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Neurofibromatosis Type 1 in Children: A Single-Center Experience

dc.contributor.authorULUDAĞ ALKAYA, Dilek
dc.contributor.authorCELKAN, Tülin Tıraje
dc.contributor.authorGunes, Nilay
dc.contributor.authorTÜYSÜZ, Beyhan
dc.contributor.authorAPAK, Hilmi
dc.contributor.authorKacar, Ayse Gonca
dc.contributor.authorKILINÇ OKTAY, Burcu
dc.contributor.authorOzel, Simge Cinar
dc.contributor.authorOCAK, Süheyla
dc.date.accessioned2021-12-10T09:49:36Z
dc.date.available2021-12-10T09:49:36Z
dc.date.issued2021
dc.identifier.citationKacar A. G. , KILINÇ OKTAY B., Ozel S. C. , OCAK S., Gunes N., ULUDAĞ ALKAYA D., TÜYSÜZ B., APAK H., CELKAN T. T. , "Neurofibromatosis Type 1 in Children: A Single-Center Experience", TURKISH ARCHIVES OF PEDIATRICS, cilt.56, sa.4, ss.339-343, 2021
dc.identifier.othervv_1032021
dc.identifier.otherav_14fa4ed0-7066-4590-a414-48211b2e2a75
dc.identifier.urihttp://hdl.handle.net/20.500.12627/168559
dc.identifier.urihttps://doi.org/10.5152/turkarchpediatr.2021.20165
dc.description.abstractObjective: Neurofibromatosis (NF) is the most common autosomal dominantly inherited neurocutaneous syndrome. The characteristic features of NF type 1 (NF-1) are cafe au lait spots, axillary and inguinal freckling, peripheral neurofibromas, optic pathway glioma, and Lisch nodules. The present study aimed to analyze the clinical features of children with NF-1.
dc.language.isoeng
dc.subjectPediatrics
dc.subjectPediatrics, Perinatology and Child Health
dc.subjectHealth Sciences
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleNeurofibromatosis Type 1 in Children: A Single-Center Experience
dc.typeMakale
dc.relation.journalTURKISH ARCHIVES OF PEDIATRICS
dc.contributor.departmentİstanbul Üniversitesi-Cerrahpaşa , ,
dc.identifier.volume56
dc.identifier.issue4
dc.identifier.startpage339
dc.identifier.endpage343
dc.contributor.firstauthorID2694485


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