Plexiform neurofibroma in the ear canal of a patient with Type I Neurofibromatosis

por Geller, Mauro, Junior, Luiz Guilherme Darrigo, Filho, Aguinaldo Bonalumi, Ribeiro, Marcia Goncalves
Publicado 2015

Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular char...

por Souza, Josiane, Faucz, Fábio, Sotomaior, Vanessa, Filho, Aguinaldo Bonalumi, Rosenfeld, Jill, Raskin, Salmo
Publicado 2011

Epidemiological profile and clinical characteristics of 491 Brazilian patients with neurofibromatosis type 1

por Darrigo Junior, Luiz Guilherme, Ferraz, Victor Evangelista de Faria, Cormedi, Marina Candido Visontai, Araujo, Luissa Hikari Hayashi, Magalhães, Mariana Prado Silva, Carneiro, Rafaella Curis, Sales, Luis Henrique Nunes, Suchmacher, Mendel, Cunha, Karin Soares, Filho, Aguinaldo Bonalumi, Azulay, David Rubem, Geller, Mauro
Publicado 2022