(Q35331218)

7 August 2017

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title

Alglucerase. A review of its therapeutic use in Gaucher's disease (English)

1 reference

7 August 2017

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R. Whittington

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1379912

20 September 2022

K. L. Goa

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1379912

20 September 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1379912

20 September 2022

publication date

1 July 1992

1 reference

7 August 2017

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7 August 2017

44

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7 August 2017

72-93

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7 August 2017

1

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https://scigraph.springernature.com/pub.10.2165/00003495-199244010-00007

7 August 2017

0 references

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Isolation and Characterization of Glucocerebrosidase from Human Placental Tissue

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Cutaneous manifestations of Gaucher disease

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Glucocerebrosidase processing in normal fibroblasts and in fibroblasts from patients with type I, type II, and type III Gaucher disease

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A 27-year experience with splenectomy for Gaucher's disease

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An improved procedure for diagnosis of Gaucher disease using cultured skin fibroblasts and the chromogenic substrate, 2-hexadecanoylamino-4-nitrophenyl-beta-D-glucopyranoside

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Correction of glucocerebrosidase deficiency after retroviral-mediated gene transfer into hematopoietic progenitor cells from patients with Gaucher disease

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Norrbottnian type of Gaucher disease--clinical, biochemical and molecular biology aspects: successful treatment with bone marrow transplantation

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Heritable catabolic and anabolic disorders of lipid metabolism

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Gaucher's disease: a disease with chronic stimulation of the immune system

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Unusual cardiac, renal and pulmonary involvement in Gaucher's disease. Intersitial glucocerebroside accumulation, pulmonary hypertension and fatal bone marrow embolization

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Dose-dependent responses to macrophage-targeted glucocerebrosidase in a child with Gaucher disease

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Assay of glucocerebrosidase using a fluorescent analogue of glucocerebroside for the diagnosis of Gaucher disease

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High frequency of the Gaucher disease mutation at nucleotide 1226 among Ashkenazi Jews

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Skeletal complications of Gaucher disease

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The assay of glucocerebrosidase activity using the natural substrata

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Lectin-specific targeting of lysosomal enzymes to reticuloendothelial cells

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Activity of glucocerebrosidase in extracts of different cell types from type 1 Gaucher disease patients

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Renal transplantation in Type II Gaucher disease

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The uptake of native and desialylated glucocerebrosidase by rat hepatocytes and Kupffer cells

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Replacement therapy for inherited enzyme deficiency--macrophage-targeted glucocerebrosidase for Gaucher's disease

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Activator protein deficient Gaucher's disease. A second patient with the newly identified lipid storage disorder

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Newer aspects of some interesting lipid storage diseases: Tay-Sachs and Gaucher's diseases

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Gaucher's disease: a review, and discussion of twenty cases

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Pulmonary hypertension and Gaucher's disease: logical association or mere coincidence?

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Biosynthesis and maturation of glucocerebrosidase in Gaucher fibroblasts

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Gaucher's disease complicated by bleeding esophageal varices and colonic infiltration by Gaucher cells

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Comparative study on glucocerebrosidase in spleens from patients with Gaucher disease

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Enzyme replacement therapy in Gaucher's disease: large-scale purification of glucocerebrosidase suitable for human administration

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Targeting of synthetically glycosylated human placental glucocerebrosidase

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Gaucher disease type III (Norrbottnian type) is caused by a single mutation in exon 10 of the glucocerebrosidase gene

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Gaucher disease: a century of delineation and research. Enzyme replacement therapy: model and clinical studies

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Complete correction of the enzymatic defect of type I Gaucher disease fibroblasts by retroviral-mediated gene transfer

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Enzyme replacement therapy for Gaucher disease

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Gaucher's disease and chronic lymphocytic leukemia. Possible pathogenetic link between Gaucher's disease and B-cell proliferations?

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Gaucher cells in chronic myelocytic leukemia: an acquired abnormality

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12 December 2020

Therapeutic response to intravenous infusions of glucocerebrosidase in a patient with Gaucher disease

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12 December 2020

Accumulation of glucosylceramide and glucosylsphingosine (psychosine) in cerebrum and cerebellum in infantile and juvenile Gaucher disease

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12 December 2020

Gaucher disease of the Norrbottnian type (type III). Phenotypic manifestations

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12 December 2020

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

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12 December 2020

Hematologic improvement in a patient with Gaucher disease on long-term enzyme replacement therapy: evidence for decreased splenic sequestration and improved red blood cell survival

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12 December 2020

10.2165/00003495-199244010-00007

Identifiers

DOI

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Dimensions Publication ID

7 August 2017

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