Niemann-Pick disease: Lipid storage in bone marrow macrophages

The Histochemical Journal

Volumn 15, Issue 11, 1983, Pages 1065-1077

  Elleder, M ^a   Hrodek, J ^a   Cihula J ^a  

^a CHARLES UNIVERSITY   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD AND HEMOPOIETIC SYSTEM; BONE MARROW; CLINICAL ARTICLE; CONGENITAL DISORDER; CYTOLOGY; DIAGNOSIS; HISTOLOGY; HUMAN; LIPID STORAGE; MACROPHAGE; NIEMANN PICK DISEASE;

ADOLESCENT; ADULT; BONE MARROW; BONE MARROW CELLS; CHILD; FEMALE; HISTOCYTOCHEMISTRY; HUMAN; LIPIDS; LYSOSOMES; MACROPHAGES; MALE; MIDDLE AGE; NIEMANN-PICK DISEASES; PHOSPHOLIPIDS; SPHINGOMYELINS;

EID: 0020964639     PISSN: 00182214     EISSN: 15736865     Source Type: Journal    
DOI: 10.1007/BF01003970     Document Type: Article

References (42)

1. Sphingomyelinase defect in Niemann-Pick disease, type C, fibroblasts
2. Niemann-Pick's Disease
3. Isoenzymes of sphingomyelinase and the genetic defect in Niemann-Pick disease
4. Niemann-Pick disease, type C: evidence for the deficiency of an activating factor stimulating sphingomyelin and glucocerebroside degradation
5. Niemann-Pick's disease: a review of eighteen patients
6. Lipidhistochemistry—a critical survey
7. Studies in lipid histochemistry. VI. Problems of extraction with acetone in lipid histochemistry
8. Studies in lipid histochemistry. XI. New, rapid, simple and selective method for the demonstration of phospolipids
9. Studies in lipid histochemistry. XII. Histochemical detection of sphingomyelin
10. Neuropathology of various types of Niemann-Pick disease
11. Niemann-Pick disease. Analysis of liver tissue in sphingomyelinase-deficient patients
12. Familiar hemophagocytic reticulosis
13. Chylomikrons and the formation of foam cells in type I hyperlipoproteinemia
14. Fabry's disease—glycolipid lipidosis. Histochemical and electronmicroscopic studies of two cases
15. Progressive paralysis of vertical gaze in lipid storage disease
16. Resolution of tissue sphingomyelinase isoelectric profile in multiple components is extraction dependent: evidence for a component defect in Niemann-Pack disease type C is spurious
17. Sphingomyelinoses (Niemann-Picksche Erkrankung)
18. Morbus Niemann-Pick B—enzymatisch gesichert-mit unerwarteter retinaler Beteiligung
19. Ceroid storage in a child with a Niemann-Pick type syndrome
20. Gaucher cells in chronic myelocytic leukemia: an acquired abnormality
21. 1 gangliosidosis
22. Metabolic disoorders: general considerations
23. Thrombocytopenic purpura with histiocytosis of the spleen
24. Lymphadenitis with massive hemophagocytic sinus histiocytosis
25. Familial hemofagocytic lymphohistiocytosis
26. A neurovisceral storage disease with vertical supranuclear ophthalmoplegia and its relationship to Niemann-Pick disease—a report of nine cases
27. The juvenile form of Niemann-Pick disease
28. Sea-blue histiocytosis associated with hyperlipidaemia
29. Wolman's disease
30. Maladie de Niemann-Pick type “C” de Crocker. Etude ultrastructurele dún cas
31. Niemann-Pick disease. Morphological and biochemical studies in the visceral form with late central nervous system involvement (Crocker's group C)
32. Splenic lipidosis. Histochemical and ultrastructural differentiation with special reference to the syndrome of the sea-blue
33. Hyperlipoproteinemia. A review of the five types with first report on necropsy findings in type 3
34. Sinus histiocytosis with massive lymphadenopathy — a pseudolymphomatous benign disorder. Analysis of 34 cases
35. Figures myeliniques dans les cellules spumeuses de la maladie de Fabry
36. Sphingomyelinase activities of various human tissues in control subjects and in Niemann-Pick disease—development and evaluation of a microprocedure
37. Genetic and demographic aspects of Nova Scotia Niemann-Pick disease (type D)