Proteus syndrome: Clinical diagnosis of a series of cases

por Alves, Cresio, Acosta, Angelina X., Toralles, Maria Betânia P.
Publicado 2013

Association of type 1 diabetes mellitus and autoimmune disorders in Brazilian children and adolescents

por Alves, Crésio, Santos, Larissa Siqueira, Toralles, Maria Betânia P.
Publicado 2016

Interstitial 14q24.3 to q31.3 deletion in a 6-year-old boy with a non-specific dysmorphic phenotype

por Riegel, Mariluce, Moreira, Lilia MA, Espirito Santo, Layla D, Toralles, Maria Betânia P, Schinzel, Albert
Publicado 2014

Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report

por Alves, Rita Maria, Uva, Paolo, Veiga, Marielza F., Oppo, Manuela, Zschaber, Fabiana C. R., Porcu, Giampiero, Porto, Henrique P., Persico, Ivana, Onano, Stefano, Cuccuru, Gianmauro, Atzeni, Rossano, Vieira, Lauro C. N., Pires, Marcos V. A., Cucca, Francesco, Toralles, Maria Betânia P., Angius, Andrea, Crisponi, Laura
Publicado 2019