UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 673

Sortiert nach

Counseling about Cancer: Strategies for Genetic Counseling

Fourth edition, 2023

Volltextzugriff (PDF)

Cowden Syndrome and the PTEN Hamartoma Tumor Syndrome: Systematic Review and Revised Diagnostic Criteria

JNCI : Journal of the National Cancer Institute, 2013-11, Vol.105 (21), p.1607-1616

2013

Volltextzugriff (PDF)

A Rapid Systematic Review of Outcomes Studies in Genetic Counseling

Journal of genetic counseling, 2017-06, Vol.26 (3), p.361-378

2017

Volltextzugriff (PDF)

Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment

JAMA oncology, 2015-10, Vol.1 (7), p.943

2015

Volltextzugriff (PDF)

A tailored approach to BRAF and MLH1 methylation testing in a universal screening program for Lynch syndrome

Modern pathology, 2017-03, Vol.30 (3), p.440-447

2017

Volltextzugriff (PDF)

Mainstreamed genetic testing of breast cancer patients: experience from a single surgeon’s practice in a large US Academic Center

Familial cancer, 2023-10, Vol.22 (4), p.467-474

2023

Volltextzugriff (PDF)

Identification of 4‑(Aminomethyl)-6-(trifluoromethyl)-2-(phenoxy)pyridine Derivatives as Potent, Selective, and Orally Efficacious Inhibitors of the Copper-Dependent Amine Oxidase, Lysyl Oxidase-Like 2 (LOXL2)

Journal of medicinal chemistry, 2017-05, Vol.60 (10), p.4403-4423

2017

Volltextzugriff (PDF)

Transition to telephone genetic counseling services during the COVID‐19 pandemic

Journal of genetic counseling, 2021-08, Vol.30 (4), p.984-988

2021

Volltextzugriff (PDF)

Selective Inhibition of Autotaxin Is Efficacious in Mouse Models of Liver Fibrosis

The Journal of pharmacology and experimental therapeutics, 2017-01, Vol.360 (1), p.1

2017

Volltextzugriff (PDF)

Case 7-2020: A 52-Year-Old Man with a Mass in the Left Breast

The New England journal of medicine, 2020-02, Vol.382 (9), p.856-864

2020

Volltextzugriff (PDF)

ATM Variants in Breast Cancer: Implications for Breast Radiation Therapy Treatment Recommendations

International journal of radiation oncology, biology, physics, 2021-08, Vol.110 (5), p.1373-1382

2021

Volltextzugriff (PDF)

Development of an Electronic Decision Aid Tool to Facilitate Mainstream Genetic Testing in Ovarian Cancer Patients

The oncologist (Dayton, Ohio), 2024-05, Vol.29 (5), p.e665-e671

2024

Volltextzugriff (PDF)

Patient decisions regarding cancer gene panel testing: An exploratory study

Journal of genetic counseling, 2023-11

2023

Volltextzugriff (PDF)

Identification of Somatically Acquired BRCA1/2 Mutations by cfDNA Analysis in Patients with Metastatic Breast Cancer

Clinical cancer research, 2020-09, Vol.26 (18), p.4852-4862

2020

Volltextzugriff (PDF)

Performance of the shared decision-making process scale for use in evaluation of hereditary cancer genetic testing decisions

Journal of genetic counseling, 2023-10, Vol.32 (5), p.957-964

2023

Volltextzugriff (PDF)

Pathologic Findings in Prophylactic and Nonprophylactic Hysterectomy Specimens of Patients With Lynch Syndrome

The American journal of surgical pathology, 2016-09, Vol.40 (9), p.1177-1191

2016

Volltextzugriff (PDF)

Prevalence of Thyroid Cancer in Familial Adenomatous Polyposis Syndrome and the Role of Screening Ultrasound Examinations

Clinical gastroenterology and hepatology, 2007-03, Vol.5 (3), p.367-373

2007

Volltextzugriff (PDF)

Perceptions of Cancer Risk, Cause, and Needs in Participants from Low Socioeconomic Background at Risk for Hereditary Cancer

Behavioral medicine (Washington, D.C.), 2017-10, Vol.43 (4), p.259-267

2017

Volltextzugriff (PDF)

Prevalence and Predictors of Appropriate Colorectal Cancer Surveillance in Lynch Syndrome

The American journal of gastroenterology, 2010-08, Vol.105 (8), p.1851-1860

2010

Volltextzugriff (PDF)

Sharing Genetic Test Results in Lynch Syndrome: Communication With Close and Distant Relatives

Clinical gastroenterology and hepatology, 2008-03, Vol.6 (3), p.333-338

2008

Volltextzugriff (PDF)

Finding a Balance: Reconciling the Needs of the Institution, Patient, and Genetic Counselor for Optimal Resource Utilization

Journal of genetic counseling, 2018-12, Vol.27 (6), p.1318-1327

2018

Volltextzugriff (PDF)

Enhancing the Identification of Lynch Syndrome Through Universal Screening of Both Endometrial and Colon Cancers

Gastroenterology (New York, N.Y. 1943), 2017-04, Vol.152 (5), p.S178-S178

2017

Volltextzugriff (PDF)

Heterozygous Germ Line hCHK2 Mutations in Li-Fraumeni Syndrome

Science (American Association for the Advancement of Science), 1999-12, Vol.286 (5449), p.2528-2531

1999

Volltextzugriff (PDF)

Hereditary melanoma: Update on syndromes and management

Journal of the American Academy of Dermatology, 2016-03, Vol.74 (3), p.395-407

2016

Volltextzugriff (PDF)

1 – 25 von 673

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(613)
Mit Volltextzugriff
(592)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(673)
Japanisch
(44)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(8)

Menü

Weitere Dienste

Einstellungen

Counseling about Cancer: Strategies for Genetic Counseling

Cowden Syndrome and the PTEN Hamartoma Tumor Syndrome: Systematic Review and Revised Diagnostic Criteria

A Rapid Systematic Review of Outcomes Studies in Genetic Counseling

Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment

A tailored approach to BRAF and MLH1 methylation testing in a universal screening program for Lynch syndrome

Mainstreamed genetic testing of breast cancer patients: experience from a single surgeon’s practice in a large US Academic Center

Identification of 4‑(Aminomethyl)-6-(trifluoromethyl)-2-(phenoxy)pyridine Derivatives as Potent, Selective, and Orally Efficacious Inhibitors of the Copper-Dependent Amine Oxidase, Lysyl Oxidase-Like 2 (LOXL2)

Transition to telephone genetic counseling services during the COVID‐19 pandemic

Selective Inhibition of Autotaxin Is Efficacious in Mouse Models of Liver Fibrosis

Case 7-2020: A 52-Year-Old Man with a Mass in the Left Breast

ATM Variants in Breast Cancer: Implications for Breast Radiation Therapy Treatment Recommendations

Development of an Electronic Decision Aid Tool to Facilitate Mainstream Genetic Testing in Ovarian Cancer Patients

Patient decisions regarding cancer gene panel testing: An exploratory study

Identification of Somatically Acquired BRCA1/2 Mutations by cfDNA Analysis in Patients with Metastatic Breast Cancer

Performance of the shared decision-making process scale for use in evaluation of hereditary cancer genetic testing decisions

Pathologic Findings in Prophylactic and Nonprophylactic Hysterectomy Specimens of Patients With Lynch Syndrome

ATRAID regulates the action of nitrogen-containing bisphosphonates on bone

Prevalence of Thyroid Cancer in Familial Adenomatous Polyposis Syndrome and the Role of Screening Ultrasound Examinations

Perceptions of Cancer Risk, Cause, and Needs in Participants from Low Socioeconomic Background at Risk for Hereditary Cancer

Prevalence and Predictors of Appropriate Colorectal Cancer Surveillance in Lynch Syndrome

Sharing Genetic Test Results in Lynch Syndrome: Communication With Close and Distant Relatives

Finding a Balance: Reconciling the Needs of the Institution, Patient, and Genetic Counselor for Optimal Resource Utilization

Enhancing the Identification of Lynch Syndrome Through Universal Screening of Both Endometrial and Colon Cancers

Heterozygous Germ Line hCHK2 Mutations in Li-Fraumeni Syndrome

Hereditary melanoma: Update on syndromes and management

Suchergebnisse filtern