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Feasibility of multimodal therapy for rhabdomyosarcoma in a patient with Fukuyama congenital muscular dystrophy.
Sugiyama, Masanaka; Arakawa, Ayumu; Iwata, Shintaro; Tao, Kayoko; Shirakawa, Nami; Watanabe, Yuko; Nakajima, Miho; Yoshida, Akihiko; Ishigaki, Keiko; Kawai, Akira; Ogawa, Chitose.
Afiliação
  • Sugiyama M; Department of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Arakawa A; Department of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Iwata S; Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan.
  • Tao K; Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan.
  • Shirakawa N; Department of Musculoskeletal Oncology and Rehabilitation, National Cancer Center Hospital, Tokyo, Japan.
  • Watanabe Y; Department of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Nakajima M; Department of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Yoshida A; Department of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Ishigaki K; Department of Pediatric Oncology, National Cancer Center Hospital, Tokyo, Japan.
  • Kawai A; Department of Diagnostic Pathology, National Cancer Center Hospital, Tokyo, Japan.
  • Ogawa C; Department of Pediatrics, Tokyo Women's Medical University School of Medicine, Tokyo, Japan.
Pediatr Blood Cancer ; 71(7): e31036, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38679860
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rabdomiossarcoma / Protocolos de Quimioterapia Combinada Antineoplásica Idioma: En Ano de publicação: 2024 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Rabdomiossarcoma / Protocolos de Quimioterapia Combinada Antineoplásica Idioma: En Ano de publicação: 2024 Tipo de documento: Article