MYD88 mutations can be used to identify malignant pleural effusions in Waldenström macroglobulinaemia

Clonal architecture ofCXCR4WHIM-like mutations in Waldenström Macroglobulinaemia

(2015) Lian Xu et al.   BRITISH JOURNAL OF HAEMATOLOGY

MYD88 Mutations and Response to Ibrutinib in Waldenström's Macroglobulinemia

(2015) Steven P. Treon et al.   NEW ENGLAND JOURNAL OF MEDICINE

Extramedullary Waldenström macroglobulinemia

(2014) Ranjit Banwait et al.   AMERICAN JOURNAL OF HEMATOLOGY

Somatic mutations in MYD88 and CXCR4 are determinants of clinical presentation and overall survival in Waldenstrom macroglobulinemia

(2014) S. P. Treon et al.   BLOOD

MYD88L265P mutation contributes to the diagnosis of Bing Neel syndrome

(2014) Stéphanie Poulain et al.   BRITISH JOURNAL OF HAEMATOLOGY

MYD88 L265P in Waldenstrom macroglobulinemia, immunoglobulin M monoclonal gammopathy, and other B-cell lymphoproliferative disorders using conventional and quantitative allele-specific polymerase chain reaction

(2013) L. Xu et al.   BLOOD

MYD88 L265P Somatic Mutation in Waldenström's Macroglobulinemia

(2012) Steven P. Treon et al.   NEW ENGLAND JOURNAL OF MEDICINE