Cerebral Involvement of Hemophagocytic Lymphohistiocytosis in Griscelli Syndrome

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dc.contributor.authorToret, Ersin
dc.contributor.authorAy, Yılmaz
dc.contributor.authorAksoylar, Serap
dc.contributor.authorKarapınar, Tuba Hilkay
dc.contributor.authorOymak, Yeşim
dc.date.accessioned2020-12-01T12:37:25Z
dc.date.available2020-12-01T12:37:25Z
dc.date.issued2019
dc.departmentEge Üniversitesien_US
dc.description.abstractType II Griscelli Syndrome (GS) is caused by a mutation in the RAB27A gene and usually manifests with silvery-gray hair, immune deficiency and the development of hemophagocytic lymphohistiocytosis (HLH). A hematopoietic stem cell transplantation is the curative treatment for HLH and reduced-intensity conditioning prevents the morbidity/mortality in the transplantation related to myeloablative conditioning. We report on a 21-month old boy with cerebral involvement of HLH related to GS.en_US
dc.identifier.doi10.4274/jpr.galenos.2018.33254
dc.identifier.endpage255en_US
dc.identifier.issn2147-9445
dc.identifier.issn2587-2478
dc.identifier.issue3en_US
dc.identifier.startpage252en_US
dc.identifier.urihttps://doi.org/10.4274/jpr.galenos.2018.33254
dc.identifier.urihttps://app.trdizin.gov.tr//makale/TXpjNU5UQXdNQT09
dc.identifier.urihttps://hdl.handle.net/11454/67174
dc.identifier.volume6en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofThe Journal of Pediatric Researchen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subject0-Belirleneceken_US
dc.titleCerebral Involvement of Hemophagocytic Lymphohistiocytosis in Griscelli Syndromeen_US
dc.typeArticleen_US

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