Research article summary (published 29 Sep 2009):

Recommendations on diagnosis, treatment, and monitoring for Gaucher disease.

Full Abstract

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Author information

Author/s: Martins, Ana Maria (AM); Valadares, Eugenia Ribeiro (ER); Porta, Gilda (G); Coelho, Janice (J); Semionato Filho, José (J); Pianovski, Mara Albonei Dudeque (MA); Kerstenetzky, Marcelo Soares (MS); Montoril, Maria de Fátima Pombo (Mde F); Aranda, Paulo Cesar (PC); Pires, Ricardo Flores (RF); Mota, Ronald Moura Vale (RM); Bortolheiro, Teresa Cristina (TC); Brazilian Study Group on Gaucher Disease and other Lysosomal Storage Diseases;

Affiliation: Centro de Referência em Erros Inatos, Universidade Federal de São Paulo, São Paulo, Brazil. anamartins.dped(-atsign-)epm.br

Journal and publication information

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review

Journal: The Journal of pediatrics (J Pediatr), published in United States. (Language: eng)

Reference: 2009-Oct; vol 155 (issue 4 Suppl) : pp S10-8

Dates: Created 2009/09/21; Completed 2009/10/22;

PMID: 19765407, status: MEDLINE (last retrieval date: 10/22/2009, IMS Date: )

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Brazil Gaucher Disease - complications; diagnosis; therapy Glucosylceramidase - therapeutic use Humans

Humans Patient Selection Practice Guidelines as Topic Risk Assessment

Associated Chemicals: imiglucerase (EC 3.2.1.-) ; Glucosylceramidase (EC 3.2.1.45)

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