Bing-Neel Syndrome with Detectable MYD88 L265P Gene Mutation as a Late Relapse Following Autologous Hematopoietic Stem Cell Transplantation for Waldenström’s Macroglobulinemia

Apply

Bing-Neel Syndrome with Detectable MYD88 L265P Gene Mutation as a Late Relapse Following Autologous Hematopoietic Stem Cell Transplantation for Waldenström’s Macroglobulinemia

Journal Title: Turkish Journal of Hematology - Year 2017, Vol 34, Issue 2

Abstract

To the Editor,

Authors and Affiliations

Anna J. Kopińska, Grzegorz Helbig, Anna Koclęga, Sławomira Kyrcz-Krzemień

Keywords

Three Novel Calreticulin Mutations in Two Turkish Patients

Ritüksimab İlişkili Geridönüşlü Hepatosellüler Hasar

Niemann - Pick disease associated with hemophagocytic syndrome

Hemophagocytic lymphohistiocytosis (HLH) is a disease characterized by phagocytosis of blood cells by macrophages within the lymphoreticular tissue. It can develop secondary to some diseases or be familial as a result of...

Iron and Zinc Treatment in Iron Deficiency

Acute Myocardial Infarction Due to Eltrombopag Therapy in a Patient with Immune Thrombocytopenic Purpura

EP ID EP228530
DOI 10.4274/tjh.2016.0452
Views 73
Downloads 0

How To Cite

Anna J. Kopińska, Grzegorz Helbig, Anna Koclęga, Sławomira Kyrcz-Krzemień (2017). Bing-Neel Syndrome with Detectable MYD88 L265P Gene Mutation as a Late Relapse Following Autologous Hematopoietic Stem Cell Transplantation for Waldenström’s Macroglobulinemia. Turkish Journal of Hematology, 34(2), 186-187. https://europub.co.uk./articles/-A-228530