Your search returned 3 results.

Results
	1.	Satoyoshi syndrome in a Caucasian girl improved with glucocorticoids--a clinical report. [electronic resource] by Cecchin, Cláudia Rafaela Félix, Têmis Maria Magalhães, Richard B Furlanetto, Tânia Weber Producer: 20031023 In: American journal of medical genetics. Part A vol. 118A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Kidney function and 24-hour proteinuria in patients with Fabry disease during 36 months of agalsidase alfa enzyme replacement therapy: a Brazilian experience. [electronic resource] by Thofehrn, Scheila Netto, Cristina Cecchin, Cláudia Burin, Maira Matte, Ursula Brustolin, Sílvia Nunes, Ane Cláudia Fernandes Coelho, Janice Tsao, Marylin Jardim, Laura Giugliani, Roberto Barros, Elvino José Guardão Producer: 20100406 In: Renal failure vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	White matter lesions in Fabry disease before and after enzyme replacement therapy: a 2-year follow-up. [electronic resource] by Jardim, Laura B Aesse, Flávio Vedolin, Leonardo M Pitta-Pinheiro, Cláudio Marconato, João Burin, Maira G Cecchin, Cláudia Netto, Cristina B O Matte, Ursula S Pereira, Fernanda Kalakun, Luciane Giugliani, Roberto Producer: 20070405 In: Arquivos de neuro-psiquiatria vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)