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Tytuł:
Feasibility of cancer genetic counselling and screening in Cameroon: perceived benefits and barriers.
Autorzy:
Mapoko, Berthe Sabine Esson
Kenn Chi Ndi
Tabola, Lionel
Mouaye, Vanessa
Douanla, Pelagie
Nsangou, Nasser
Nkeng, Glenda
Vanvolkenburgh, Carmen
Dzekem, Bonaventure
Dezheng Huo
Ndom, Paul
Olopade, Olufunmilayo
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Źródło:
Ecancermedicalscience. 2023, Vol. 17 Issue 1588-1650, p1-21. 21p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Cost-effectiveness of bringing a nurse into an Italian genetic day clinic: a before and after study.
Autorzy:
Mordenti, Marina (AUTHOR)
Tremosini, Morena (AUTHOR)
Locatelli, Manuela (AUTHOR)
Gnoli, Maria (AUTHOR)
Forni, Cristiana (AUTHOR)
Pedrini, Elena (AUTHOR)
Boarini, Manila (AUTHOR)
Sangiorgi, Luca (AUTHOR)
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Źródło:
BMC Health Services Research. 11/20/2023, Vol. 23 Issue 1, p1-9. 9p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Evidence‐based consensus guidelines for ALS genetic testing and counseling.
Autorzy:
Roggenbuck, Jennifer (AUTHOR)
Eubank, Breda H. F. (AUTHOR)
Wright, Joshua (AUTHOR)
Harms, Matthew B. (AUTHOR)
Kolb, Stephen J. (AUTHOR)
Ajroud‐Driss, Senda (AUTHOR)
Arcila Londono, Ximena (AUTHOR)
Bauer, Gregory (AUTHOR)
Benatar, Michael (AUTHOR)
Bedlack, Richard (AUTHOR)
Brooks, Benjamin Rix (AUTHOR)
Chambers, Chelsea (AUTHOR)
Chehab, Farid F. (AUTHOR)
Dratch, Laynie (AUTHOR)
Harrington, Elizabeth A. (AUTHOR)
Elman, Lauren (AUTHOR)
Fernandes, Joseph Americo (AUTHOR)
Foster, Laura (AUTHOR)
Jackson, Carlayne E. (AUTHOR)
Fong, Jamie C. (AUTHOR)
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Źródło:
Annals of Clinical & Translational Neurology. Nov2023, Vol. 10 Issue 11, p2074-2091. 18p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Novel compound heterozygous mutations of MTHFR Gene in a Chinese family with homocystinuria due to MTHFR deficiency.
Autorzy:
Lu Y; Xi'an People's Hospital (Xi'an Fourth Hospital), Xi'an, China.
Zhao S; Xi'an People's Hospital (Xi'an Fourth Hospital), Xi'an, China.
He X; Xi'an People's Hospital (Xi'an Fourth Hospital), Xi'an, China.
Yang H; Xi'an People's Hospital (Xi'an Fourth Hospital), Xi'an, China.
Wang X; Xi'an People's Hospital (Xi'an Fourth Hospital), Xi'an, China.
Miao C; Xi'an People's Hospital (Xi'an Fourth Hospital), Xi'an, China.
Liu H; Xi'an People's Hospital (Xi'an Fourth Hospital), Xi'an, China.
Zhang X; Xi'an People's Hospital (Xi'an Fourth Hospital), Xi'an, China. .
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Źródło:
BMC medical genomics [BMC Med Genomics] 2022 Dec 25; Vol. 15 (1), pp. 271. Date of Electronic Publication: 2022 Dec 25.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Counseling*
Homocystinuria*/genetics
Homocystinuria*/complications
Methylenetetrahydrofolate Reductase (NADPH2)*/genetics
Heterozygote*
Female ; Humans ; Male ; Pregnancy ; East Asian People ; Mutation ; Pedigree
SCR Disease Name:
Methylenetetrahydrofolate reductase deficiency
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Referral, Genetic Counselling, and BRCA Testing in the Manitoba High-Grade Serous Ovarian Cancer Population, 2004-2019.
Autorzy:
Winchar K; Obstetrics, Gynecology and Reproductive Sciences, University of Manitoba, Winnipeg, MB R3A 1R9, Canada.
Lambert P; CancerCare Manitoba Research Institute, CancerCare Manitoba, Winnipeg, MB R3E OV9, Canada.; Epidemiology and Cancer Registry, CancerCare Manitoba, Winnipeg, MB R3E OV9, Canada.
McManus KJ; CancerCare Manitoba Research Institute, CancerCare Manitoba, Winnipeg, MB R3E OV9, Canada.; Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, MB R3E OV9, Canada.
Chodirker B; Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, MB R3E OV9, Canada.; Pediatrics and Child Health (Section of Genetics and Metabolism), University of Manitoba, Winnipeg, MB R3E OV9, Canada.
Kean S; Obstetrics, Gynecology and Reproductive Sciences, University of Manitoba, Winnipeg, MB R3A 1R9, Canada.
Serfas K; Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, MB R3E OV9, Canada.
Decker K; CancerCare Manitoba Research Institute, CancerCare Manitoba, Winnipeg, MB R3E OV9, Canada.; Epidemiology and Cancer Registry, CancerCare Manitoba, Winnipeg, MB R3E OV9, Canada.
Nachtigal MW; Obstetrics, Gynecology and Reproductive Sciences, University of Manitoba, Winnipeg, MB R3A 1R9, Canada.; CancerCare Manitoba Research Institute, CancerCare Manitoba, Winnipeg, MB R3E OV9, Canada.; Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, MB R3E OV9, Canada.
Altman AD; Obstetrics, Gynecology and Reproductive Sciences, University of Manitoba, Winnipeg, MB R3A 1R9, Canada.; CancerCare Manitoba Research Institute, CancerCare Manitoba, Winnipeg, MB R3E OV9, Canada.
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Źródło:
Current oncology (Toronto, Ont.) [Curr Oncol] 2022 Nov 30; Vol. 29 (12), pp. 9365-9376. Date of Electronic Publication: 2022 Nov 30.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Counseling*
Ovarian Neoplasms*/epidemiology
Ovarian Neoplasms*/genetics
Ovarian Neoplasms*/pathology
Humans ; Female ; Genes, BRCA1 ; Cohort Studies ; Genes, BRCA2 ; Manitoba/epidemiology ; Referral and Consultation
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Uptake of genetic counseling and testing in a clinic-based population of women with breast cancer.
Autorzy:
Wehbe A; Wayne State University School of Medicine, Detroit, Michigan, USA.
Manning M; Population Studies and Disparities Research Program, Barbara Ann Karmanos Cancer Institute, Detroit, Michigan, USA.; Department of Psychology, Oakland University, Rochester Hills, Michigan, USA.
Assad H; Population Studies and Disparities Research Program, Barbara Ann Karmanos Cancer Institute, Detroit, Michigan, USA.; Department of Oncology, Barbara Ann Karmanos Cancer Institute, Detroit, Michigan, USA.
Purrington KS; Population Studies and Disparities Research Program, Barbara Ann Karmanos Cancer Institute, Detroit, Michigan, USA.; Department of Oncology, Barbara Ann Karmanos Cancer Institute, Detroit, Michigan, USA.
Simon MS; Population Studies and Disparities Research Program, Barbara Ann Karmanos Cancer Institute, Detroit, Michigan, USA.; Department of Oncology, Barbara Ann Karmanos Cancer Institute, Detroit, Michigan, USA.
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Źródło:
Cancer medicine [Cancer Med] 2022 Sep; Vol. 11 (17), pp. 3304-3311. Date of Electronic Publication: 2022 Mar 23.
Typ publikacji:
Journal Article
MeSH Terms:
Breast Neoplasms*/diagnosis
Breast Neoplasms*/genetics
Breast Neoplasms*/therapy
Genetic Counseling*
Aged ; Female ; Genetic Testing ; Humans ; Medicare ; Referral and Consultation ; United States
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Reasons for failure of noninvasive prenatal test for cell-free fetal DNA in maternal peripheral blood.
Autorzy:
Kong X; Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver Disease, Peking University Hepatology Institute, Peking University People's Hospital, Beijing, China.
Zhang L; Prenatal Diagnosis Center, Peking University people's Hospital, Beijing, China.
Yang R; Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver Disease, Peking University Hepatology Institute, Peking University People's Hospital, Beijing, China.
Zhang H; Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver Disease, Peking University Hepatology Institute, Peking University People's Hospital, Beijing, China.
Ren M; Prenatal Diagnosis Center, Peking University people's Hospital, Beijing, China.
Wang X; Academic Support Department, Berry Genomics Corporation, Beijing, China.
Zhu L; Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver Disease, Peking University Hepatology Institute, Peking University People's Hospital, Beijing, China.
Chen H; Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver Disease, Peking University Hepatology Institute, Peking University People's Hospital, Beijing, China.
Rao H; Beijing Key Laboratory of Hepatitis C and Immunotherapy for Liver Disease, Peking University Hepatology Institute, Peking University People's Hospital, Beijing, China.
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Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Jan; Vol. 12 (1), pp. e2351.
Typ publikacji:
Journal Article
MeSH Terms:
Prenatal Diagnosis*
Prenatal Care*
Pregnancy ; Female ; Humans ; Genetic Counseling ; Fetus ; DNA/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Clinical application of targeted long read sequencing in prenatal beta-thalassemia testing and genetic counseling.
Autorzy:
Chin HL; Division of Genetics and Metabolism, Department of Paediatrics, Khoo Teck Puat-National University Children's Medical Institute, National University Hospital, Singapore, Singapore.; Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Benton MC; Oxford Nanopore Technologies, Singapore, Singapore.
Yang L; Oxford Nanopore Technologies, Singapore, Singapore.
Poon KS; Department of Laboratory Medicine, National University Hospital, Singapore, Singapore.
Tan KML; Department of Laboratory Medicine, National University Hospital, Singapore, Singapore.
Jamuar SS; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital, Singapore, Singapore.
Foo R; Cardiovascular Research Institute, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Law HY; DNA Diagnostic and Research Laboratory, KK Women's and Children's Hospital, Singapore, Singapore.
Goh DL; Division of Genetics and Metabolism, Department of Paediatrics, Khoo Teck Puat-National University Children's Medical Institute, National University Hospital, Singapore, Singapore.; Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Chong SS; Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.; Department of Laboratory Medicine, National University Hospital, Singapore, Singapore.; Department of Obstetrics and Gynaecology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
de Sessions PF; Oxford Nanopore Technologies, Singapore, Singapore.
Pokaż więcej
Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Jan; Vol. 12 (1), pp. e2285. Date of Electronic Publication: 2023 Sep 23.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
beta-Thalassemia*/diagnosis
beta-Thalassemia*/genetics
alpha-Thalassemia*/genetics
Humans ; Pregnancy ; Female ; Genetic Counseling ; Mutation ; Heterozygote
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The genetic counseling in a patient affected by choroideremia solved with the whole-exome sequencing approach.
Autorzy:
Sahin B; Department of Ophthalmology, Karaman State Hospital, Karaman, Turkey.
Burton E; Department of Neurology, LSU Health Shreveport, Shreveport, LA, USA.
Kuybu O; Department of Neurology, LSU Health Shreveport, Shreveport, LA, USA.
Sahin Y; Genoks Genetic Diseases Diagnostic Center, Ankara, Turkey.
Brinkley J; Department of Ophthalmology, LSU Health Shreveport, Shreveport, LA, USA.
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Źródło:
Indian journal of ophthalmology [Indian J Ophthalmol] 2022 Jul; Vol. 70 (7), pp. 2693-2694.
Typ publikacji:
Journal Article
MeSH Terms:
Choroideremia*/diagnosis
Choroideremia*/genetics
Genetic Counseling*
Humans ; Pedigree ; Sequence Analysis, DNA ; Exome Sequencing
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Pilot study of a culturally sensitive intervention to promote genetic counseling for breast cancer risk.
Autorzy:
Henderson V; Fred Hutchinson Cancer Center, 1100 Fairview Ave. N, Seattle, WA, 98109, USA. .
Madrigal JM; University of Illinois Cancer Center, 818 S. Wolcott Ave MC 709 SRH, Chicago, IL, 60612, USA.
Kendall LC; University of Illinois Cancer Center, 818 S. Wolcott Ave MC 709 SRH, Chicago, IL, 60612, USA.
Parekh P; University of Illinois College of Medicine, 1801 W Taylor St, Chicago, IL, 60612, USA.
Newsome J; Foundation for the National Institutes of Health, 11400 Rockville Pike #600, North Bethesda, MD, 20852, USA.
Chukwudozie IB; University of Illinois Cancer Center, 818 S. Wolcott Ave MC 709 SRH, Chicago, IL, 60612, USA.
Comer-Hagans L; University of Texas at Austin, 1501 Red River Street, Austin, TX, 78712, USA.
Coffey V; Governors State University College of Health and Human Services, 1 University Parkway, University Park, IL, 60484, USA.
Grumbach G; Governors State University College of Health and Human Services, 1 University Parkway, University Park, IL, 60484, USA.
Spencer S; Governors State University College of Health and Human Services, 1 University Parkway, University Park, IL, 60484, USA.
Rodgers C; Governors State University College of Health and Human Services, 1 University Parkway, University Park, IL, 60484, USA.
Kaur R; University of Illinois at Chicago College of Applied Health Sciences, 1919 W Taylor St MC517, Chicago, IL, 60612, USA.
Balay L; University of Illinois Hospital and Health Sciences System, 1801 W Taylor St, Chicago, IL, 60612, USA.
Maga T; University of Illinois Hospital and Health Sciences System, 1801 W Taylor St, Chicago, IL, 60612, USA.
Ramamonjiarivelo Z; Texas State University, 601 University Drive, San Marcos, TX, 78666, USA.
Balthazar C; Governors State University College of Health and Human Services, 1 University Parkway, University Park, IL, 60484, USA.
Winn R; Virginia Commonwealth University Massey Cancer Center, 401 College St Box 980037, Richmond, Virginia, 23298, USA.
Watson K; National Institutes of Health, All of Us Research Program, 200 Independence Ave, SW, Washington, DC, 20201, USA.
Odoms-Young A; Cornell University College of Human Ecology, Martha Van Rensselaer Hall, Ithaca, NY, 14853, USA.
Hoskins KF; University of Illinois College of Medicine, University of Illinois Hospital and Health Sciences System, 1801 W Taylor St, Chicago, IL, 60612, USA.
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Źródło:
BMC health services research [BMC Health Serv Res] 2022 Jun 25; Vol. 22 (1), pp. 826. Date of Electronic Publication: 2022 Jun 25.
Typ publikacji:
Clinical Study; Journal Article
MeSH Terms:
Breast Neoplasms*/diagnosis
Breast Neoplasms*/genetics
Breast Neoplasms*/prevention & control
Genetic Counseling*/psychology
Female ; Genetic Testing ; Humans ; Pilot Projects ; Prospective Studies
SCR Disease Name:
Breast Cancer, Familial
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Psychosocial impact of proactive rapid genetic counseling following breast cancer diagnosis.
Autorzy:
Kritzik R; Department of Oncology, Georgetown Lombardi Comprehensive Cancer, Georgetown University, Washington, District of Columbia, USA.
Usoro E; Department of Biology, University of the District of Columbia, Washington, District of Columbia, USA.
Peshkin BN; Department of Oncology, Georgetown Lombardi Comprehensive Cancer, Georgetown University, Washington, District of Columbia, USA.
Isaacs C; Department of Oncology, Georgetown Lombardi Comprehensive Cancer, Georgetown University, Washington, District of Columbia, USA.
Valdimarsdottir HB; Department of Population Health Science and Policy, Center for Behavioral Oncology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Willey S; Breast Cancer Program, Schar Cancer Institute, INOVA Health System, Fairfax, Virginia, USA.
O'Neill S; Department of Oncology, Georgetown Lombardi Comprehensive Cancer, Georgetown University, Washington, District of Columbia, USA.
DeMarco T; Cancer Genetics Program, INOVA Health System, Fairfax, Virginia, USA.
Nusbaum R; Department of Pediatrics, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Jandorf L; Department of Population Health Science and Policy, Center for Behavioral Oncology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Kelleher S; Department of Psychiatry and Behavioral Sciences, Duke University School of Medicine, Durham, North Carolina, USA.
Schwartz MD; Department of Oncology, Georgetown Lombardi Comprehensive Cancer, Georgetown University, Washington, District of Columbia, USA.
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Źródło:
Psycho-oncology [Psychooncology] 2022 May; Vol. 31 (5), pp. 788-797. Date of Electronic Publication: 2021 Dec 18.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
MeSH Terms:
Breast Neoplasms*/diagnosis
Breast Neoplasms*/genetics
Breast Neoplasms*/surgery
Genetic Counseling*/psychology
Counseling ; Female ; Genetic Testing ; Humans ; Quality of Life ; Referral and Consultation
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Predictors of premarital screening and genetic counseling knowledge and attitude among deaf and hard hearing females in Tabuk, Saudi Arabia.
Autorzy:
Zaien SZ; Department of Special Education, College of Art & Education, Tabuk University, Tabuk, Saudi Arabia.
El-Houfey AA; Community Health Nursing, Faculty of Nursing, Assiut University, Assiut, Egypt.; Department of Nursing, Jizan University, Jizan, Saudi Arabia.
Alqahtani H; Department of Special Education, College of Art & Education, Tabuk University, Tabuk, Saudi Arabia.
El Sayed HAE; Department of Medical Science Assistance, Community College, Tabuk University, Tabuk, Saudi Arabia.; Department of Community Health Nursing, Faculty of Nursing, Benha University, Benha, Egypt.
Elgzar WT; Department of Obstetrics and Gynecologic Nursing, Damanhour University, Damanhour, Egypt.; Department of Maternity and Childhood Nursing, Nursing College, Najran University, Najran, Saudi Arabia.
Essa RM; Department of Obstetrics and Gynecologic Nursing, Damanhour University, Damanhour, Egypt.
Bayomy H; Department of Nutrition and Food Science, University of Tabuk, Tabuk, Saudi Arabia.; Department of Food Science and Technology, Damanhour University, Damanhour, Egypt.
Ibrahim HA; Department of Maternity and Childhood Nursing, Nursing College, Najran University, Najran, Saudi Arabia.; Department of Obstetrics and Woman Health Nursing, Benha University, Benha, Egypt.
Pokaż więcej
Źródło:
Journal of medicine and life [J Med Life] 2022 Mar; Vol. 15 (3), pp. 379-386.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Counseling*
Hearing Loss*
Attitude ; Female ; Health Knowledge, Attitudes, Practice ; Hearing ; Humans ; Saudi Arabia
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
[Application of genetic counseling and preventive surgery in hereditary breast-ovarian cancer syndrome based on a rare family].
Autorzy:
Liu SH; Department of Gynecologic Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Dong L; Department of Pathology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Li B; Department of Gynecologic Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Zhao D; Department of Gynecologic Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Ying JM; Department of Pathology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
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Źródło:
Zhonghua zhong liu za zhi [Chinese journal of oncology] [Zhonghua Zhong Liu Za Zhi] 2023 Sep 23; Vol. 45 (9), pp. 796-802.
Typ publikacji:
English Abstract; Journal Article
MeSH Terms:
Breast Neoplasms*/genetics
Breast Neoplasms*/prevention & control
Breast Neoplasms*/surgery
Ovarian Neoplasms*/genetics
Ovarian Neoplasms*/prevention & control
Ovarian Neoplasms*/surgery
Humans ; Female ; Middle Aged ; Adult ; Genetic Counseling ; Genetic Predisposition to Disease ; Mutation
SCR Disease Name:
Breast Cancer, Familial
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Breast/ovarian cancer genetic counseling: Do anxiety, depression, and health care-related fears influence cancer worry and risk perception?
Autorzy:
Caruso A; Psychology Unit, IRCCS 'Regina Elena' National Cancer Institute, Rome, Italy.
Maggi G; Psychology Unit, IRCCS 'Regina Elena' National Cancer Institute, Rome, Italy.
Vigna C; Psychology Unit, IRCCS 'Regina Elena' National Cancer Institute, Rome, Italy.
Savarese A; Department of Oncology, IRCCS 'Regina Elena' National Cancer Institute, Rome, Italy.
Gallo L; Psychology Unit, IRCCS 'Regina Elena' National Cancer Institute, Rome, Italy.
Guariglia L; Psychology Unit, IRCCS 'Regina Elena' National Cancer Institute, Rome, Italy.
Casu G; Department of Psychology, University of Bologna, Bologna, Italy.
Gremigni P; Department of Psychology, University of Bologna, Bologna, Italy.
Pokaż więcej
Źródło:
Cancer medicine [Cancer Med] 2023 Sep; Vol. 12 (18), pp. 19215-19224. Date of Electronic Publication: 2023 Sep 14.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Breast Neoplasms*/epidemiology
Breast Neoplasms*/genetics
Breast Neoplasms*/psychology
Ovarian Neoplasms*/epidemiology
Ovarian Neoplasms*/genetics
Female ; Humans ; Genetic Counseling ; Depression/epidemiology ; Depression/etiology ; Depression/psychology ; Anxiety/etiology ; Anxiety/psychology ; Fear ; Delivery of Health Care ; Perception ; Genetic Predisposition to Disease
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Alfabetización genética en cuidadores frente a un asesoramiento genético pediátrico, en un hospital público de Buenos Aires.
Autorzy:
Vázquez, Natalia
Ortega, Javiera
Arberas, Claudia
Samaniego, Virginia C.
Skavone, Kevin
Assalone, Florencia
Vázquez, Victoria
Ruiz, Camila A.
Pozo Gowland, Rafael
Amayra Caro, Imanol
Pokaż więcej
Alternatywny tytuł:
Genetic literacy on caregivers who participate on pediatrics genetic counseling in a public hospital of Buenos Aires.
Źródło:
Interdisciplinaria: Revista de Psicología y Ciencias Afines. sep-dic2023, Vol. 40 Issue 3, p1-24. 24p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Genetic analysis and outcomes of Omani children with steroid‐resistant nephrotic syndrome.
Autorzy:
Al Riyami, Mohamed S. (AUTHOR)
Al Alawi, Intisar (AUTHOR)
Al Gaithi, Badria (AUTHOR)
Al Maskari, Anisa (AUTHOR)
Al Kalbani, Naifain (AUTHOR)
Al Hashmi, Nadia (AUTHOR)
Al Balushi, Aisha (AUTHOR)
Al Shahi, Maryam (AUTHOR)
Al Saidi, Suliman (AUTHOR)
Al Bimani, Muna (AUTHOR)
Al Hatali, Fahad (AUTHOR)
Mabillard, Holly (AUTHOR)
Sayer, John A. (AUTHOR)
Pokaż więcej
Źródło:
Molecular Genetics & Genomic Medicine. Sep2023, Vol. 11 Issue 9, p1-16. 16p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Report on the Effect of the Implementation of an Early Detection and Prevention of Cancer Program on Families at High Hereditary Risk—Concentrating on Patients Undergoing Genetic Diagnostics and Counseling in Central Poland.
Autorzy:
Kałużewski, Tadeusz (AUTHOR)
Kubiak, Izabela (AUTHOR)
Bednarek, Michał (AUTHOR)
Sałamunia, Jordan (AUTHOR)
Kucharska, Dorota (AUTHOR)
Kępczyński, Łukasz (AUTHOR)
Stempień, Marek (AUTHOR)
Kubicki, Tobiasz (AUTHOR)
Trzciński, Radzisław (AUTHOR)
Gordon-Sönmez, Zofia (AUTHOR)
Bartosińska-Dyc, Anna (AUTHOR)
Gach, Agnieszka (AUTHOR)
Kałużewski, Bogdan (AUTHOR)
Pokaż więcej
Źródło:
International Journal of Molecular Sciences. Sep2023, Vol. 24 Issue 17, p13178. 10p.
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 21-40 z 14288

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