Results 261 to 270 of about 9,391,147 (295)
Cost-effectiveness analysis of ambroxol for the treatment of Chinese patients with Gaucher disease. [PDF]
Front Med (Lausanne)Huang Y, Yuan H, Huang Z.
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Home Enzyme Replacement Therapy in Gaucher Disease: A Review. [PDF]
J Clin MedKieć-Wilk B +6 more
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Generation and Treatment of a Novel Severe Model of Visceral Gaucher Disease by Genetic Therapy. [PDF]
PharmaceuticsGeard AF +5 more
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Cultured Macrophage Models for the Investigation of Lysosomal Glucocerebrosidase and Gaucher Disease. [PDF]
Int J Mol SciLouwerse M +7 more
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New England Journal of Medicine, 1987
Traditionally, Gaucher's disease has been divided into three clinical forms, which have recently been reviewed.1 , 2 Type 1 disease is a non-neuronopathic, chronic disorder characterized by hypersp...
M, Lev, K S, Sundaram
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Traditionally, Gaucher's disease has been divided into three clinical forms, which have recently been reviewed.1 , 2 Type 1 disease is a non-neuronopathic, chronic disorder characterized by hypersp...
M, Lev, K S, Sundaram
+7 more sources
The Lancet, 2001
Correspondence to: Dr Deborah Elstein (e-mail: zimran@md2.huji.ac.il) reduced enzyme activity with accumulation of glucosylceramide in the macrophages of the reticuloendothelial system. Three clinical subtypes of Gaucher’s disease have been described on the basis of the absence (type I) or presence (types II and III) of a neurological component (panel).
D, Elstein +3 more
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Correspondence to: Dr Deborah Elstein (e-mail: zimran@md2.huji.ac.il) reduced enzyme activity with accumulation of glucosylceramide in the macrophages of the reticuloendothelial system. Three clinical subtypes of Gaucher’s disease have been described on the basis of the absence (type I) or presence (types II and III) of a neurological component (panel).
D, Elstein +3 more
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Gastroenterology, 1955
Summary 1. A case of Gaucher's disease is described in a young adult who had no symptoms referable to this condition. 2. The diagnosis was established by liver biopsy examination, a method not previously discussed in relation to this disease.
P, EDLIN, W E, KEPLER, G W, KNABE
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Summary 1. A case of Gaucher's disease is described in a young adult who had no symptoms referable to this condition. 2. The diagnosis was established by liver biopsy examination, a method not previously discussed in relation to this disease.
P, EDLIN, W E, KEPLER, G W, KNABE
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The Indian Journal of Pediatrics, 1973
1. The literature regarding Gaucher's discase is briefly reviewed. 2. Clinico-pathological findings of a fatal case of Gaucher's disease in an infant are recorded. 3. The predominant accumulation of galacto-cerebroside in the splcen observed on chemical analysis is commented upon. 4.
N K, Patoria +4 more
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1. The literature regarding Gaucher's discase is briefly reviewed. 2. Clinico-pathological findings of a fatal case of Gaucher's disease in an infant are recorded. 3. The predominant accumulation of galacto-cerebroside in the splcen observed on chemical analysis is commented upon. 4.
N K, Patoria +4 more
openaire +2 more sources
New England Journal of Medicine, 1991
PHYSICIANS often regard Gaucher's disease as a rare, esoteric, untreatable disorder. Fortunately, the more severe forms of the disease are indeed quite uncommon, but milder forms of Gaucher's disease are encountered frequently, particularly in the Jewish population.
Jane F. Desforges, Ernest Beutler
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PHYSICIANS often regard Gaucher's disease as a rare, esoteric, untreatable disorder. Fortunately, the more severe forms of the disease are indeed quite uncommon, but milder forms of Gaucher's disease are encountered frequently, particularly in the Jewish population.
Jane F. Desforges, Ernest Beutler
openaire +5 more sources