Soft tissue sarcomas and central nervous system tumors in children with neurofibromatosis type 1.

Cecen E., İNCE D., Uysal K. M., ÖZER E., Cetingoz R., Ozguven A. A., ...Daha Fazla

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, cilt.27, sa.11, ss.1885-93, 2011 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 27 Sayı: 11
  • Basım Tarihi: 2011
  • Doi Numarası: 10.1007/s00381-011-1425-x
  • Dergi Adı: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1885-93
  • Anahtar Kelimeler: Neurofibromatosis type 1, Childhood, Cancer, Central nervous system tumors, Optic glioma, Malignant peripheral nerve sheath tumors, Sarcoma, OPTIC PATHWAY GLIOMAS, SHEATH TUMORS, SPONTANEOUS REGRESSION, FOLLOW-UP, NF1 GENE, RHABDOMYOSARCOMA, GLIOBLASTOMA, MANAGEMENT, PATIENT
  • Dokuz Eylül Üniversitesi Adresli: Evet

Özet

Objects We aim to evaluate the characteristics of pediatric patients with neurofibromatosis type 1 (NF1) who developed soft tissue sarcomas (STSs) and central nervous system(CNS) tumors that have been followed up in our center.