Pediatric erythroblastic transformation of JAK2-mutated prefibrotic primary myelofibrosis with concurrent PHF6 mutations.

Oshiro, Tokiko; Hamada, Satoru; Kiyuna, Sinobu; Sakiyama, Hideki; Hyakuna, Nobuyuki; Tamaki, Tomoko; Muramatsu, Hideki; Nakanishi, Koichi

Oshiro, Tokiko; Hamada, Satoru; Kiyuna, Sinobu; Sakiyama, Hideki; Hyakuna, Nobuyuki; Tamaki, Tomoko; Muramatsu, Hideki; Nakanishi, Koichi.

Afiliación

Oshiro T; Department of Pediatrics, University of Ryukyus Hospital, Nakagami-gun, Japan.
Hamada S; Department of Pediatrics, University of Ryukyus Hospital, Nakagami-gun, Japan.
Kiyuna S; Department of Pediatrics, University of Ryukyus Hospital, Nakagami-gun, Japan.
Sakiyama H; Department of Pediatrics, University of Ryukyus Hospital, Nakagami-gun, Japan.
Hyakuna N; Okinawa Prefectural Red Cross Blood Center, Naha, Japan.
Tamaki T; Department of Pathology and Oncology, Graduate School of Medicine, University of Ryukyus, Nakagami-gun, Japan.
Muramatsu H; Department of Pediatrics, Graduate School of Medicine, University of Nagoya, Nagoya, Japan.
Nakanishi K; Department of Pediatrics, Graduate School of Medicine, University of The Ryukyus, Nakagami-gun, Japan.

Pediatr Blood Cancer ; 70(10): e30508, 2023 10.

Article en En | MEDLINE | ID: mdl-37337098

Asunto(s)

Mielofibrosis Primaria; Humanos; Médula Ósea; Calreticulina/genética; Janus Quinasa 2/genética; Mutación; Mielofibrosis Primaria/genética; Proteínas Represoras/genética; Masculino; Adolescente

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mielofibrosis Primaria Límite: Adolescent / Humans / Male Idioma: En Revista: Pediatr Blood Cancer Asunto de la revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Año: 2023 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos

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