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Open access

Review article

First published 2025

Paving the way toward treatment solutions for CTNNB1 syndrome: a patient organization perspective

Špela Miroševič, Shivang Khandelwal, Emily Amerson [...]

Therapeutic Advances in Rare Disease

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Research article

First published 2003-7

Beckwith-Wiedemann Syndrome-associated Hepatoblastoma: Wnt Signal Activation Occurs Later in Tumorigenesis in Patients with 11p15.5 Uniparental Disomy

Ryuji Fukuzawa, Jun-ichi Hata, Yutaka Hayashi [...]

Pediatric and Developmental Pathology

Open access

Case report

First published 2018-4-13

When Rett syndrome is due to genes other than MECP2

Alan K. Percy, Jane Lane, Fran Annese [...]

Translational Science of Rare Diseases

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Case report

First published 2014-07

Familial Adenomatous Polyposis–Associated,Cribriform Morular Variant of Papillary Thyroid Carcinoma Harboring a K-RAS Mutation: Case Presentation and Review of Molecular Mechanisms

Silvana M. Giannelli, Laron McPhaul, Jon Nakamoto [...]

Thyroid®

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Case report

First published 2010-5

Cushing's Syndrome in an Infant Secondary to Malignant Adrenocortical Tumors with Somatic Mutation of Beta-Catenin

Theerawut Pusantisampan, Surasak Sangkhathat, Kanita Kayasut [...]

Pediatric and Developmental Pathology

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Case report

First published 2021-1

Adipocyte-rich CTNNB1 -mutated Intramuscular Gardner Fibroma Progressing to Desmoid Fibromatosis

Andrea Bakker, Jonathan C Slack, Mara Caragea [...]

Pediatric and Developmental Pathology

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Case report

First published 2022-11

Hepatocellular Adenoma in an Infant With Burn-McKeown Syndrome: Report of a Case

Iván A. González, Lea F. Surrey, Pierre Russo

Pediatric and Developmental Pathology

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Case report

First published 2019-5

Cribriform-Morular Variant of Papillary Thyroid Carcinoma With Poorly Differentiated Features: A Case Report With Immunohistochemical and Molecular Genetic Analysis

Jessica Corean, Larissa V. Furtado, Sabah Kadri [...]

International Journal of Surgical Pathology

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