4,644 results match your criteria: "Neoplastic Syndromes Hereditary"

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Clinical decision tree for optimizing endoscopic assessment of signet ring cell carcinoma in hereditary diffuse gastric cancer surveillance.
Lianlian Wu, Judith Honing, Anjui Wu, Sonia S Kupfer, Tanya M Bisseling

Endoscopy· October 2025

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Cancer statistics, 2023.
Rebecca L Siegel, Kimberly D Miller, Nikita Sandeep Wagle, Ahmedin Jemal

CA Cancer J Clin· January 2023

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Universal Germline Genetic Testing for Hereditary Cancer Syndromes in Patients With Solid Tumor Cancer.
Edward D Esplin, Sarah M Nielsen, Sara L Bristow, Judy E Garber, Heather Hampel

JCO Precis Oncol· September 2022

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Gastrointestinal: Massive gastric juvenile polyposis.
X Cheng, X Sun, Q Wang

December 2021

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Safety of cold snare polypectomy for duodenal adenomas in familial adenomatous polyposis: a prospective exploratory study.
Kenta Hamada, Yoji Takeuchi, Hideki Ishikawa, Yasumasa Ezoe, Masamichi Arao

Endoscopy· May 2018

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Functional assessment and treatment of perseverative speech about restricted topics in an adolescent with Asperger syndrome.
Wayne W Fisher, Nicole M Rodriguez, Todd M Owen

J Appl Behav Anal· May 2014

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Genotype-phenotype correlations in -associated tumour syndrome: case report and literature review.
Agata Bukowska, Henrik Horváth, Karl Heinimann

Swiss Med Wkly· December 2025

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Gynecologic Manifestations of Hereditary Syndromes: Clinical and Imaging Spectrum.
Ekta Maheshwari, Shaun A Wahab, Ashish P Wasnik, Katherine E Maturen, Phuong L Mai

Radiographics· January 2026

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Significant progress in hereditary gastrointestinal cancer research presented at the meeting of the International Society for Gastrointestinal Hereditary Tumors (InSiGHT) 10th meeting of InSiGHT, June 19th -22nd, 2024, Barcelona, Spain.
H F A Vasen

Fam Cancer· December 2025

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Advanced CYLD Cutaneous Syndrome (CCS) Treated With the Hedgehog Signaling Pathway Inhibitor Vismodegib Results in a Limited Clinical Response.
Jeanette Kaae, Lise Mette Rahbek Gjerdrum, Tim Svenstrup Poulsen, Estrid Hoegdall, Gregor Borut Jemec

APMIS· December 2025

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Immunotherapy for downstaging of locally advanced mismatch repair deficient colorectal cancer: A prospective institutional case series.
Maeve A O'Neill, Emily C Harrold, Charles Gillham, Ciara Ryan, Brian J Mehigan

Eur J Surg Oncol· January 2026

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[Metachronous colon cancer after successful treatment of mismatch repair-deficient metastatic colorectal cancer].
Line Hansen, Michael Bødker Lauritzen, Christian Thomsen, Inga Makieva, Malene Lundsgaard

Ugeskr Laeger· November 2025

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Tumor Predisposition Syndromes: An Imaging Review.
Carlos Robles, Suzanne Laughlin, Vivek Pai

Neuroimaging Clin N Am· February 2026

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Clinical challenges of cancer predisposition syndromes with pediatric central nervous system tumors: a single-center study.
Hirohito Kubota, Kohei Fukuoka, Yuki Arakawa, Yoshinori Uchihara, Junko Takita

Childs Nerv Syst· November 2025

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Parents' perspectives of non-informative germline genetic testing in children with Juvenile Polyposis Syndrome.
Kayla Rud, Kelcy Smith-Simmer, Jennifer Weiss, Kristina Garcia

J Genet Couns· December 2025

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Manipulation with Mutational Status of VHL Regulates Hypoxic Metabolism and Pro-Angiogenic Phenotypes in ccRCC Caki-1 Cells.
Pavel Abramov, Alexandr Mazur, Aleksey Starshin, Svetlana Zhenilo, Egor Prokhortchouk

Int J Mol Sci· October 2025

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A missed opportunity for preventing CMMRD: is it time to include Lynch syndrome genes in prenatal genetic testing?
Geethu Nair, Nicola Cadenas, Aparajita Singh

BMJ Case Rep· November 2025

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"The Nurse's Role in Genetic Counseling for Hereditary Neoplastic Syndromes: A Scoping Review".
Silvana Maria Barros de Oliveira, Paulyne Souza Silva Guimarães, Márcia Mirian Rosendo Aleluia, Alda Graciele Claudio Dos Santos Almeida, Patrícia de Carvalho Nagliate

Semin Oncol Nurs· October 2025

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Juvenile polyposis syndrome with germline SMAD4 mutation: case series in tertiary care and critical review of literature.
F Vulsteke, V D'Cruz, L Krott, S Moura Ribeiro, E Van Daele

Acta Gastroenterol Belg· October 2025

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Incidence of Mismatch Repair Deficiency in Rectal Cancer and Response to Neoadjuvant Treatment.
Jelle A Nieuwstraten, Eline G M van Geffen, Martijn W H Leenders, Pieter J Tanis, Miranda Kusters

Clin Colorectal Cancer· December 2025

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Cancer Predisposition Syndromes With Involvement of the Head and Neck Regions in Children: An Imaging Guide.
Livja Mertiri, Nilesh Desai, Maarten Lequin, Denada Mertiri, Hui Brandon Tran

J Neuroimaging· October 2025

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Non-truncating BMPR1A variants associated with familial colorectal cancer and adenomatous polyps.
Taina T Nieminen, Outi Kuismin, Riitta Laine, Anna Lepistö, Laura Koskenvuo

BMC Cancer· September 2025

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Hereditary Cancer Syndromes in Familial Breast Cancer: Insights Into Proactive Gastric Cancer Surveillance.
Jennifer Wiese, Swapna Sirigireddy, Abdelwahap Elghezewi, Ibrahim Shanti, Mikayla Myers

J Investig Med High Impact Case Rep· September 2025

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Cancer spectrum in Mexican patients with the CHEK2 p.(Leu236Pro) variant: a retrospective study.
L Leonardo Flores-Lagunes, Rosa María Alvarez-Gómez, Carolina Molina-Garay, Marco Jimenez-Olivares, Pablo Arturo Acosta-Mendez

Fam Cancer· September 2025

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How We Approach the Integration of Psychological Services in the Care of Children With Cancer Predisposition Syndromes.
Joan W Hanania, Rowan Forbes Shepherd, Lori Wiener, Katianne M Howard Sharp, Morgan N Similuk

Pediatr Blood Cancer· December 2025

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Quality of Life in Adult Individuals Living With or at Risk of a Hereditary Cancer Predisposition Syndrome: A Scoping Review of the Qualitative Literature.
M Sztankay, S Wheelwright, V Vassiliou, E M A Bleiker, B Rahman

Cancer Med· September 2025

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Implementing a Genetic Counselor-Led Model for Hereditary Myeloid Malignancies: A Real-World Study.
Madeline VanDerGraaf, Georgianne Younger, Kyle Dillahunt, Jennifer Smith, Athena Puski

Cancer Med· September 2025

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Metastasectomy outcomes in renal cell carcinoma: insights from hereditary leiomyomatosis and succinate dehydrogenase deficient cohorts.
Milan H Patel, Ruben Blachman-Braun, Braden Millan, Lauren Loebach, Jaskirat Saini

Urol Oncol· December 2025

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Quantifying evidence for phenotypic specificity (PP4) for syndromic phenotypes: Large-scale integration of rare germline FH variants from diagnostic laboratory testing for HLRCC and renal cancer.
Sophie Allen, Charlie F Rowlands, Samantha Butler, Miranda Durkie, Carrie Horton

Genet Med· November 2025

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Multiple early onset atypical cutaneous fibrous histiocytomas in multilocus inherited neoplasia allele syndrome involving and genes.
Schaida Schirwani, Sylvia Ghattas, Nicholas Wilson, Samantha Hunt, Alison Callaway

J Med Genet· November 2025

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Risk Assessment and Fertility Counseling for Hereditary Gynecological Cancer Syndromes.
Mei Zhao, Xiao-Ming Teng, Qiang Yan, Fan Hao

Cancer Med· September 2025

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Bilateral, multicystic fumarate hydratase-deficient renal cell carcinoma in patient with hereditary leiomyomatosis & renal cell carcinoma syndrome: A case report and review of the literature.
Ashlie E Rubrecht, Jennifer H Aldrink, Patrick Warren, Mariam T Mathew, Karen Tsuchiya

Diagn Pathol· August 2025

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Development of a functional assay for the characterisation of variants from the French haemorrhagic hereditary telangiectasia cohort.
Louane Despas, Lea Vialet, Maud Tusseau, Valentin Azemard, Lea Beurier-Soulat

J Med Genet· November 2025

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