Literature DB >> 382486

Attempt at enzyme replacement by organ transplantation: renal transplantation in Gaucher disease.

C G Groth, H Collste, S Dreborg, G Håkansson, G Lundgren, L Svennerholm.   

Abstract

Following renal transplantation, hepatic glucocerebroside deposits in a child with Gaucher disease were reduced. This suggests that enzyme replacement had been achieved.

Entities:  

Mesh：

Substances：

Year:  1979        PMID： 382486

Source DB:  PubMed          Journal:  Transplant Proc        ISSN： 0041-1345            Impact factor:   1.066


  3 in total

1.  The correction of Hunter fibroblasts by exogenous iduronate sulfate sulfatase: biochemical and ultrastructural studies.

Authors:  R Eliahu; E Sekeles; R Cohen; G Bach
Journal:  Am J Hum Genet       Date:  1981-07       Impact factor: 11.025

2.  Gaucher disease--Norrbottnian type. I. General clinical description.

Authors:  S Dreborg; A Erikson; B Hagberg
Journal:  Eur J Pediatr       Date:  1980-03       Impact factor: 3.183

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

Authors:  J Sorge; W Kuhl; C West; E Beutler
Journal:  Proc Natl Acad Sci U S A       Date:  1987-02       Impact factor: 11.205
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.