Infantile genetic agranulocytosis, morbus Kostmann: Presentation of six cases from the original “Kostmann family” and a review
- 1 July 2001
- journal article
- review article
- Published by Wiley in Acta Paediatrica
- Vol. 90 (7) , 757-764
- https://doi.org/10.1111/j.1651-2227.2001.tb02801.x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropeniaBlood, 2000
- Cytokine-mobilized allogeneic peripheral blood stem cell transplants in children result in rapid engraftment and a high incidence of chronic GVHDBone Marrow Transplantation, 2000
- Mutations in ELA2, encoding neutrophil elastase, define a 21-day biological clock in cyclic haematopoiesisNature Genetics, 1999
- High incidence of significant bone loss in patients with severe congenital neutropenia (Kostmann’s syndrome)The Journal of Pediatrics, 1997
- Mutations in the granulocyte colony-stimulating factor receptor gene in patients with severe congenital neutropeniaLeukemia, 1997
- Pathophysiology and treatment of severe chronic neutropeniaAnnals of Hematology, 1996
- Mutations in the Gene for the Granulocyte Colony-Stimulating–Factor Receptor in Patients with Acute Myeloid Leukemia Preceded by Severe Congenital NeutropeniaNew England Journal of Medicine, 1995
- Changing Patterns of Infections in the Immunocompromised Patient with CancerHematology/Oncology Clinics of North America, 1993
- Correction of infantile agranulocytosis (Kostmann's syndrome) by allogeneic bone marrow transplantationThe American Journal of Medicine, 1980
- INFANTILE GENETIC AGRANULOCYTOSISActa Paediatrica, 1975