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Page 1
Guidelines for the management of mucopolysaccharidosis type I.
Martins AM, Dualibi AP, Norato D, Takata ET, Santos ES, Valadares ER, Porta G, de Luca G, Moreira G, Pimentel H, Coelho J, Brum JM, Semionato Filho J, Kerstenetzky MS, Guimarães MR, Rojas MV, Aranda PC, Pires RF, Faria RG, Mota RM, Matte U, Guedes ZC. Martins AM, et al. Among authors: pires rf. J Pediatr. 2009 Oct;155(4 Suppl):S32-46. doi: 10.1016/j.jpeds.2009.07.005. J Pediatr. 2009. PMID: 19765409 Review. No abstract available.
Recommendations on diagnosis, treatment, and monitoring for Gaucher disease.
Martins AM, Valadares ER, Porta G, Coelho J, Semionato Filho J, Pianovski MA, Kerstenetzky MS, Montoril Mde F, Aranda PC, Pires RF, Mota RM, Bortolheiro TC; Brazilian Study Group on Gaucher Disease and other Lysosomal Storage Diseases. Martins AM, et al. Among authors: pires rf. J Pediatr. 2009 Oct;155(4 Suppl):S10-8. doi: 10.1016/j.jpeds.2009.07.004. J Pediatr. 2009. PMID: 19765407 Review. No abstract available.
Comparison between the biochemical properties of plasma chitotriosidase from normal individuals and from patients with Gaucher disease, GM1-gangliosidosis, Krabbe disease and heterozygotes for Gaucher disease.
Wajner A, Michelin K, Burin MG, Pires RF, Pereira ML, Giugliani R, Coelho JC. Wajner A, et al. Among authors: pires rf. Clin Biochem. 2007 Mar;40(5-6):365-9. doi: 10.1016/j.clinbiochem.2006.12.003. Epub 2007 Jan 8. Clin Biochem. 2007. PMID: 17291472
51 results