Neurofibromatosis Type 1 in Children: A Single-Center Experience.

Gonca Kaçar, Ayse; Kilinc Oktay, Burcu; Çinar Özel, Simge; Ocak, Süheyla; Günes, Nilay; Uludag Alkaya, Dilek; Tüysüz, Beyhan; Apak, Hilmi; Tiraje Celkan, Tülin

Gonca Kaçar, Ayse; Kilinc Oktay, Burcu; Çinar Özel, Simge; Ocak, Süheyla; Günes, Nilay; Uludag Alkaya, Dilek; Tüysüz, Beyhan; Apak, Hilmi; Tiraje Celkan, Tülin.

Afiliação

Gonca Kaçar A; Department of Pediatric Hematology and Oncology, Istanbul University-Cerrahpasa School of Medicine, Istanbul, Turkey.
Kilinc Oktay B; Department of Genetics, Istanbul University-Cerrahpasa School of Medicine, Istanbul, Turkey.
Çinar Özel S; Department of Pediatric Hematology and Oncology, Istanbul University-Cerrahpasa School of Medicine, Istanbul, Turkey.
Ocak S; Department of Pediatric Hematology and Oncology, Istanbul University-Cerrahpasa School of Medicine, Istanbul, Turkey.
Günes N; Department of Genetics, Istanbul University-Cerrahpasa School of Medicine, Istanbul, Turkey.
Uludag Alkaya D; Department of Genetics, Istanbul University-Cerrahpasa School of Medicine, Istanbul, Turkey.
Tüysüz B; Department of Genetics, Istanbul University-Cerrahpasa School of Medicine, Istanbul, Turkey.
Apak H; Department of Pediatric Hematology and Oncology, Istanbul University-Cerrahpasa School of Medicine, Istanbul, Turkey.
Tiraje Celkan T; Department of Pediatric Hematology and Oncology, Istanbul University-Cerrahpasa School of Medicine, Istanbul, Turkey.

Turk Arch Pediatr ; 56(4): 339-343, 2021 Jul.

Article em En | MEDLINE | ID: mdl-35005728

Palavras-chave

Child; inherited neurocutaneous syndrome; neurofibromatosis; optic glioma

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Screening_studies Idioma: En Revista: Turk Arch Pediatr Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Turquia

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