Neurological evaluation of microcephalic children with Zika syndrome and congenital cytomegalovirus infection

por Faccini, Lavinia Schüler, Friedrich, Luciana, de Moura, Sara Kvitko, Maria, Fernanda Diffini Santa, da Silva Inácio de Bone, Steice
Publicado 2022

Polymorphisms and genetic susceptibility of type 1 diabetes mellitus and celiac disease

por Bastos, Marília Dornelles, Kowalski, Thayne Woycinck, Mariath, Luiza Monteavaro, Puñales, Marcia Khaled, Tscheidel, Balduíno, de Godoy, Bibiane Armiliato, Coutinho, Lara Dias, Mundstock, Rafaela Fernandes, Faccini, Lavínia Schüler, da Silveira, Themis Reverbel
Publicado 2015

Haplotype analysis of DQ2.5 and DQ8 by simple nucleotide polymorphism technique (TAG-SNP) in type 1 diabetes and/or celiac disease patients

por Bastos, Marília Dornelles, Kowalski, Thayne Woycinck, Mariath, Luiza Monteavaro, Puñales, Márcia Khaled, Tschiedel, Balduíno, da Silva, Ana Carolina Moisés, Tavares, Maria Eduarda, Pires, Ana Luiza Guedes, Faccini, Lavínia Schüler, da Silveira, Themis Reverbel
Publicado 2015

Information and Diagnosis Networks – tools to improve diagnosis and treatment for patients with rare genetic diseases

por Vieira, Taiane Alves, Trapp, Franciele Barbosa, de Souza, Carolina Fischinger Moura, Faccini, Lavínia Schuler, Jardim, Laura Bannach, Schwartz, Ida Vanessa Doederlein, Riegel, Mariluce, Vargas, Carmen Regla, Burin, Maira Graeff, Leistner-Segal, Sandra, Ashton-Prolla, Patrícia, Giugliani, Roberto
Publicado 2019