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The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action.
Fioredda F, Skokowa J, Tamary H, Spanoudakis M, Farruggia P, Almeida A, Guardo D, Höglund P, Newburger PE, Palmblad J, Touw IP, Zeidler C, Warren AJ, Dale DC, Welte K, Dufour C, Papadaki HA. Fioredda F, et al. Among authors: zeidler c. Hemasphere. 2023 Mar 30;7(4):e872. doi: 10.1097/HS9.0000000000000872. eCollection 2023 Apr. Hemasphere. 2023. PMID: 37008163 Free PMC article.
Congenital neutropenias.
Zeidler C, Schwinzer B, Welte K. Zeidler C, et al. Rev Clin Exp Hematol. 2003 Mar;7(1):72-83. Rev Clin Exp Hematol. 2003. PMID: 14692235 Review.
Severe congenital neutropenia.
Welte K, Zeidler C, Dale DC. Welte K, et al. Among authors: zeidler c. Semin Hematol. 2006 Jul;43(3):189-95. doi: 10.1053/j.seminhematol.2006.04.004. Semin Hematol. 2006. PMID: 16822461 Review.
Severe congenital neutropenia: inheritance and pathophysiology.
Skokowa J, Germeshausen M, Zeidler C, Welte K. Skokowa J, et al. Among authors: zeidler c. Curr Opin Hematol. 2007 Jan;14(1):22-8. doi: 10.1097/00062752-200701000-00006. Curr Opin Hematol. 2007. PMID: 17133096 Review.
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).
Klein C, Grudzien M, Appaswamy G, Germeshausen M, Sandrock I, Schäffer AA, Rathinam C, Boztug K, Schwinzer B, Rezaei N, Bohn G, Melin M, Carlsson G, Fadeel B, Dahl N, Palmblad J, Henter JI, Zeidler C, Grimbacher B, Welte K. Klein C, et al. Among authors: zeidler c. Nat Genet. 2007 Jan;39(1):86-92. doi: 10.1038/ng1940. Epub 2006 Dec 24. Nat Genet. 2007. PMID: 17187068
196 results