Disease: Ghosal hematodiaphyseal dysplasia syndrome
- A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33-34
- Case report: Ghosal hematodiaphyseal dysplasia-A rare cause of skeletal dysplasia and cytopenia
- Chronic steroid-response pancytopenia and increased bone density due to thromboxane synthase deficiency
- Early manifestation of Ghosal-type hemato-diaphyseal dysplasia
- Ghosal haematodiaphyseal dysplasia: a new case
- Ghosal hematodiaphyseal dysplasia with autoimmune anemia in two adult siblings
- Ghosal hematodiaphyseal dysplasia-a concise review including an illustrative patient
- Ghosal Hematodiaphyseal Dysplasia: A Case Report
- Ghosal hematodiaphyseal dysplasia: a rare cause of a myelophthisic anemia
- Ghosal Syndrome--Ten Years Follow-up
- Ghosal type hemato-diaphyseal dysplasia: a rare variety of Engelmann's disease
- Low-dose non-steroidal anti-inflammatory drugs: a promising approach for the treatment of symptomatic bone marrow failure in Ghosal hematodiaphyseal dysplasia
- Nonsteroidal anti-inflammatory drugs as a targeted therapy for bone marrow failure in Ghosal hematodiaphyseal dysplasia
- Novel compound heterozygous variants of TBXAS1 presenting with Ghosal hematodiaphyseal dysplasia treated with steroids
- Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome)