Ghosal Syndrome – Ten Years Follow-up
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s12098-014-1654-6.pdf
Reference5 articles.
1. Mondal RK, Karmakar B, Chandra PK, Mukherjee K. Ghosal type hemato-diaphyseal dysplasia : a rare variety of engelmann’s disease. Indian J Pediatr. 2007;74:291–3.
2. Ghosal SP, Mukherjee AK, Mukherjee D, Ghosh AK. Diaphyseal dysplasia associated with anemia. J Pediatr. 1988;113:49–57.
3. Gumruk F, Besim A, Altay C. Ghosal haemato-diaphyseal dysplasia: a new disorder. Eur J Pediatr. 1993;152:218–21.
4. Alebouyeh M, Vossough P, Tabarrok F. Early manifestation of Ghosal-type hemato-diaphyseal dysplasia. Pediatr Hematol Oncol. 2003;20:409–15.
5. Vignon-Savoye C, Le Merrer M, Vincens A, Monfort M, Talon P. Ghosal hematodiaphyseal dysplasia: a new case. Arch Pediatr. 2005;12:1244–8.
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1. Ghosal hematodiaphyseal dysplasia – A remediable cause of refractory anemia: A case report;Pediatric Hematology Oncology Journal;2023-12
2. Disorders of Eicosanoid Metabolism;Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases;2022
3. Novel compound heterozygous variants of TBXAS1 presenting with Ghosal hematodiaphyseal dysplasia treated with steroids;Molecular Genetics & Genomic Medicine;2021-02-17
4. Ghosal Hemato-diaphyseal Dysplasia: A Rare Variety of Hypoplastic Anemia with Good Response to Steroid Therapy;Indian Journal of Hematology and Blood Transfusion;2017-04-17
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