| PubMed |
Abstract |
RScore(About this table) |
| 19738042 |
Brems H, Park C, Maertens O, Pemov A, Messiaen L, Upadhyaya M, Claes K, Beert E, Peeters K, Mautner V, Sloan JL, Yao L, Lee CC, Sciot R, De Smet L, Legius E, Stewart DR: Glomus tumors in neurofibromatosis type 1: genetic, functional, and clinical evidence of a novel association. Cancer Res. 2009 Sep 15;69(18):7393-401. Epub 2009 Sep 8.
Neurofibromatosis type 1 (NF1) is a common disorder that arises secondary to mutations in the tumor suppressor gene NF1. |
10(0,0,0,10) |
Details |
| 17696922 |
Ausmus GG, Piliang MP, Bergfeld WF, Goldblum JR: Soft-tissue perineurioma in a 20-year-old patient with neurofibromatosis type 1 (NF1): report of a case and review of the literature. J Cutan Pathol. 2007 Sep;34(9):726-30.
|
3(0,0,0,3) |
Details |
| 19833474 |
Mendonca CT, Weingartner J, de Carvalho CA, Costa DS: Endovascular treatment of contained rupture of a superior mesenteric artery aneurysm resulting from neurofibromatosis type I. J Vasc Surg. 2010 Feb;51(2):461-4. Epub 2009 Oct 14.
|
2(0,0,0,2) |
Details |
| 19319643 |
Dell'Avanzato R, Carboni F, Palmieri MB, Palmirotta R, Guadagni F, Pippa G, Santeusanio G, Antimi M, Lopez M, Carlini M: Laparoscopic resection of sporadic synchronous gastric and jejunal gastrointestinal stromal tumors: report of a case. Surg Today. 2009;39(4):335-9. Epub 2009 Mar 25.
Multicentricity of gastrointestinal stromal tumors (GISTs) has been described only in patients with neurofibromatosis type 1 (NF1) or within the small intestine, and different pathogenetic mechanisms are involved. |
1(0,0,0,1) |
Details |