Aberrant bone marrow vascularization patterns in untreated patients with Gaucher disease type 1
Author:
Funder
Regional Agreement on Medical Training and Clinical Research
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference27 articles.
1. Phenotype, diagnosis, and treatment of Gaucher's disease;Grabowski;Lancet,2008
2. Gaucher disease: mutation and polymorphism spectrum in the glucocerebrosidase gene (GBA);Hruska;Hum. Mutat.,2008
3. Phenotypic characterization of large populations from the ICGG Gaucher Registry;Grabowski;Am. J. Hematol.,2015
4. Clinical utility of different bone marrow examination methods in the diagnosis of adults with sporadic Gaucher disease type 1;Machaczka;Pol. Arch. Med. Wewn.,2014
5. Atypical cytomorphology of Gaucher cells is frequently seen in bone marrow smears from untreated patients with Gaucher disease type 1;Markuszewska-Kuczyńska;Folia Histochem. Cytobiol.,2015
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3. Vascular endothelial growth factor (VEGF), tissue inhibitors of metalloproteinase-1 (TIMP-1) and nail fold capillaroscopy changes in children and adolescents with Gaucher disease; relation to residual disease severity;Cytokine;2020-09
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