Ghosal hematodiaphyseal dysplasia: A rare cause of a myelophthisic anemia
- 29 July 2010
- journal article
- case report
- Published by Wiley in Pediatric Blood & Cancer
- Vol. 55 (6), 1187-1190
- https://doi.org/10.1002/pbc.22662
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome)Nature Genetics, 2008
- Ghosal type hemato-diaphyseal dysplasia: A rare variety of Engelmann’s diseaseIndian Journal of Pediatrics, 2007
- A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33–34Human Genetics, 2007
- Un nouveau cas de dysplasie hématodiaphysaire de GhosalArchives de Pédiatrie, 2005
- Effects of selective prostaglandin EP2 and EP4 receptor agonists on bone resorption and formation in fetal rat organ culturesProstaglandins & Other Lipid Mediators, 2003
- Early Manifestation of Ghosal-Type Hemato-Diaphyseal DysplasiaPediatric Hematology and Oncology, 2003
- Ghosal haemato-diaphyseal dysplasia: A new disorderEuropean Journal of Pediatrics, 1993
- Prostaglandin-mediated suppression of in vitro growth of erythroid progenitor cellsKidney International, 1989
- High-dose intravenous methylprednisolone therapy for anemia associated with diaphyseal dysplasiaThe Journal of Pediatrics, 1989
- Diaphyseal dysplasia associated with anemiaThe Journal of Pediatrics, 1988