Cargando…
Bing-Neel Syndrome with Detectable MYD88 L265P Gene Mutation as a Late Relapse Following Autologous Hematopoietic Stem Cell Transplantation for Waldenström’s Macroglobulinemia
Autores principales: | Kopińska, Anna J., Helbig, Grzegorz, Koclęga, Anna, Kyrcz-Krzemień, Sławomira |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440875/ https://www.ncbi.nlm.nih.gov/pubmed/28529201 http://dx.doi.org/10.4274/tjh.2016.0452 |
Ejemplares similares
-
Bing-Neel Syndrome: An Initial Manifestation of Waldenstrom Macroglobulinemia
por: Lee, Matthew S, et al.
Publicado: (2021) -
Therapeutic Experience of Bing-Neel Syndrome Associated with Waldenstrom's Macroglobulinemia
por: Kim, Hyun Do, et al.
Publicado: (2007) -
The Impact of Tirabrutinib Monotherapy for Bing-Neel Syndrome in Waldenström's Macroglobulinemia
por: Sekiguchi, Naohiro
Publicado: (2022) -
Bing-Neel Syndrome, a Rare Presentation of Waldenström Macroglobulinemia—A Multicenter Report by the Polish Lymphoma Research Group
por: Drozd-Sokołowska, Joanna, et al.
Publicado: (2022) -
L265P Mutation of the MYD88 Gene Is Frequent in Waldenström’s Macroglobulinemia and Its Absence in Myeloma
por: Mori, Naoki, et al.
Publicado: (2013)