Pediatric chordoma associated with tuberous sclerosis complex: A rare case report with a thorough analysis of potential therapeutic molecular targets-Reference-Cited by-同舟云学术

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Pediatric chordoma associated with tuberous sclerosis complex: A rare case report with a thorough analysis of potential therapeutic molecular targets

Published:2022-08 Issue:8 Volume:8 Page:e10291
ISSN:2405-8440
Container-title:Heliyon
language:en
Short-container-title:Heliyon

Author:

Anoshkin Kirill^ORCID,Zosen Denis^ORCID,Karandasheva Kristina,Untesco Maxim,Volodin Ilya,Alekseeva Ekaterina,Parfenenkova Anna,Snegova Eugenia,Kim Aleksandr,Dorofeeva Marina,Kutsev Sergei,Strelnikov Vladimir

Funder

Ministry of Education and Science of the Russian Federation

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference48 articles.

1. A review with emphasis on their pathophysiology, pathology, molecular biology, and genetics;Karpathiou;Pathol. Res. Pract.,2020

2. Chordoma;Ulici;Arch. Pathol. Lab. Med.,2022

3. Chordoma occurs in young children with tuberous sclerosis;Dahl;J. Neuropathol. Exp. Neurol.,2017

4. Whole genome sequencing of skull-base chordoma reveals genomic alterations associated with recurrence and chordoma-specific survival;Bai;Nat. Commun.,2021

5. Molecular targeted therapy in the treatment of chordoma: A systematic review;Meng;Front. Oncol.,2019

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