Research article summary (published 29 Sep 2009):

Guidelines to diagnosis and monitoring of Fabry disease and review of treatment experiences.

Full Abstract

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Author information

Author/s: Martins, Ana Maria (AM); D'Almeida, Vânia (V); Kyosen, Sandra Obikawa (SO); Takata, Edna Tiemi (ET); Delgado, Alvimar Gonçalves (AG); Gonçalves, Angela Maria Barbosa Ferreira (AM); Benetti Filho, Caio César (CC); Martini Filho, Dino (D); Biagini, Gilson (G); Pimentel, Helena (H); Abensur, Hugo (H); Guimarães, Humberto Cenci (HC); Gomes, Jaelson Guilhem (JG); Sobral Neto, José (J); D'Almeida, Luiz Octávio Dias (LO); Carvalho, Luiz Roberto (LR); Harouche, Maria Beatriz (MB); Maldonado, Maria Cristina Jacometti (MC); Nascimento, Osvaldo J M (OJ); Montoril, Paulo Sergio dos Santos (PS); Bastos, Ricardo Villela (RV);

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

Journal and publication information

Publication Type: Journal Article; Review

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

Reference: 2009-Oct; vol 155 (issue 4 Suppl) : pp S19-31

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

PMID: 19765408, 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.

Adult Age Factors Brazil Cohort Studies Fabry Disease - diagnosis; etiology; therapy Female Genetic Predisposition to Disease

Genetic Predisposition to Disease Humans Male Practice Guidelines as Topic Sex Factors Treatment Outcome alpha-Galactosidase - genetics; metabolism

Associated Chemicals: alpha-Galactosidase (EC 3.2.1.22)

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