelial*/epidemiology
Carcinoma, Ovarian Epithelial*/genetics
Hereditary Breast and Ovarian Cancer Syndrome*
Ovarian Neoplasms*/diagnosis
Ovarian Neoplasms*/epidemiology
Ovarian Neoplasms*/genetics
BRCA1 Protein/genetics ; BRCA2 Protein/genetics ; Female ; Germ Cells ; Germ-Line Mutation ; Humans ; Japan/epidemiology ; Prevalence
Czasopismo naukowe
Tytuł :
Genetic medicine is accelerating in Japan.
Autorzy :
Hayashi S; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi Higashi-ku, Fukuoka, 812-8582, Japan.; Department of Clinical Genetics and Medicine, Kyushu University Hospital, Fukuoka, Japan.
Kubo M; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi Higashi-ku, Fukuoka, 812-8582, Japan. .; Department of Clinical Genetics and Medicine, Kyushu University Hospital, Fukuoka, Japan. .
Kaneshiro K; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi Higashi-ku, Fukuoka, 812-8582, Japan.
Kai M; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi Higashi-ku, Fukuoka, 812-8582, Japan.
Yamada M; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi Higashi-ku, Fukuoka, 812-8582, Japan.
Morisaki T; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi Higashi-ku, Fukuoka, 812-8582, Japan.
Takao Y; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi Higashi-ku, Fukuoka, 812-8582, Japan.
Shimazaki A; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi Higashi-ku, Fukuoka, 812-8582, Japan.
Shikada S; Department of Clinical Genetics and Medicine, Kyushu University Hospital, Fukuoka, Japan.
Nakamura M; Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi Higashi-ku, Fukuoka, 812-8582, Japan.
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Źródło :
Breast cancer (Tokyo, Japan) [Breast Cancer] 2022 Jul; Vol. 29 (4), pp. 659-665. Date of Electronic Publication: 2022 Feb 21.
Typ publikacji :
Journal Article
MeSH Terms :
Breast Neoplasms*/genetics
Hereditary Breast and Ovarian Cancer Syndrome*/genetics
Ovarian Neoplasms*/diagnosis
Triple Negative Breast Neoplasms*/genetics
BRCA1 Protein/genetics ; BRCA2 Protein/genetics ; Female ; Genetic Testing ; Humans ; Japan
Czasopismo naukowe
Tytuł :
Cancer genetics and breast cancer.
Autorzy :
Huber-Keener KJ; University of Iowa Hospitals and Clinics, Department of Obstetrics & Gynecology, 200 Hawkins Drive, Iowa City, IA, USA. Electronic address: .
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Źródło :
Best practice & research. Clinical obstetrics & gynaecology [Best Pract Res Clin Obstet Gynaecol] 2022 Jun; Vol. 82, pp. 3-11. Date of Electronic Publication: 2022 Jan 31.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Breast Neoplasms*/genetics
Hereditary Breast and Ovarian Cancer Syndrome*/genetics
Female ; Genetic Predisposition to Disease ; Germ-Line Mutation ; Humans
SCR Disease Name :
Breast Cancer, Familial
Czasopismo naukowe
Tytuł :
Advocating for equitable management of hereditary cancer syndromes.
Autorzy :
Caffrey RG; Advocate Lutheran General Hospital, Advocate Aurora Health, Park Ridge, USA.
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Źródło :
Journal of genetic counseling [J Genet Couns] 2022 Jun; Vol. 31 (3), pp. 584-589. Date of Electronic Publication: 2022 Jan 14.
Typ publikacji :
Journal Article
MeSH Terms :
Hereditary Breast and Ovarian Cancer Syndrome*/genetics
Neoplastic Syndromes, Hereditary*/diagnosis
Neoplastic Syndromes, Hereditary*/genetics
Neoplastic Syndromes, Hereditary*/therapy
Female ; Genetic Counseling ; Genetic Testing ; Humans ; Precision Medicine
Czasopismo naukowe
Tytuł :
BRCA1/2 variants of unknown significance in hereditary breast and ovarian cancer (HBOC) syndrome: Looking for the hidden meaning.
Autorzy :
Fanale D; Section of Medical Oncology, Department of Surgical, Oncological and Oral Sciences, University of Palermo, 90127 Palermo, Italy.
Pivetti A; Section of Medical Oncology, Department of Surgical, Oncological and Oral Sciences, University of Palermo, 90127 Palermo, Italy.
Cancelliere D; Section of Medical Oncology, Department of Surgical, Oncological and Oral Sciences, University of Palermo, 90127 Palermo, Italy.
Spera A; Department of Radiotherapy, San Giovanni di Dio Hospital, ASP of Agrigento, Agrigento, Italy.
Bono M; Section of Medical Oncology, Department of Surgical, Oncological and Oral Sciences, University of Palermo, 90127 Palermo, Italy.
Fiorino A; Section of Medical Oncology, Department of Surgical, Oncological and Oral Sciences, University of Palermo, 90127 Palermo, Italy.
Pedone E; Section of Medical Oncology, Department of Surgical, Oncological and Oral Sciences, University of Palermo, 90127 Palermo, Italy.
Barraco N; Section of Medical Oncology, Department of Surgical, Oncological and Oral Sciences, University of Palermo, 90127 Palermo, Italy.
Brando C; Section of Medical Oncology, Department of Surgical, Oncological and Oral Sciences, University of Palermo, 90127 Palermo, Italy.
Perez A; Section of Medical Oncology, Department of Surgical, Oncological and Oral Sciences, University of Palermo, 90127 Palermo, Italy.
Guarneri MF; Azienda Sanitaria Provinciale of Palermo, Palermo, Italy.
Russo TDB; Section of Medical Oncology, Department of Surgical, Oncological and Oral Sciences, University of Palermo, 90127 Palermo, Italy.
Vieni S; Division of General and Oncological Surgery, Department of Surgical, Oncological and Oral Sciences, University of Palermo, Italy.
Guarneri G; Gynecology Section, Mother - Child Department, University of Palermo, 90127 Palermo, Italy.
Russo A; Section of Medical Oncology, Department of Surgical, Oncological and Oral Sciences, University of Palermo, 90127 Palermo, Italy. Electronic address: .
Bazan V; Department of Biomedicine, Neuroscience and Advanced Diagnostics, University of Palermo, 90127 Palermo, Italy.
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Źródło :
Critical reviews in oncology/hematology [Crit Rev Oncol Hematol] 2022 Apr; Vol. 172, pp. 103626. Date of Electronic Publication: 2022 Feb 10.
Typ publikacji :
Journal Article; Review
MeSH Terms :
BRCA1 Protein*/genetics
BRCA2 Protein*/genetics
Breast Neoplasms*/genetics
Hereditary Breast and Ovarian Cancer Syndrome*/diagnosis
Hereditary Breast and Ovarian Cancer Syndrome*/genetics
Ovarian Neoplasms*/genetics
Female ; Genetic Predisposition to Disease ; Germ-Line Mutation ; Humans ; Mutation ; Risk Assessment
Czasopismo naukowe
Tytuł :
Hereditary Breast and Ovarian Cancer: An Updated Primer for OB/GYNs.
Autorzy :
Bellcross CA; Emory University School of Medicine, 1462 Clifton Road, Suite 310, MS 1370-003-1AE, Atlanta, GA 30322, USA. Electronic address: .
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Źródło :
Obstetrics and gynecology clinics of North America [Obstet Gynecol Clin North Am] 2022 Mar; Vol. 49 (1), pp. 117-147.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Breast Neoplasms*/diagnosis
Breast Neoplasms*/genetics
Gynecology*
Hereditary Breast and Ovarian Cancer Syndrome*/diagnosis
Hereditary Breast and Ovarian Cancer Syndrome*/genetics
Ovarian Neoplasms*/diagnosis
Ovarian Neoplasms*/genetics
Female ; Genetic Predisposition to Disease ; Genetic Testing ; Humans
Czasopismo naukowe
Tytuł :
Factors influencing genetic counseling and testing for hereditary breast and ovarian cancer syndrome in a large US health care system.
Autorzy :
Powell CB; Kaiser Permanente Northern California, Division of Research, Oakland, California, USA.; Kaiser Permanente Northern California Hereditary Cancer Program San Francisco, Oakland, California, USA.
Laurent C; Kaiser Permanente Northern California, Division of Research, Oakland, California, USA.
Garcia C; Kaiser Permanente Northern California Hereditary Cancer Program San Francisco, Oakland, California, USA.
Hoodfar E; Kaiser Permanente Northern California Hereditary Cancer Program San Francisco, Oakland, California, USA.; Kaiser Permanente Northern California Genetics Department, Oakland, California, USA.
Karlea A; Kaiser Permanente Northern California Hereditary Cancer Program San Francisco, Oakland, California, USA.; Kaiser Permanente Northern California Genetics Department, Oakland, California, USA.
Kobelka C; Kaiser Permanente Northern California Hereditary Cancer Program San Francisco, Oakland, California, USA.; Kaiser Permanente Northern California Genetics Department, Oakland, California, USA.
Lee J; Kaiser Permanente Oakland Obstetrics and Gynecology Residency Program, Oakland, California, USA.
Roh J; Kaiser Permanente Northern California, Division of Research, Oakland, California, USA.
Kushi LH; Kaiser Permanente Northern California, Division of Research, Oakland, California, USA.
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Źródło :
Clinical genetics [Clin Genet] 2022 Mar; Vol. 101 (3), pp. 324-334. Date of Electronic Publication: 2021 Dec 27.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Breast Neoplasms*/diagnosis
Breast Neoplasms*/epidemiology
Breast Neoplasms*/genetics
Hereditary Breast and Ovarian Cancer Syndrome*/diagnosis
Hereditary Breast and Ovarian Cancer Syndrome*/epidemiology
Hereditary Breast and Ovarian Cancer Syndrome*/genetics
Ovarian Neoplasms*/diagnosis
Ovarian Neoplasms*/epidemiology
Ovarian Neoplasms*/genetics
Delivery of Health Care ; Female ; Genetic Counseling/psychology ; Genetic Predisposition to Disease ; Genetic Testing ; Humans ; Male
Czasopismo naukowe
Tytuł :
Pancreatic Cancer with Mutation in BRCA1/2, MLH1, and APC Genes: Phenotype Correlation and Detection of a Novel Germline BRCA2 Mutation.
Autorzy :
Vietri MT; Department of Precision Medicine, University of Campania 'Luigi Vanvitelli', 80138 Naples, Italy.; Unity of Clinical and Molecular Pathology, AOU, University of Campania 'Luigi Vanvitelli', 80138 Naples, Italy.
D'Elia G; Unity of Clinical and Molecular Pathology, AOU, University of Campania 'Luigi Vanvitelli', 80138 Naples, Italy.
Caliendo G; Unity of Clinical and Molecular Pathology, AOU, University of Campania 'Luigi Vanvitelli', 80138 Naples, Italy.
Albanese L; Unity of Clinical and Molecular Pathology, AOU, University of Campania 'Luigi Vanvitelli', 80138 Naples, Italy.
Signoriello G; Statistical Unit, Department of Precision Medicine, University of Campania 'Luigi Vanvitelli', 80138 Naples, Italy.
Napoli C; Department of Advanced Medical and Surgical Sciences (DAMSS), University of Campania 'Luigi Vanvitelli', 80138 Naples, Italy.; Clinical Department of Internal Medicine and Specialistic Units, AOU, University of Campania 'Luigi Vanvitelli', 80138 Naples, Italy.
Molinari AM; Department of Precision Medicine, University of Campania 'Luigi Vanvitelli', 80138 Naples, Italy.; Unity of Clinical and Molecular Pathology, AOU, University of Campania 'Luigi Vanvitelli', 80138 Naples, Italy.
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Źródło :
Genes [Genes (Basel)] 2022 Feb 09; Vol. 13 (2). Date of Electronic Publication: 2022 Feb 09.
Typ publikacji :
Journal Article
MeSH Terms :
Adenomatous Polyposis Coli*/genetics
Carcinoma, Pancreatic Ductal*/genetics
Colorectal Neoplasms, Hereditary Nonpolyposis*/genetics
Hereditary Breast and Ovarian Cancer Syndrome*/genetics
Pancreatic Neoplasms*/genetics
Adenomatous Polyposis Coli Protein ; BRCA1 Protein/genetics ; BRCA2 Protein ; Female ; Genes, APC ; Germ Cells ; Humans ; MutL Protein Homolog 1/genetics ; Mutation ; Phenotype
SCR Disease Name :
Pancreatic Carcinoma
Czasopismo naukowe
Tytuł :
BRCA1/2 Mutations in Vietnamese Patients with Hereditary Breast and Ovarian Cancer Syndrome.
Autorzy :
Le TN; Hanoi Medical University, Hanoi 100000, Vietnam.
Tran VK; Hanoi Medical University, Hanoi 100000, Vietnam.
Nguyen TT; Hanoi Medical University, Hanoi 100000, Vietnam.
Vo NS; Center for Biomedical Informatics, Vingroup Big Data Institute, Hanoi 100000, Vietnam.
Hoang TH; Center for Biomedical Informatics, Vingroup Big Data Institute, Hanoi 100000, Vietnam.
Vo HL; Hanoi Medical University, Hanoi 100000, Vietnam.
Nguyen TT; Hanoi Medical University, Hanoi 100000, Vietnam.
Nguyen PD; National Institute of Hematology and Blood Transfusion, Hanoi 100000, Vietnam.
Nguyen VT; Hanoi Medical University, Hanoi 100000, Vietnam.
Ta TV; Hanoi Medical University, Hanoi 100000, Vietnam.; Hanoi Medical University Hospital, Hanoi Medical University, Hanoi 100000, Vietnam.
Tran HT; Hanoi Medical University, Hanoi 100000, Vietnam.; Hanoi Medical University Hospital, Hanoi Medical University, Hanoi 100000, Vietnam.
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Źródło :
Genes [Genes (Basel)] 2022 Jan 29; Vol. 13 (2). Date of Electronic Publication: 2022 Jan 29.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Hereditary Breast and Ovarian Cancer Syndrome*/epidemiology
Hereditary Breast and Ovarian Cancer Syndrome*/genetics
Ovarian Neoplasms*/epidemiology
Ovarian Neoplasms*/genetics
Ovarian Neoplasms*/pathology
BRCA1 Protein/genetics ; Female ; Genetic Predisposition to Disease ; Humans ; Mutation ; Vietnam/epidemiology
Czasopismo naukowe
Tytuł :
Increasing referral of at-risk women for genetic counseling and BRCA testing using a screening tool in a community breast imaging center.
Autorzy :
Arun BK; Department of Breast Medical Oncology and Clinical Cancer Genetics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Peterson SK; Department of Behavioral Science, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Sweeney LE; Houston Breast Screening Network, Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Bluebond RD; Department of Clinical Cancer Genetics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Tidwell RSS; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Makhnoon S; Department of Behavioral Science, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Kushwaha AC; Houston Breast Screening Network, Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
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Źródło :
Cancer [Cancer] 2022 Jan 01; Vol. 128 (1), pp. 94-102. Date of Electronic Publication: 2021 Aug 23.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Breast Neoplasms*/diagnostic imaging
Breast Neoplasms*/genetics
Hereditary Breast and Ovarian Cancer Syndrome*/diagnosis
Hereditary Breast and Ovarian Cancer Syndrome*/genetics
Ovarian Neoplasms*/diagnostic imaging
Ovarian Neoplasms*/genetics
Female ; Genes, BRCA2 ; Genetic Counseling ; Genetic Predisposition to Disease ; Genetic Testing ; Humans ; Mutation ; Referral and Consultation
Czasopismo naukowe
Tytuł :
Hereditary breast and ovarian cancer (HBOC): review of its molecular characteristics, screening, treatment, and prognosis.
Autorzy :
Yoshida R; Showa University Advanced Cancer Translational Research Institute, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8555, Japan. .
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Źródło :
Breast cancer (Tokyo, Japan) [Breast Cancer] 2021 Nov; Vol. 28 (6), pp. 1167-1180. Date of Electronic Publication: 2020 Aug 29.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Genetic Predisposition to Disease*
Hereditary Breast and Ovarian Cancer Syndrome/*genetics
BRCA1 Protein ; BRCA2 Protein ; Female ; Hereditary Breast and Ovarian Cancer Syndrome/pathology ; Hereditary Breast and Ovarian Cancer Syndrome/therapy ; Humans ; Male ; Mutation ; Risk Assessment
Czasopismo naukowe
Tytuł :
Clinical Contribution of Next-Generation Sequencing Multigene Panel Testing for BRCA Negative High-Risk Patients With Breast Cancer.
Autorzy :
Ece Solmaz A; Department of Medical Genetic, Ege University Faculty of Medicine, Izmir, Turkey. Electronic address: .
Yeniay L; Department of General Surgery, Ege University Faculty of Medicine, Izmir, Turkey.
Gökmen E; Department of Medical Oncology, Ege University Faculty of Medicine, Izmir, Turkey.
Zekioğlu O; Department of Pathology, Ege University Faculty of Medicine, Izmir, Turkey.
Haydaroğlu A; Department of Radiation Oncology, Ege University Faculty of Medicine, Izmir, Turkey.
Bilgen I; Department of Radiology, Ege University Faculty of Medicine, Izmir, Turkey.
Özkınay F; Department of Medical Genetic, Ege University Faculty of Medicine, Izmir, Turkey.
Onay H; Department of Medical Genetic, Ege University Faculty of Medicine, Izmir, Turkey.
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Źródło :
Clinical breast cancer [Clin Breast Cancer] 2021 Dec; Vol. 21 (6), pp. e647-e653. Date of Electronic Publication: 2021 Apr 12.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
High-Throughput Nucleotide Sequencing*
BRCA1 Protein/*genetics
Breast Neoplasms/*genetics
Hereditary Breast and Ovarian Cancer Syndrome/*genetics
Adult ; Breast Neoplasms/diagnosis ; Female ; Hereditary Breast and Ovarian Cancer Syndrome/diagnosis ; Humans ; Middle Aged ; Mutation ; Retrospective Studies ; Turkey
SCR Disease Name :
Breast Cancer, Familial
Czasopismo naukowe
Tytuł :
[Comparison of hereditary breast and ovarian cancer syndrome and sporadic ovarian cancer in ovarian cancer BRCA mutations].
Autorzy :
Duan RR; Department of Obstetrics and Gynecology, Graduate School, Shanxi Medical University, Taiyuan 030000, China.
Sun LX; Department of Gynecology, Shanxi Provincial Cancer Hospital, Taiyuan 030000, China.
Zhao HW; Department of Gynecology, Shanxi Provincial Cancer Hospital, Taiyuan 030000, China.
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Źródło :
Zhonghua fu chan ke za zhi [Zhonghua Fu Chan Ke Za Zhi] 2021 Nov 25; Vol. 56 (11), pp. 788-795.
Typ publikacji :
Journal Article
MeSH Terms :
Breast Neoplasms*/genetics
Hereditary Breast and Ovarian Cancer Syndrome*/genetics
Ovarian Neoplasms*/genetics
BRCA1 Protein/genetics ; BRCA2 Protein/genetics ; Female ; Genes, BRCA2 ; Genetic Predisposition to Disease ; Humans ; Mutation
Czasopismo naukowe
Tytuł :
The Importance of Extended Analysis Using Current Molecular Genetic Methods Based on the Example of a Cohort of 228 Patients with Hereditary Breast and Ovarian Cancer Syndrome.
Autorzy :
Resch LD; Medical Center, Faculty of Medicine, Institute of Human Genetics, University of Freiburg, 79106 Freiburg, Germany.
Hotz A; Medical Center, Faculty of Medicine, Institute of Human Genetics, University of Freiburg, 79106 Freiburg, Germany.
Zimmer AD; Medical Center, Faculty of Medicine, Institute of Human Genetics, University of Freiburg, 79106 Freiburg, Germany.
Komlosi K; Medical Center, Faculty of Medicine, Institute of Human Genetics, University of Freiburg, 79106 Freiburg, Germany.
Singh N; Medical Center, Faculty of Medicine, Institute of Human Genetics, University of Freiburg, 79106 Freiburg, Germany.
Tzschach A; Medical Center, Faculty of Medicine, Institute of Human Genetics, University of Freiburg, 79106 Freiburg, Germany.
Windfuhr-Blum M; Radiology, Medical Center, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany.
Juhasz-Boess I; Department of Obstetrics and Gynaecology, Medical Center, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany.
Erbes T; Department of Obstetrics and Gynaecology, Medical Center, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany.
Fischer J; Medical Center, Faculty of Medicine, Institute of Human Genetics, University of Freiburg, 79106 Freiburg, Germany.
Alter S; Medical Center, Faculty of Medicine, Institute of Human Genetics, University of Freiburg, 79106 Freiburg, Germany.
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Źródło :
Genes [Genes (Basel)] 2021 Sep 24; Vol. 12 (10). Date of Electronic Publication: 2021 Sep 24.
Typ publikacji :
Journal Article
MeSH Terms :
Pathology, Molecular*
BRCA1 Protein/*genetics
BRCA2 Protein/*genetics
Hereditary Breast and Ovarian Cancer Syndrome/*diagnosis
Female ; Genetic Predisposition to Disease ; Genetic Testing ; Germ-Line Mutation/genetics ; Hereditary Breast and Ovarian Cancer Syndrome/epidemiology ; Hereditary Breast and Ovarian Cancer Syndrome/genetics ; High-Throughput Nucleotide Sequencing ; Humans ; Male ; Middle Aged ; Neoplasm Proteins/genetics ; Risk Factors
Czasopismo naukowe
Tytuł :
Surgical Management of Hereditary Breast Cancer.
Autorzy :
Berger ER; Department of Surgery, School of Medicine, Yale University, New Haven, CT 06511, USA.
Golshan M; Department of Surgery, School of Medicine, Yale University, New Haven, CT 06511, USA.
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Źródło :
Genes [Genes (Basel)] 2021 Aug 31; Vol. 12 (9). Date of Electronic Publication: 2021 Aug 31.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Breast Neoplasms/*therapy
Hereditary Breast and Ovarian Cancer Syndrome/*therapy
Mastectomy/*standards
Prophylactic Surgical Procedures/*standards
Salpingo-oophorectomy/*standards
Antineoplastic Agents/therapeutic use ; BRCA1 Protein/genetics ; BRCA2 Protein/genetics ; Breast Neoplasms/diagnosis ; Breast Neoplasms/genetics ; Chemoprevention/methods ; Chemoprevention/standards ; Female ; Genetic Predisposition to Disease ; Genetic Testing/standards ; Hereditary Breast and Ovarian Cancer Syndrome/diagnosis ; Hereditary Breast and Ovarian Cancer Syndrome/genetics ; Heterozygote ; Humans ; Mastectomy/methods ; Mutation ; Practice Guidelines as Topic ; Prophylactic Surgical Procedures/methods ; Salpingo-oophorectomy/methods
SCR Disease Name :
Breast Cancer, Familial
Czasopismo naukowe
Tytuł :
Hereditary Breast and Ovarian Cancer Screening Syndrome Profile in Women Diagnosed with Breast Cancer from Paraná State Southwest.
Autorzy :
Moura JB; Laboratory of Tumor Biology, Universidade do Estado do Paraná, Francisco Beltrão, PR, Brazil.
Ghedin CC; Laboratory of Tumor Biology, Universidade do Estado do Paraná, Francisco Beltrão, PR, Brazil.
Takakura ÉT; Laboratory of Tumor Biology, Universidade do Estado do Paraná, Francisco Beltrão, PR, Brazil.
Scandolara TB; Laboratory of Tumor Biology, Universidade do Estado do Paraná, Francisco Beltrão, PR, Brazil.; Department of Genetics, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Rech D; Center of Health Sciences, Francisco Beltrão Cancer Hospital, Francisco Beltrão, PR, Brazil.
Panis C; Laboratory of Tumor Biology, Universidade do Estado do Paraná, Francisco Beltrão, PR, Brazil.
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Transliterated Title :
Perfil do rastreamento da síndrome hereditária de câncer de mama e ovário em mulheres diagnosticadas com câncer de mama na região sudoeste do Paraná.
Źródło :
Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia [Rev Bras Ginecol Obstet] 2021 Aug; Vol. 43 (8), pp. 616-621. Date of Electronic Publication: 2021 Sep 21.
Typ publikacji :
Journal Article
MeSH Terms :
Breast Neoplasms*/diagnosis
Breast Neoplasms*/genetics
Hereditary Breast and Ovarian Cancer Syndrome*
Ovarian Neoplasms*/diagnosis
Ovarian Neoplasms*/genetics
Early Detection of Cancer ; Female ; Genetic Predisposition to Disease ; Humans ; Mass Screening
Czasopismo naukowe
Tytuł :
Trends and timing of risk-reducing mastectomy uptake in unaffected BRCA1 and BRCA2 carriers in Slovenia.
Autorzy :
Ložar T; University of Ljubljana, Slovenia; Department of Surgical Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Žgajnar J; University of Ljubljana, Slovenia; Department of Surgical Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Perhavec A; University of Ljubljana, Slovenia; Department of Surgical Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Blatnik A; University of Ljubljana, Slovenia; Cancer Genetics Clinic, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Novaković S; Department of Molecular Diagnostics, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Krajc M; University of Ljubljana, Slovenia; Cancer Genetics Clinic, Institute of Oncology Ljubljana, Ljubljana, Slovenia. Electronic address: .
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Źródło :
European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology [Eur J Surg Oncol] 2021 Aug; Vol. 47 (8), pp. 1900-1906. Date of Electronic Publication: 2021 Mar 26.
Typ publikacji :
Journal Article
MeSH Terms :
Genes, BRCA1*
Genes, BRCA2*
Hereditary Breast and Ovarian Cancer Syndrome/*prevention & control
Prophylactic Mastectomy/*trends
Salpingo-oophorectomy/*trends
Adult ; Aged ; Aged, 80 and over ; Breast Neoplasms/epidemiology ; Female ; Hereditary Breast and Ovarian Cancer Syndrome/genetics ; Heterozygote ; Humans ; Middle Aged ; Prophylactic Mastectomy/statistics & numerical data ; Prophylactic Surgical Procedures/statistics & numerical data ; Prophylactic Surgical Procedures/trends ; Salpingo-oophorectomy/statistics & numerical data ; Slovenia ; Time Factors ; Undiagnosed Diseases/epidemiology
Czasopismo naukowe
Tytuł :
Framing Effects on Decision-Making for Diagnostic Genetic Testing: Results from a Randomized Trial.
Autorzy :
Dwyer AA; William F. Connell School of Nursing, Boston College, Chestnut Hill, MA 02467, USA.; Massachusetts General Hospital-Harvard Center for Reproductive Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.
Shen H; Department of Measurement, Evaluation, Statistics and Assessment, Lynch School of Education, Boston College, Chestnut Hill, MA 02467, USA.
Zeng Z; Department of Measurement, Evaluation, Statistics and Assessment, Lynch School of Education, Boston College, Chestnut Hill, MA 02467, USA.
Gregas M; Department of Research Services, Boston College, Chestnut Hill, MA 02467, USA.
Zhao M; Carroll School of Management, Boston College, Chestnut Hill, MA 02467, USA.
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Źródło :
Genes [Genes (Basel)] 2021 Jun 20; Vol. 12 (6). Date of Electronic Publication: 2021 Jun 20.
Typ publikacji :
Journal Article; Randomized Controlled Trial; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Choice Behavior*
Genetic Testing*
Patient Preference*
Genetic Counseling/*psychology
Hereditary Breast and Ovarian Cancer Syndrome/*genetics
Hypogonadism/*genetics
Adult ; Female ; Hereditary Breast and Ovarian Cancer Syndrome/diagnosis ; Hereditary Breast and Ovarian Cancer Syndrome/psychology ; Humans ; Hypogonadism/diagnosis ; Hypogonadism/psychology ; Male ; Middle Aged ; Patient Education as Topic
Czasopismo naukowe

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