• A Case with Gaucher-Like Cells
• A mutation in the saposin C domain of the sphingolipid activator protein (Prosaposin) gene causes neurodegenerative disease in mice
• A novel mutation in the coding region of the prosaposin gene leads to a complete deficiency of prosaposin and saposins, and is associated with a complex sphingolipidosis dominated by lactosylceramide accumulation
• A Rare Case of Hemoglobin E Hemoglobinopathy with Gaucher's Disease
• A Type 3 Gaucher-Like Disease Due To Saposin C Deficiency in Two Emirati Families Caused by a Novel Splice Site Variant in the PSAP Gene
• Abundant hepatic Gaucher-like cells following chemotherapy and bone marrow transplantation for hematologic malignancy: report of two cases
• Accumulation of tissue glucosylsphingosine in Gaucher-like mouse induced by the glucosylceramidase inhibitor cyclophellitol
• Acquired lipidosis of marrow macrophages: birefringent blue crystals and Gaucher-like cells, sea-blue histiocytes, and grey-green crystals
• Acquired lipidosis: Gaucher-like cells and "blue cells" in chronic granulocytic leukemia
• Angulate lysosomes
• Association Between Progranulin and Gaucher Disease
• Clinical features of adult GM1 gangliosidosis: report of three Indian patients and review of 40 cases
• Coexistence of Gaucher Disease and Philadelphia positive chronic granulocytic leukemia
• D409H/D409H genotype in Gaucher-like disease
• Gaucher-like cells in a granular cell tumor
• Gaucher-like cells in juvenile GM1-gangliosidosis and in beta-thalassemia -- A histochemical and ultrastructural observation
• Gaucher-like cells in the spleen in Werlhof's disease
• Gaucher-like cells in the spleen of an adult subject with Cooley's disease
• Gaucher-like cells in the spleen of an adult with Cooley's anaemia
• Gaucher-like changes in human blood-derived macrophages induced by beta-glucocerebrosidase inhibition
• Gaucheroid structures in macrophages in lipomelanic reticulosis
• Lymphoplasmacytic lymphoma with monoclonal gammopathy-related pseudo-Gaucher cell infiltration in bone marrow and spleen--diagnostic and therapeutic dilemmas
• Pathological, histochemical and ultrastructural studies on sea-blue histiocytes and Gaucher-like cells in acquired lipidosis occurring in leukemia
• Periosteal Gaucher-like cells in beta-thalassemia major
• Phagocytosis of Erythrocytes from Gaucher Patients Induces Phenotypic Modifications in Macrophages, Driving Them toward Gaucher Cells
• Presence of Gaucher-like cells in a case of Ph1-positive chronic myeloid leukemia with lymphoid-myeloid crisis
• Pseudo-Gaucher cells in disseminated mycobacterial infection
• Pseudo-Gaucher cells in multiple myeloma
• Pseudo-Gaucher cells preceding the appearance of immunoblastic lymphoma
• Pseudo-Gaucher's cells in association with common acute lymphoblastic leukemia
• Pseudogaucher cells obscuring multiple myeloma: a case report
• Sixteen years of prenatal consultations for the N370S/N370S Gaucher disease genotype: what have we learned?
• Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: biochemical signs of combined sphingolipidoses
• Thalassaemia Trait with Gaucher Disease: A Diagnostic Dilemma
• The role of saposin C in Gaucher disease