Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity
Margutti, Ana Vitoria Barban, Silva, Wilson Araújo, Garcia, Daniel Fantozzi, de Molfetta, Greice Andreotti, Marques, Adriana Aparecida, Amorim, Tatiana, Prazeres, Vânia Mesquita Gadelha, Boy da Silva, Raquel Tavares, Miura, Irene Kazue, Seda Neto, João, Santos, Emerson de Santana, Santos, Mara Lúcia Schmitz Ferreira, Lourenço, Charles Marques, Tonon, Tássia, Sperb-Ludwig, Fernanda, de Souza, Carolina Fischinger Moura, Schwartz, Ida Vanessa Döederlein, Camelo, José Simon
Published in Orphanet journal of rare diseases (01.11.2020)
Published in Orphanet journal of rare diseases (01.11.2020)
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Assessment of the tongue frenulum in Beckwith-Wiedemann syndrome: Pre- and post-frenectomy findings
César, Carla Patrícia Hernandez Alves Ribeiro, Torres, Geciane Maria Xavier, Andrade, Natália Silva, Vanderlei, Katharina Morant Holanda de Oliveira, Nascimento, Karla Monique de Souza, Barroso, Brenna Geovania Izaura Santos, Santos, Emerson de Santana
Published in Special care in dentistry (01.07.2021)
Published in Special care in dentistry (01.07.2021)
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Clinical orofacial and myofunctional manifestations in an adolescent with Noonan Syndrome: a case report
Torres, Geciane Xavier, Santos, Emerson de Santana, Cesar, Carla Patricia Hernandez Alves Ribeiro, Irineu, Roxane de Alencar, Dias, Isabel Ribeiro Rocha, Ramos, Alice Fontes
Published in Revista CEFAC (01.07.2020)
Published in Revista CEFAC (01.07.2020)
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Journal Article
Maple Syrup Urine Disease in Brazilian Patients: Variants and Clinical Phenotype Heterogeneity
Ana Vitoria Barban Margutti, Wilson Araújo Silva, Daniel Fantozzi Garcia, Greice Andreotti de Molfetta, Adriana Aparecida Marques, Amorim, Tatiana, Vânia Mesquita Gadelha Prazeres, Raquel Tavares Boy da Silva, Irene Kazue Miura, João Seda Neto, de Santana Santos, Emerson, Mara Lúcia Schmitz Ferreira Santos, Charles Marques Lourenço, Tonon, Tássia, Sperb-Ludwig, Fernanda, Carolina Fischinger Moura de Souza, Ida Vanessa Döederlein Schwartz, José Simon Camelo Junior
Published in Orphanet Journal of Rare Diseases (20.10.2020)
Published in Orphanet Journal of Rare Diseases (20.10.2020)
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