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Whole-body MRI evaluation in neurofibromatosis type 1 patients younger than 3 years old and the genetic contribution to disease progression.
Kang, Eungu; Kim, Yoon-Myung; Choi, Yunha; Lee, Yena; Kim, JunYoung; Choi, In Hee; Yoo, Han-Wook; Yoon, Hee Mang; Lee, Beom Hee.
Afiliación
  • Kang E; Department of Pediatrics, Korea University Ansan Hospital, Korea University College of Medicine, Ansan, Korea.
  • Kim YM; Department of Pediatrics, Gangneung Asan Hospital, Gangneung, Korea.
  • Choi Y; Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, 88, Olympic-ro 43-Gil, Songpa-Gu, Seoul, 05505, Korea.
  • Lee Y; Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, 88, Olympic-ro 43-Gil, Songpa-Gu, Seoul, 05505, Korea.
  • Kim J; Department of Genetic Counseling, University of Ulsan College of Medicine, Seoul, Korea.
  • Choi IH; Department of Genetic Counseling, University of Ulsan College of Medicine, Seoul, Korea.
  • Yoo HW; Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, 88, Olympic-ro 43-Gil, Songpa-Gu, Seoul, 05505, Korea.
  • Yoon HM; Medical Genetics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Lee BH; Department of Radiology and Research Institute of Radiology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-Gil, Songpa-Gu, Seoul, 05505, Korea. espoirhm@gmail.com.
Orphanet J Rare Dis ; 17(1): 24, 2022 01 29.
Article en En | MEDLINE | ID: mdl-35093157
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neurofibromatosis 1 Tipo de estudio: Observational_studies Límite: Child / Humans Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
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PubMed Links
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neurofibromatosis 1 Tipo de estudio: Observational_studies Límite: Child / Humans Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2022 Tipo del documento: Article