Publication
Multiple glomus tumors and segmental neurofibromatosis: there are no coincidences
| dc.contributor.author | Cabral, R | |
| dc.contributor.author | Santiago, F | |
| dc.contributor.author | Tellechea, O | |
| dc.date.accessioned | 2011-11-08T16:09:29Z | |
| dc.date.available | 2011-11-08T16:09:29Z | |
| dc.date.issued | 2011 | |
| dc.description.abstract | Segmental neurofibromatosis is a rare subtype of neurofibromatosis type 1 (NF1). Glomus tumors are uncommon benign tumors. The authors report the association between these two rare conditions, not yet reported. | por |
| dc.identifier.citation | Dermatol Online J. 2011 Mar 15;17(3):4. | por |
| dc.identifier.uri | http://hdl.handle.net/10400.4/1119 | |
| dc.language.iso | eng | por |
| dc.peerreviewed | yes | por |
| dc.subject | Neoplasias Primárias Múltiplas | por |
| dc.subject | Tumor glómico | por |
| dc.subject | Neoplasias da Pele | por |
| dc.subject | Neurofibromatose 1 | por |
| dc.title | Multiple glomus tumors and segmental neurofibromatosis: there are no coincidences | por |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| rcaap.rights | openAccess | por |
| rcaap.type | article | por |
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