Dergiler / Turkish Journal of Hematology / 2017 / Cilt: 34 - Sayı: 2

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

Sayfa
186–187
DOI
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Bu Makaleye Atıf Yap

KOPİNSKA, A. J., HELBİG, G., KOCLEGA, A., KYRCZ, S. K. (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, Cilt: 34 - Sayı: 2, 186–187. https://ajindex.com/articles/412751

Kaynakça (9)

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  2. Bing J, Neel A. Two cases of hyperglobulinemia with affection of the central nervous system on a toxi-infection basis. Acta Med Scand 1936;88:492-496
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  6. Frustaci AM, Rusconi C, Picardi P, Veronese S, Montillo M, Cairoli R, Tedeschi A. Bing Neel syndrome in a previously untreated patient with Waldenström’s macroglobulinemia: contribution of MYD88 L265P mutation on cerebrospinal fluid. Clin Lymphoma Myeloma Leuk 2016;1:e7-9
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  9. Castillo JJ, D’Sa S, Lunn MP, Minnema MC, Tedeschi A, Lansigan F, Palomba ML, Varettoni M, Garcia-Sanz R, Nayak L, Lee