Mechanisms of Disordered Granulopoiesis in Congenital Neutropenia
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Elsevier
Reference202 articles.
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4. Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease;Ancliff;Blood,2001
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1. Severe congenital neutropenia resulting from G6PC3 deficiency with increased neutrophil CXCR4 expression and myelokathexis;Blood;2010-10-14
2. Genetic Predispositions for Hematologic and Lymphoid Disorders;Molecular Pathology Library;2010
3. Contributions to Neutropenia from PFAAP5 (N4BP2L2), a Novel Protein Mediating Transcriptional Repressor Cooperation between Gfi1 and Neutrophil Elastase;Molecular and Cellular Biology;2009-08-15
4. Congenital Neutropenia Syndromes;Immunology and Allergy Clinics of North America;2008-05
5. Lymphadenopathy as the primary manifestation of malignant transformation in two patients with severe congenital neutropenia;Pediatric Blood & Cancer;2008
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