Results 171 to 180 of about 34,649 (263)

Metachronous triple primary malignancies of duodenum, skin, and appendix in the absence of common hereditary syndromes: a case report. [PDF]

Am J Cancer Res
Qian DM, Zhou CH, Huang YH, Fan MH, Chen J.   +4 more
europepmc   +1 more source

Assessment of cancer risks due to ionizing radiations [PDF]

, 1987
Bannasch, Peter, Kellerer, Albrecht M.
core   +1 more source

Mycosis fungoides and Sézary syndrome

British Journal of Haematology, EarlyView.
Summary Mycosis fungoides (MF) and Sézary syndrome (SS) are the most common cutaneous T‐cell lymphomas, arising from mature CD4+ memory T cells. Diagnosis is complex and relies on clinicopathological correlation, immunophenotyping and molecular clonality testing, while management is stage‐adapted, with potentially curative outcomes achievable only in ...
Francisco Martins, Joana Calvão
wiley   +1 more source

Economic Evaluation of GARDE: A Digital Health Platform for Population-Level Hereditary Cancer Risk Assessment. [PDF]

JCO Oncol Pract
Ahsan MD, Kaphingst KA, Kohlmann WK, Bradshaw RL, Allen CG, Schlechter C, Kukhareva P, Maxwell W, Martin C, Davis-Rivera L, Madeo AC, Borsato EP, Frey MK, Kawamoto K, Fiol GD, Elkin EB, Sharaf RN.   +16 more
europepmc   +1 more source

Somatic and germline genetic testing pathways in haematological malignancies: Best practice consensus guidelines from the 2025 national meeting organised by UK Cancer Genetics Group (UKCGG), CanGene‐CanVar and the NHS England Haematological Oncology Working Group

British Journal of Haematology, EarlyView.
Summary Genomic technologies including next‐generation sequencing (NGS) and arrays for cytogenetic anomalies are now standard of care in England for the diagnostic evaluation of patients with suspected haematological malignancies. Challenges remain in the management of potential germline findings as a result of NGS panels and copy number variant ...
B. Speight, A. Hamblin, P. Talley, O. Tsoulaki, R. Robinson, P. Dean, J. Khorashad, A. Kulasekararaj, A. L. Godfrey, A. J. Mead, T. P. McVeigh, K. Snape, on behalf of Consensus Meeting Attendees   +12 more
wiley   +1 more source

Hereditary ovarian cancer. [PDF]

Discov Oncol
Jurgiel WA, Panasiuk B, Posmyk R.
europepmc   +1 more source

Familial Mediterranean Fever: A Diagnostic and Therapeutic Challenge. [PDF]

Cureus
Sia R.
europepmc   +1 more source

Malignant craniopharyngiomas: Institutional experience and literature review

Brain Pathology, EarlyView.
We report the second case of malignant craniopharyngioma with BAP1 and TP53 mutations. A literature review identified 44 cases of malignant craniopharyngiomas with a median overall survival of 6 months. Eighteen (41%) occurred in patients without any history of radiation, suggesting that mechanisms other than radiation have contributed to their ...
Thomas J. Auen, Isabella W. Zhang, Weiwei Zhang, Jordan M. Burr, Matthew L. Carda, James L. Wisecarver, Nicole Shonka, Jesse L. Cox, Sahara J. Cathcart, Allison Cushman‐Vokoun, Jie Chen   +10 more
wiley   +1 more source

Subsequent primary cancer risks for non-hereditary colorectal cancer survivors. [PDF]

EClinicalMedicine
Aung YK, Jenkins MA, Baxter NN, Potter JD, Schmit SL, Samadder JJ, Newcomb PA, Buchanan DD, Win AK.   +8 more
europepmc   +1 more source

Germline, hematopoietic, mosaic, and somatic variation: interplay between inherited and acquired genetic alterations in disease assessment [PDF]

, 2016

core   +1 more source