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dc.contributor.authorSaribeyoglu, ET
dc.contributor.authorAnak, S
dc.contributor.authorAydinli, N
dc.contributor.authorCaliskan, M
dc.contributor.authorTatli, B
dc.date.accessioned2021-03-06T10:02:32Z
dc.date.available2021-03-06T10:02:32Z
dc.date.issued2004
dc.identifier.citationTatli B., Saribeyoglu E., Aydinli N., Caliskan M., Anak S., "Neuroblastoma: An unusual presentation with bilateral ptosis", PEDIATRIC NEUROLOGY, cilt.30, ss.284-286, 2004
dc.identifier.issn0887-8994
dc.identifier.otherav_e8640f55-92d2-447b-8024-4311578f9485
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/152755
dc.identifier.urihttps://doi.org/10.1016/j.pediatrneurol.2003.10.004
dc.description.abstractNeuroblastoma, a common tumor of neural crest origin, demonstrates an extremely variable clinical presentation and behavior. Paraspinal tumors may occur anywhere along the spinal column where they may invade the intervertebral foramina and produce cord compression. Cervical involvement may produce Horner's syndrome. Opsoclonus-myoclonus syndrome is also a well-known neuroimmunologic finding of neuroblastoma. We report a 28-month-old female presenting with ptosis and muscle weakness, diagnosed as having a neuroblastoma. (C) 2004 by Elsevier Inc. All rights reserved.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectTıp
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleNeuroblastoma: An unusual presentation with bilateral ptosis
dc.typeMakale
dc.relation.journalPEDIATRIC NEUROLOGY
dc.contributor.department, ,
dc.identifier.volume30
dc.identifier.issue4
dc.identifier.startpage284
dc.identifier.endpage286
dc.contributor.firstauthorID171307


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