An orbital Langerhan's histiocytosis case of the childhood

dc.contributor.buuauthorBekar, Ahmet
dc.contributor.buuauthorAksoy, Kasım
dc.contributor.buuauthorDoğan, Şeref
dc.contributor.buuauthorTolunay, Şahsene
dc.contributor.buuauthorSevinir, Betül
dc.contributor.buuauthorÖzmen, Ahmet
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Nöroşirurji Anabilim Dalı.tr_TR
dc.contributor.researcheridAAH-1570-2021tr_TR
dc.date.accessioned2021-09-16T12:51:39Z
dc.date.available2021-09-16T12:51:39Z
dc.date.issued1997
dc.descriptionBu çalışma, Amsterdam[Hollanda]'da 6-11 Temmuz 1997 tarihinde düzenlenen 11th International Congress of Neurological Surgery'de bildiri olarak sunulmuştur.tr_TR
dc.description.abstractLangerhan's cell histiocytosis (LCH) is characterised by the local and diffuse infiltration of monocytes which originated from the promonocytes of the bone marrow. Central nervous system involvement occurs in Hand-Schuller-Christian disease and Letterer-Siwe syndrome. LCH of the orbita is reported to be rare in childhood. A one-;year old boy who had pure bone involvement is presented here and the diagnostic and therapeutic approaches are discussed in the light of the literature.en_US
dc.identifier.citationBekar, A. vd. (1997). "An orbital Langerhan's histiocytosis case of the childhood". 11th International Congress of Neurological Surgery, 1-2, 2185-2189.en_US
dc.identifier.endpage2189tr_TR
dc.identifier.isbn88-323-0706-5
dc.identifier.startpage2185tr_TR
dc.identifier.urihttp://hdl.handle.net/11452/21998
dc.identifier.volume1-2tr_TR
dc.identifier.wosA1997BJ48C00376tr_TR
dc.indexed.wosCPCIStr_TR
dc.language.isoenen_US
dc.publisherMonduzzi Editoreen_US
dc.relation.journal11th International Congress of Neurological Surgeryen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararasıtr_TR
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectNeurosciences & neurologyen_US
dc.subject.wosClinical neurologyen_US
dc.titleAn orbital Langerhan's histiocytosis case of the childhooden_US
dc.typeArticle

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