Gastrointestinal stromal tumors in the setting of multiple tumor syndromes-Reference-Cited by-同舟云学术

Gastrointestinal stromal tumors in the setting of multiple tumor syndromes

Published:2014-07 Issue:4 Volume:26 Page:408-414
ISSN:1040-8746
Container-title:Current Opinion in Oncology
language:en
Short-container-title:

Author:

Burgoyne Adam M.,Somaiah Neeta,Sicklick Jason K.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cancer Research,Oncology

Reference68 articles.

1. Hereditary and nonhereditary syndromic gastointestinal stromal tumours.;Agaimy;Pathologe,2010

2. A novel germline KIT mutation (p.L576P) in a family presenting with juvenile onset of multiple gastrointestinal stromal tumors, skin hyperpigmentations, and esophageal stenosis.;Neuhann;Am J Surg Pathol,2013

3. Familial gastrointestinal stromal tumor with germ line mutation of the juxtamembrane domain of the KIT gene observed in relatively young women.;Kuroda;Ann Diagn Pathol,2011

4. Gastrointestinal stromal tumor and other primary metachronous or synchronous neoplasms as a suspicion criterion for syndromic setting.;Ponti;Oncol Rep,2010

5. The triad of paragangliomas, gastric stromal tumours and pulmonary chondromas (Carney triad), and the dyad of paragangliomas and gastric stromal sarcomas (Carney-Stratakis syndrome): molecular genetics and clinical implications.;Stratakis;J Intern Med,2009

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