Type 2 and type 3 Gaucher disease: A morphological and biochemical study

Annals of Neurology

Volumn 20, Issue 2, 1986, Pages 223-230

  Kaye, Edward M ^a,c   Ullman, M David ^b,c   Wilson, Edward R ^d   Barranger, John A ^e  

^a Education and Clinical Center   (United States)

^b VETERANS AFFAIRS MEDICAL CENTER   (United States)

^c BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^e NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSYLCERAMIDE;

AUTOPSY; BRAIN STEM; CASE REPORT; CENTRAL NERVOUS SYSTEM; CEREBELLUM CORTEX; CORPUS STRIATUM; DENTATE NUCLEUS; DIAGNOSIS; FRONTAL CORTEX; GAUCHER DISEASE; HISTOLOGY; HUMAN; INFANT; OCCIPITAL CORTEX; PRIORITY JOURNAL; TEMPORAL CORTEX; THALAMUS;

BRAIN; BRAIN STEM; CEREBELLUM; CEREBRAL CORTEX; CEREBROSIDES; CORPUS STRIATUM; DIENCEPHALON; FEMALE; GAUCHER DISEASE; GLIOSIS; HUMAN; INFANT; MALE; SUPPORT, U.S. GOV'T, NON-P.H.S.;

EID: 0022494415     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.410200208     Document Type: Article

References (31)

1. Fine structure of central nervous system in early infantile Gaucher's disease
2. The cerebral pathology of infantile Gaucher's disease
3. Glucosylceramide lipidosis: Gaucher's disease
4. Maladie de Gaucher au nourrisson
5. Acute infantile Gaucher's disease in identical twins: an account of clinical and neuropathologic observations
6. A simple method for the isolation and purification of total lipids from animal tissues
7. Lipid composition of the brain in infantile Gaucher's disease
8. Mutations of glucocerebrosidase: discrimination of neurologic and non‐neurologic phenotypes of Gaucher disease
9. Determination of Gaucher's disease phenotypes with monoclonal antibody
10. Isolation of cDNA clones for human β‐glucocerebrosidase using the g + 11 expression system
11. Infantile Gaucher's disease: a biochemical study
12. Infantile neurological Gaucher's disease in three siblings: an ultrastructural study
13. Separation and quantitation of perbenzoylated glucocerebroside and galactocerebroside by high performance liquid chromatography
14. Über morbus Gaucher mit hirnveranderungen im Sauglingsalter
15. Studies of neural and visceral glycolipids in a case of infantile form of Gaucher's disease
16. Protein measurement with the Folin phenol reagent
17. A case of juvenile Gaucher's disease with intraneuronal lipid storage
18. Accumulation of glucosylceramide and glucosylsphingosine (psychosine) in cerebrum and cerebellum in infantile and juvenile Gaucher disease
19. Neurologic complications of Gaucher's disease, type 3
20. The neuropathology of infantile Gaucher's disease
21. La maladie de Gaucher chez le nourrisson
22. Isolation and characterization of the principal cerebral glycolipids in the infantile and adult forms of Gaucher's disease
23. Lipid class composition of normal human brain and variations in metachromatic leukodystrophy, Tay‐Sachs, Niemann Pick, chronic Gaucher's and Alzheimer's diseases
24. Ein weiterer Fall von morbus Gaucher beim Saugling
25. Die Gehirnveranderungen beim morbus Gaucher des Sauglings
26. Brain glycolipids in infantile Gaucher's disease
27. Quantitative analysis of plasma neutral glycosphingolipids by high performance liquid chromatography of their perbenzoyl derivatives
28. Quantitative microanalysis of perbenzoylated neurtral glycosphingolipids by high performance liquid chromatography with detection at 230 nm
29. Chemical pathology of Krabbe disease: the occurrence of psychosine and other neutral sphingoglycolipids
30. Vascular involvement in type 3 neuronopathic Gaucher's disease
31. Noninfantile neuronopathic Gaucher's disease: a clinicopathologic study