Results 151 to 160 of about 15,648 (219)

A Rare Diagnosis of HPV-Positive Rectal Squamous Cell Carcinoma in a 59-Year-Old Heterosexual Woman: Implications for Screening Guidelines. [PDF]

Am J Case Rep
Adetiloye AO, Asif A, Badero OJ, Tan Z, Scott E.   +4 more
europepmc   +1 more source

Blurring the Lines: Co-Occurrence of MSH6 Variant and MLH1 Constitutional Epimutation in a Young Colorectal Cancer Patient. [PDF]

Clin Genet
Shtaya AA, Hadid Y, Mahamid A, Kidron D, Halpern N, Shalata A, Levi Z, Goldberg Y.   +7 more
europepmc   +1 more source

Cancro gástrico em síndrome de lynch num país de risco intermédio [PDF]

, 2015
Liliana Cristina Flores da Silva
core  

A Comprehensive Evaluation of Lymph Node Staging and a Proposal to Subdivide N2b Category in Colorectal Cancer Patients. [PDF]

Cancers (Basel)
Xi K, Wu Y, Feng L, Zhu Y, Fang H, Zhang H.   +5 more
europepmc   +1 more source

Genetic tumor syndromes in female cancer: insights into inherited cancer predisposition and clinical implications. [PDF]

Arch Gynecol Obstet
Krückel A, Gocke J, Hörner M, Keller K, Müller C, Brückner L, Heindl F, Hack CC, Beckmann MW, Amann N.   +9 more
europepmc   +1 more source

Rectal cancer in patients with hereditary nonpolyposis colorectal cancer: Surgical management and survival outcomes

Hereditary Cancer in Clinical Practice, 2011
Nancy You Y, Saraiya Devki S, Vu Thuy M, Veerapong Jula, Lynch Patrick M, Rodriguez-Bigas Miguel A   +5 more
doaj   +1 more source

An in-frame deletion mutation in MLH1 drives Lynch syndrome-associated colorectal cancer. [PDF]

BMC Cancer
Lin X, Bian C, Liang D, Li L, Tang Q, Li Q.   +5 more
europepmc   +1 more source

A missed opportunity for preventing CMMRD: is it time to include Lynch syndrome genes in prenatal genetic testing? [PDF]

BMJ Case Rep
Nair G, Cadenas N, Singh A.
europepmc   +1 more source

Artificial intelligence powered radiomics model for the assessment of colorectal tumor immune microenvironment. [PDF]

World J Gastrointest Oncol
Kumar S.
europepmc   +1 more source

Mono-allelic MUTYH mutation as the likely inherited etiology of hereditary breast cancer in a patient from a multi-cancer family- report of a family and literature review. [PDF]

BMC Med Genomics
Sarmadi A, Javanmard SH, Zeinalian M, Hosseinzadeh M, Tabatabaiefar MA.   +4 more
europepmc   +1 more source