Literature DB >> 8544959

Enzyme infusion therapy of the Norrbottnian (type 3) Gaucher disease.

A Erikson1, M Aström, J E Månsson.   

Abstract

We report our experience from enzyme infusion therapy of eight patients with the Norrbottnian type of Gaucher disease (type 3) aged 4 to 42 years. All patients responded with increased well-being, decreased liver and spleen size and normalized hematological parameters. The children caught up in growth. No further neurological deterioration occurred and there were some indications of neurological improvement. Circulating glucosylceramide concentrations seemed to be a possible parameter to monitor the dosage of infused enzyme. The circulating glucosylceramide levels responded better in non-splenectomized patients. Enzyme infusion therapy can be recommended in type 3 Gaucher disease.

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Year:  1995        PMID: 8544959     DOI: 10.1055/s-2007-979754

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  9 in total

1.  Enzyme replacement therapy in type III Gaucher disease.

Authors:  A Tylki-Szymańska; B Czartoryska
Journal:  J Inherit Metab Dis       Date:  1999-04       Impact factor: 4.982

Review 2.  Remaining problems in the management of patients with Gaucher disease.

Authors:  A Erikson
Journal:  J Inherit Metab Dis       Date:  2001       Impact factor: 4.982

3.  Neurological outcome of a patient with Gaucher disease type III treated by enzymatic replacement therapy.

Authors:  D Dobbelaere; S Sukno; S Defoort-Dhellemmes; M D Lamblin; C Largillière
Journal:  J Inherit Metab Dis       Date:  1998-02       Impact factor: 4.982

4.  Glycolipid analysis of different tissues and cerebrospinal fluid in type II Gaucher disease.

Authors:  R Gornati; B Berra; G Montorfano; C Martini; G Ciana; P Ferrari; M Romano; B Bembi
Journal:  J Inherit Metab Dis       Date:  2002-02       Impact factor: 4.982

Review 5.  A severity scoring tool to assess the neurological features of neuronopathic Gaucher disease.

Authors:  E H Davies; R Surtees; C DeVile; I Schoon; A Vellodi
Journal:  J Inherit Metab Dis       Date:  2007-09-16       Impact factor: 4.982

6.  Potential efficacy of enzyme replacement and substrate reduction therapy in three siblings with Gaucher disease type III.

Authors:  J Cox-Brinkman; M J van Breemen; B T van Maldegem; L Bour; W E Donker; C E M Hollak; F A Wijburg; J M F G Aerts
Journal:  J Inherit Metab Dis       Date:  2008-10-15       Impact factor: 4.982

7.  Assessment of Basal Metabolic Rate and Nutritional Status in Patients with Gaucher Disease Type III.

Authors:  Divair Doneda; Filippo P Vairo; André L Lopes; Alvaro Reischak-Oliveira; Pedro Schestatsky; Marino M Bianchin; Cileide C Moulin; Ida V D Schwartz
Journal:  JIMD Rep       Date:  2013-12-17

Review 8.  New therapeutic options for lysosomal storage disorders: enzyme replacement, small molecules and gene therapy.

Authors:  Michael Beck
Journal:  Hum Genet       Date:  2006-11-07       Impact factor: 5.881

9.  Previously unrecognized behavioral phenotype in Gaucher disease type 3.

Authors:  Magy Abdelwahab; Michael Potegal; Elsa G Shapiro; Igor Nestrasil
Journal:  Neurol Genet       Date:  2017-05-23
  9 in total

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