Persistent pseudo-Pelger-Huët anomaly
- PMID: 32862285
- DOI: 10.1007/s00277-020-04242-9
Persistent pseudo-Pelger-Huët anomaly
References
-
- Zia A, Fışgin T, Sokolowski C, Tanner SM, Savaşan S (2012) Acute lymphoblastic leukemia and vitamin B12 deficiency secondary to a gastric intrinsic factor gene mutation. Pediatr Blood Cancer 59(4):766–767 - DOI
-
- Sturm AC, Baack EC, Armstrong MB, Schiff D, Zia A, Savasan S, de la Chapelle A, Tanner SM (2013) Hereditary intrinsic factor deficiency in Chaldeans. JIMD Rep 7:13–18 - DOI
-
- Isaac McGraw B, Sweeney C, Savaşan S (2018) Recurrent urinary tract infections and low secretory IgA following CD19-directed CAR T-cell therapy for relapsed acute lymphoblastic leukemia. Pediatr Blood Cancer 65(1). https://doi.org/10.1002/pbc.26739
-
- Best S, Salvati F, Kallo J, Garner C, Height S, Thein SL, Rees DC (2003) Lamin B-receptor mutations in Pelger-Huët anomaly. Br J Haematol 123(3):542–544 - DOI
-
- Jaén A, Irriguible D, Milla F, Vallespi T, Torrabadella M, Abella E, Lafuente R, Woessner S (1990) Abnormal chromatin clumping in leucocytes: a clue to a new subtype of myelodysplastic syndrome. Eur J Haematol 45:209–214 - DOI
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
