NF1-Associated Gastrointestinal Stromal Tumors Have Unique Clinical, Phenotypic, and Genotypic Characteristics-Reference-Cited by-同舟云学术

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NF1-Associated Gastrointestinal Stromal Tumors Have Unique Clinical, Phenotypic, and Genotypic Characteristics

Published:2005-09 Issue:9 Volume:29 Page:1170-1176
ISSN:0147-5185
Container-title:American Journal of Surgical Pathology
language:en
Short-container-title:

Author:

Andersson Johanna,Sihto Harri,Meis-Kindblom Jeanne M,Joensuu Heikki,Nupponen Nina,Kindblom Lars-Gunnar

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pathology and Forensic Medicine,Surgery,Anatomy

Reference48 articles.

1. The complexity of KIT gene mutations and chromosome rearrangements and their clinical correlation in gastrointestinal stromal (pacemaker cell) tumors.;Andersson;Am J Pathol,2002

2. Neurofibrosarcoma-derived Schwann cells overexpress platelet-derived growth factor (PDGF) receptors and are induced to proliferate by PDGF BB.;Badache;J Cell Physiol,1998

3. Expression of Kit in neurofibromin-deficient human Schwann cells: role in Schwann cell hyperplasia associated with type 1 neurofibromatosis.;Badache;Oncogene,1998

4. Separate occurrence of extra-adrenal paraganglioma and gastrointestinal stromal tumor in monozygotic twins: probable familial Carney syndrome.;Boccon-Gibod;Pediatr Dev Pathol,2004

5. Gastric stromal sarcoma, pulmonary chondroma, and extra-adrenal paraganglioma (Carney Triad): natural history, adrenocortical component, and possible familial occurrence.;Carney;Mayo Clin Proc,1999

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