Literature DB >> 11758672

Remaining problems in the management of patients with Gaucher disease.

A Erikson1.   

Abstract

The history of treatment of Gaucher disease started with splenectomy and continued with bone marrow transplantation, before the recent introduction of enzyme replacement therapy. Although the latter has revolutionized the prognosis of patients, many questions remain to be answered and clinical management problems resolved. These include how to monitor enzyme replacement to determine the optimal dosage, how to treat mild disease, whether intermittent treatment is an option, and the causes of the neurological signs and how to treat them. The pulmonary hypertension problem has also not been resolved, and we need to determine how to treat and monitor bone disease. In addition, the future role of substrate deprivation needs to be determined, and further research is required before gene therapy becomes a potential clinical option. The high cost of enzyme replacement treatment for Gaucher disease remains an important issue.

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Year:  2001        PMID: 11758672     DOI: 10.1023/a:1012452715079

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  23 in total

1.  Effect of low-dose enzyme replacement therapy on bones in Gaucher disease patients with severe skeletal involvement.

Authors:  D Elstein; I Hadas-Halpern; M Itzchaki; A Lahad; A Abrahamov; A Zimran
Journal:  Blood Cells Mol Dis       Date:  1996       Impact factor: 3.039

2.  Novel oral treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis.

Authors:  T Cox; R Lachmann; C Hollak; J Aerts; S van Weely; M Hrebícek; F Platt; T Butters; R Dwek; C Moyses; I Gow; D Elstein; A Zimran
Journal:  Lancet       Date:  2000-04-29       Impact factor: 79.321

3.  Glucocerebrosidase treatment of type I Gaucher disease with severe pulmonary involvement.

Authors:  M Pelini; D Boice; K O'Neil; J LaRocque
Journal:  Ann Intern Med       Date:  1994-08-01       Impact factor: 25.391

4.  Withdrawal of enzyme replacement therapy in Gaucher's disease.

Authors:  D Elstein; A Abrahamov; I Hadas-Halpern; A Zimran
Journal:  Br J Haematol       Date:  2000-08       Impact factor: 6.998

5.  Prospective study of neurological responses to treatment with macrophage-targeted glucocerebrosidase in patients with type 3 Gaucher's disease.

Authors:  R Schiffmann; M P Heyes; J M Aerts; J M Dambrosia; M C Patterson; T DeGraba; C C Parker; G C Zirzow; K Oliver; G Tedeschi; R O Brady; N W Barton
Journal:  Ann Neurol       Date:  1997-10       Impact factor: 10.422

Review 6.  Enzyme replacement therapy for Gaucher's disease.

Authors:  E Beutler
Journal:  Baillieres Clin Haematol       Date:  1997-12

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

Authors:  N W Barton; R O Brady; J M Dambrosia; A M Di Bisceglie; S H Doppelt; S C Hill; H J Mankin; G J Murray; R I Parker; C E Argoff
Journal:  N Engl J Med       Date:  1991-05-23       Impact factor: 91.245

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

Authors:  A Erikson; M Aström; J E Månsson
Journal:  Neuropediatrics       Date:  1995-08       Impact factor: 1.947

9.  Gaucher disease--Norrbottnian type (III). Neuropaediatric and neurobiological aspects of clinical patterns and treatment.

Authors:  A Erikson
Journal:  Acta Paediatr Scand Suppl       Date:  1986

10.  Aminohydroxy propylidene bisphosphonate (APD) treatment improves the clinical skeletal manifestations of Gaucher's disease.

Authors:  R Samuel; K Katz; S E Papapoulos; Z Yosipovitch; R Zaizov; U A Liberman
Journal:  Pediatrics       Date:  1994-09       Impact factor: 7.124

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  7 in total

Review 1.  Revised recommendations for the management of Gaucher disease in children.

Authors:  Paige Kaplan; Hagit Baris; Linda De Meirleir; Maja Di Rocco; Amal El-Beshlawy; Martina Huemer; Ana Maria Martins; Ioana Nascu; Marianne Rohrbach; Lynne Steinbach; Ian J Cohen
Journal:  Eur J Pediatr       Date:  2012-07-08       Impact factor: 3.183

2.  Substrate reduction therapy of glycosphingolipid storage disorders.

Authors:  Johannes M F G Aerts; Carla E M Hollak; Rolf G Boot; Johanna E M Groener; Mario Maas
Journal:  J Inherit Metab Dis       Date:  2006 Apr-Jun       Impact factor: 4.982

Review 3.  Paediatric non-neuronopathic Gaucher disease: recommendations for treatment and monitoring.

Authors:  Antonio Baldellou; Generoso Andria; Pauline E Campbell; Joel Charrow; Ian J Cohen; Gregory A Grabowski; Chris M Harris; Paige Kaplan; Kieran McHugh; Eugen Mengel; Ashok Vellodi
Journal:  Eur J Pediatr       Date:  2003-12-16       Impact factor: 3.183

Review 4.  Manganese neurotoxicity and the role of reactive oxygen species.

Authors:  Ebany J Martinez-Finley; Claire E Gavin; Michael Aschner; Thomas E Gunter
Journal:  Free Radic Biol Med       Date:  2013-02-08       Impact factor: 7.376

Review 5.  Glucocerebrosidase is shaking up the synucleinopathies.

Authors:  Marina Siebert; Ellen Sidransky; Wendy Westbroek
Journal:  Brain       Date:  2014-02-14       Impact factor: 13.501

Review 6.  Biochemistry of glycosphingolipid storage disorders: implications for therapeutic intervention.

Authors:  Johannes M Aerts; Carla Hollak; Rolf Boot; Ans Groener
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2003-05-29       Impact factor: 6.237

7.  Gaucher disease: clinical profile and therapeutic developments.

Authors:  Timothy M Cox
Journal:  Biologics       Date:  2010-12-06
  7 in total

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