Conradi NG et al. |
Reactions of vessel walls and brain parenchyma to the accumulation of Gaucher cells in the Norrbottnian type (type III) of Gaucher disease. |
1988 |
Acta Neuropathol. |
pmid:3364161
|
Soffer D et al. |
Central nervous system involvement in adult-onset Gaucher's disease. |
1980 |
Acta Neuropathol. |
pmid:7355669
|
Conradi NG et al. |
Neuropathology of the Norrbottnian type of Gaucher disease. Morphological and biochemical studies. |
1984 |
Acta Neuropathol. |
pmid:6524300
|
Smith RL et al. |
Unusual cardiac, renal and pulmonary involvement in Gaucher's disease. Intersitial glucocerebroside accumulation, pulmonary hypertension and fatal bone marrow embolization. |
1978 |
Am. J. Med. |
pmid:686020
|
Kaye EM et al. |
Type 2 and type 3 Gaucher disease: a morphological and biochemical study. |
1986 |
Ann. Neurol. |
pmid:3752966
|
Daniels LB et al. |
Brain glucocerebrosidase in Gaucher's disease. |
1982 |
Arch. Neurol. |
pmid:6810854
|
Nishimura RN and Barranger JA |
Neurologic complications of Gaucher's disease, type 3. |
1980 |
Arch. Neurol. |
pmid:6766716
|
Shoenfeld Y et al. |
Gaucher's disease: a disease with chronic stimulation of the immune system. |
1982 |
Arch. Pathol. Lab. Med. |
pmid:7049116
|
Nilsson O et al. |
The occurrence of psychosine and other glycolipids in spleen and liver from the three major types of Gaucher's disease. |
1982 |
Biochim. Biophys. Acta |
pmid:7126619
|
Beutler E |
Gaucher disease. |
1988 |
Blood Rev. |
pmid:3289655
|
Poll LW et al. |
Response of Gaucher bone disease to enzyme replacement therapy. |
2002 |
Br J Radiol |
pmid:12036830
|
Adar T et al. |
Aggregation of red blood cells in patients with Gaucher disease. |
2006 |
Br. J. Haematol. |
pmid:16827817
|
Schaison G et al. |
[French results of enzyme replacement therapy in Gaucher's disease]. |
2002 |
Bull. Acad. Natl. Med. |
pmid:12412377
|
Harzer K et al. |
Concurrent increase of cholesterol, sphingomyelin and glucosylceramide in the spleen from non-neurologic Niemann-Pick type C patients but also patients possibly affected with other lipid trafficking disorders. |
2003 |
FEBS Lett. |
pmid:12606053
|
Pilz H and Heipertz R |
[Differential diagnosis of congenital lipidoses by lipid analyses of body fluids, biopsy and autopsy tissue]. |
1975 |
Fortschr Neurol Psychiatr Grenzgeb |
pmid:53174
|
Campbell PE et al. |
A model of neuronopathic Gaucher disease. |
2003 |
J. Inherit. Metab. Dis. |
pmid:14707511
|
Dawson G et al. |
Distribution of glycosphingolipids in the serum lipoproteins of normal human subjects and patients with hypo- and hyperlipidemias. |
1976 |
J. Lipid Res. |
pmid:178813
|
Hara A et al. |
Abnormalities of glycosphingolipids in mucopolysaccharidosis type III B. |
1984 |
J. Lipid Res. |
pmid:6423755
|
Erickson JS and Radin NS |
N-hexyl-O-glucosyl sphingosine, an inhibitor of glucosyl ceramide -glucosidase. |
1973 |
J. Lipid Res. |
pmid:4698260
|
Nilsson O and Svennerholm L |
Accumulation of glucosylceramide and glucosylsphingosine (psychosine) in cerebrum and cerebellum in infantile and juvenile Gaucher disease. |
1982 |
J. Neurochem. |
pmid:7097276
|