| dc.contributor.author | Gork, S | |
| dc.contributor.author | Ariturk, E | |
| dc.contributor.author | Baris, S | |
| dc.contributor.author | Ariturk, N | |
| dc.contributor.author | Bernay, F | |
| dc.contributor.author | Rizalar, R | |
| dc.contributor.author | Gurses, N | |
| dc.date.accessioned | 2020-06-21T15:53:43Z | |
| dc.date.available | 2020-06-21T15:53:43Z | |
| dc.date.issued | 1996 | |
| dc.identifier.issn | 0179-0358 | |
| dc.identifier.uri | https://doi.org/10.1007/BF00497839 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/22731 | |
| dc.description | WOS: A1996UX90000046 | en_US |
| dc.description | PubMed: 24057742 | en_US |
| dc.description.abstract | Juvenile xanthogranuloma (JX) is a regressing fibrous histiocytoma occurring during infancy and characterized by cutaneous papules and nodules and less often by additional lesions in deep tissue and organs. It has a special place among childhood masses by presenting differ ent outcomes and spontaneous regression. We report three cases of JX that were detected after birth and resected. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Springer Verlag | en_US |
| dc.relation.isversionof | 10.1007/BF00497839 | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | juvenile xanthogranuloma | en_US |
| dc.title | Juvenile xanthogranuloma: Three cases | en_US |
| dc.type | article | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 11 | en_US |
| dc.identifier.issue | 05.Jun | en_US |
| dc.identifier.startpage | 427 | en_US |
| dc.identifier.endpage | 428 | en_US |
| dc.relation.journal | Pediatric Surgery International | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
