Enzyme replacement therapy for Fabry disease: A systematic review and meta-analysis

Por Alegra, Taciane, Vairo, Filippo, de Souza, Monica V., Krug, Bárbara C., Schwartz, Ida V.D.
Publicado em 2012

A de novo or germline mutation in a family with Mucolipidosis III gamma: Implications for molecular diagnosis and genetic counseling

Por Velho, Renata Voltolini, Alegra, Taciane, Sperb, Fernanda, Ludwig, Nataniel Floriano, Saraiva-Pereira, Maria Luiza, Matte, Ursula, Schwartz, Ida V.D.
Publicado no Mol Genet Metab Rep (2014)

Quality of Life of Brazilian Patients with Gaucher Disease and Fabry Disease

Por Oliveira, Fabiane Lopes, Alegra, Taciane, Dornelles, Alicia, Krug, Bárbara Corrêa, Netto, Cristina B. O., da Rocha, Neusa Sica, Picon, Paulo D., Schwartz, Ida Vanessa D.
Publicado em 2012

Pitfalls in the prenatal diagnosis of mucolipidosis II alpha/beta: A case report

Por Alegra, Taciane, Koppe, Tiago, Acosta, Angelina, Sarno, Manoel, Burin, Maira, Kessler, Rejane Gus, Sperb-Ludwig, Fernanda, Cury, Gabriela, Baldo, Guilherme, Matte, Ursula, Giugliani, Roberto, Schwartz, Ida Vanessa D.
Publicado no Meta Gene (2014)