Results 101 to 110 of about 1,020 (131)

Genetics, genomics and clinical features of adenomatous polyposis. [PDF]

Fam Cancer
Joo JE, Viana-Errasti J, Buchanan DD, Valle L.   +3 more
europepmc   +1 more source

Immune checkpoint inhibitors in children with replication-repair-deficient high-grade gliomas. The South London Paediatric & TYA Neuro-Oncology Network experience

Perez-Somarriba M, Campello A, Benjamin P, Reisz Z, Bodi I, Al-Sarraj S, Bridges LR, Kumar A, Jacques TS, Zebian B, Bleil C, Aquilina K, Hettige S, Mastronuzzi A, Srivatsa K, Cockle J, Mandeville H, Marshall LV, Vaidya S, Stengs L, Bianchi V, Jones C, Lassaletta A, Das A, Tabori U, Carceller F.   +25 more
europepmc   +1 more source

Primary and metastatic brain tumours in hereditary cancer syndromes: case reports with and literature review. [PDF]

Hered Cancer Clin Pract
Robaczyńska J, Kiljańczyk M, Stachowski A, Lubiński K, Dodopoulos A, Benali R, Kiljańczyk A, Becht R, Cybulski C, Gronwald J, Lubiński J.   +10 more
europepmc   +1 more source

WITHDRAWN: Heterozygous germline MSH3 mutations, and probably MLH3 mutations, act as classical tumour suppressors, leading to excess somatic deletion mutations, signature ID4 and increased colorectal cancer risk

Soriano I, Sherwood K, Ward JC, Fernandez-Tajes J, Aman A, Thorn S, Gul G, Wilson J, Isaksson A, Glimelius B, Sjoblom T, Palles C, Tomlinson I.   +12 more
europepmc   +1 more source

Clinical Insights and Potential Benefits of Stem Cell Transplantation for Constitutional Mismatch Repair Deficiency: A Case Report of Two Siblings. [PDF]

Cureus
Mandryk M, Owoc-Lempach J, Cecot J, Zarzecki K, Piasta M, Wolska-Kolmus M, Marschollek P, Mielcarek-Siedziuk M, Dembowska-Bagińska B, Kałwak K.   +9 more
europepmc   +1 more source

Revisiting pediatric HGGs and PNETs according to the WHO CNS5 criteria: A clinical and genomic retrospective analysis. [PDF]

Neurooncol Adv
Kim JW, Choi SA, Lee S, Yun H, Phi JH, Park SH, Kim SK.   +6 more
europepmc   +1 more source

MSH2, MSH6, MLH1, and PMS2 immunohistochemistry as highly sensitive screening method for DNA mismatch repair deficiency syndromes in pediatric high-grade glioma. [PDF]

Acta Neuropathol
Friker LL, Perwein T, Waha A, Dörner E, Klein R, Blattner-Johnson M, Layer JP, Sturm D, Nussbaumer G, Kwiecien R, Spier I, Aretz S, Kerl K, Hennewig U, Rohde M, Karow A, Bluemcke I, Schmitz AK, Reinhard H, Hernáiz Driever P, Wendt S, Weiser A, Guerreiro Stücklin AS, Gerber NU, von Bueren AO, Khurana C, Jorch N, Wiese M, Kratz CP, Eyrich M, Karremann M, Herrlinger U, Hölzel M, Jones DTW, Hoffmann M, Pietsch T, Gielen GH, Kramm CM.   +37 more
europepmc   +1 more source

Insights into germline predisposition to pediatric lymphoid malignancies. [PDF]

Leukemia
Thapa R, Nichols KE, Sharma R.
europepmc   +1 more source

Clinical Impact of Germline Multigene Sequencing in Pediatric Cohorts with a Wide Spectrum of Neoplasms. [PDF]

Int J Mol Sci
Semenova V, Zhukovskaya E, Zelenova E, Kozlova V, Krasnov G, Levashov A, Sagoyan G, Belysheva T, Kharchikov D, Suleymanova A, Ivanova N, Lozovaya A, Rubanskaya M, Gelfer S, Sharapova E, Mikhaylova S, Valiev T, Karelin A, Varfolomeeva S, Nasedkina T.   +19 more
europepmc   +1 more source

Lynch Syndrome in Focus: A Multidisciplinary Review of Cancer Risk, Clinical Management, and Special Populations. [PDF]

Cancers (Basel)
Eroglu S, Birsenogul I, Bowen AP, Doyle JF, Pupkin SE, Villar J, Tarney CM, Gandia E, Pastor DM, Estrada-Veras JI.   +9 more
europepmc   +1 more source