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Open access

Case report

First published 2020-6

Successful treatment of a patient with NSCLC carrying uncommon compound EGFR G719X and S768I mutations using osimertinib: A case report

Yangyang Cai, Yizhuo Wang, Jingnan Sun [...]

Journal of International Medical Research

Open access

Research article

First published 2025-09

Real-World Evidence for First-Line afatinib in Advanced Non-Small Cell Lung Cancer With Uncommon Epidermal Growth Factor Receptor Mutations Other than G719X/L861Q/S768I

Thanh Ha Vu, Hoa Thai Thi Nguyen, To Van Ta [...]

Cancer Control

Open access

Research article

First published 2024

Real-world analysis of afatinib as a first-line treatment for patients with advanced stage non-small-cell lung cancer with uncommon EGFR mutations: a multicenter study in Vietnam

Van Luan Pham, Tuan Anh Le, Cam Phuong Pham [...]

Therapeutic Advances in Medical Oncology

Retricted access

Case report

First published 2010-9

Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome Associated with p 63 Mutation and an Uncommon Phenotype

Lívia Máris Ribeiro Paranaíba, Hercílio Martelli-Júnior, Roseli Teixeira De Miranda [...]

The Cleft Palate Craniofacial Journal

Open access

Research article

First published 2025

Excellent survival benefit achieved in patients with advanced-stage non-small cell lung cancer harboring the epidermal growth factor receptor-G719X mutation treated by afatinib: the real-world data from a multicenter study in Vietnam

Van Luan Pham, Cam Phuong Pham, Thi Thai Hoa Nguyen [...]

Therapeutic Advances in Respiratory Disease

Retricted access

Research article

First published 2000-06

Uncommon Mutations and Polymorphisms in the Hemochromatosis Gene

Jennifer J. Pointon, Daniel Wallace, Alison T. Merryweather-Clarke [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Case report

First published 2017-11

Uncommon Somatic Mutations in Metastatic NUT Midline Carcinoma

Stefano Cavalieri, Anastasios Stathis, Alessandra Fabbri [...]

Tumori Journal

Retricted access

Research article

First published 2016-02

Uncommon TERT Promoter Mutations in Pediatric Thyroid Cancer

Ali S. Alzahrani, Ebtesam Qasem, Avaniyapuram Kannan Murugan [...]

Thyroid®

Retricted access

Research article

First published 2011-4

Bilateral Polymicrogyria and MELAS/A3243G Mutation. A Very Uncommon Association

A. Vidal, M. Castillo

The Neuroradiology Journal

Retricted access

Research article

First published 2005-04

BRAF Mutations are Uncommon in Papillary Thyroid Cancer of Young Patients

Karen Penko, Jeffrey Livezey, Cydney Fenton [...]

Thyroid®

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