Menino ou Menina ? : distúrbios da diferenciação do sexo /

per Maciel-Guerra, Andréa Trevas, Guerra-Junior, Gil
Publicat 2010.

FSH may be a useful tool to allow early diagnosis of Turner syndrome

per Carpini, Stela, Carvalho, Annelise Barreto, de Lemos-Marini, Sofia Helena Valente, Guerra-Junior, Gil, Maciel-Guerra, Andréa Trevas
Publicat a BMC Endocr Disord (2018)

Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy

per Amaral-Fernandes, Marcela Scabello, Marcondes, Ana Maria, Miranda, Paulo Maurício do Amor Divino, Maciel-Guerra, Andréa Trevas, Sartorato, Edi Lúcia
Publicat 2011

Optimization of a genotyping screening based on hydrolysis probes to detect the main mutations related to Leber hereditary optic neuropathy (LHON)

per Martins, Fábio Tadeu Arrojo, Miranda, Paulo Maurício do Amor Divino, Fernandes, Marcela Scabello Amaral, Maciel-Guerra, Andréa Trevas, Sartorato, Edi Lúcia
Publicat a Mol Vis (2017)

A study of splicing mutations in disorders of sex development

per de Calais, Flavia Leme, Smith, Lindsay D., Raponi, Michela, Maciel-Guerra, Andréa Trevas, Guerra-Junior, Gil, de Mello, Maricilda Palandi, Baralle, Diana
Publicat a Sci Rep (2017)

Complete androgen insensitivity syndrome and risk of gonadal malignancy: systematic review

per Barros, Beatriz Amstalden, de Oliveira, Letícia Ribeiro, Surur, Cíntia Regina Crocetti, Barros-Filho, Antonio de Azevedo, Maciel-Guerra, Andrea Trevas, Guerra-Junior, Gil
Publicat a Ann Pediatr Endocrinol Metab (2021)

Long-Term Follow-Up of Patients with 46,XY Partial Gonadal Dysgenesis Reared as Males

per Gabriel Ribeiro de Andrade, Juliana, Marques-de-Faria, Antonia Paula, Fabbri, Helena Campos, de Mello, Maricilda Palandi, Guerra-Júnior, Gil, Maciel-Guerra, Andréa Trevas
Publicat a Int J Endocrinol (2014)

Screening of Y chromosome microdeletions in 46,XY partial gonadal dysgenesis and in patients with a 45,X/46,XY karyotype or its variants

per dos Santos, Ana Paula, Ribeiro Andrade, Juliana Gabriel, Piveta, Cristiane Santos Cruz, de Paulo, Juliana, Guerra-Junior, Gil, de Mello, Maricilda Palandi, Maciel-Guerra, Andréa Trevas
Publicat 2013

The novel p.Cys65Tyr mutation in NR5A1 gene in three 46,XY siblings with normal testosterone levels and their mother with primary ovarian insufficiency

per Fabbri, Helena Campos, de Andrade, Juliana Gabriel Ribeiro, Soardi, Fernanda Caroline, de Calais, Flávia Leme, Petroli, Reginaldo José, Maciel-Guerra, Andréa Trevas, Guerra-Júnior, Gil, de Mello, Maricilda Palandi
Publicat 2014

Molecular Diagnosis of 5α-Reductase Type II Deficiency in Brazilian Siblings with 46,XY Disorder of Sex Development

per de Calais, Flávia Leme, Soardi, Fernanda Caroline, Petroli, Reginaldo José, Lusa, Ana Letícia Gori, de Paiva e Silva, Roberto Benedito, Maciel-Guerra, Andréa Trevas, Guerra-Júnior, Gil, de Mello, Maricilda Palandi
Publicat 2011

SUN-086 Pilot Study Using Aromatase Inhibitor in Puberty of Boys With Partial Androgen Insensitivity: Report of Three Cases

per Maciel-Guerra, Andrea Trevas, de Andrade, Juliana Gabriel Ribeiro, de Souza, Arina Tavares, Campos, Mariana Baldini, Marques-Junior, Hercules Oliveira, Guaragna, Mara Sanches, Fabbri-Scallet, Helena, de Mello, Maricilda Palandi, Guerra-Junior, Gil
Publicat a J Endocr Soc (2020)

MON-056 Rare X Chromosome Pericentric Inversion Associated with Ovotesticular Disorder of Sex Development

per Guerra-Junior, Gil, Santos, Ana Paula, Oliveira, Flavia M, Vieira, Tarsis A P, Campos, Nilma L V, Miranda, Marcio L, Guaragna, Mara S, Fabbri-Scallet, Helena, de Mello, Maricilda P, Maciel-Guerra, Andrea Trevas
Publicat a J Endocr Soc (2020)

Androgens by immunoassay and mass spectrometry in children with 46,XY disorder of sex development

per Oliveira, Letícia Ribeiro, Longui, Carlos Alberto, Guaragna-Filho, Guilherme, Costa, José Luiz, Lanaro, Rafael, Silva, David Antônio, Chiamolera, Maria Izabel, de Mello, Maricilda Palandi, Morcillo, André Moreno, Maciel-Guerra, Andrea Trevas, Guerra-Junior, Gil
Publicat a Endocr Connect (2020)

Clinical and Laboratorial Features That May Differentiate 46,XY DSD due to Partial Androgen Insensitivity and 5α-Reductase Type 2 Deficiency

per Veiga-Junior, Nélio Neves, Medaets, Pedro Augusto Rodrigues, Petroli, Reginaldo José, Calais, Flávia Leme, de Mello, Maricilda Palandi, Castro, Carla Cristina Telles de Sousa, Guaragna-Filho, Guilherme, Sewaybricker, Letícia Espósito, Marques-de-Faria, Antonia Paula, Maciel-Guerra, Andréa Trevas, Guerra-Junior, Gil
Publicat 2012

Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study

per del Castillo, Ignacio, Moreno-Pelayo, Miguel A., del Castillo, Francisco J., Brownstein, Zippora, Marlin, Sandrine, Adina, Quint, Cockburn, David J., Pandya, Arti, Siemering, Kirby R., Chamberlin, G. Parker, Ballana, Ester, Wuyts, Wim, Maciel-Guerra, Andréa Trevas, Álvarez, Araceli, Villamar, Manuela, Shohat, Mordechai, Abeliovich, Dvorah, Dahl, Hans-Henrik M., Estivill, Xavier, Gasparini, Paolo, Hutchin, Tim, Nance, Walter E., Sartorato, Edi L., Smith, Richard J. H., Van Camp, Guy, Avraham, Karen B., Petit, Christine, Moreno, Felipe
Publicat 2003

408 Cases of Genital Ambiguity Followed by Single Multidisciplinary Team during 23 Years: Etiologic Diagnosis and Sex of Rearing

per De Paula, Georgette Beatriz, Barros, Beatriz Amstalden, Carpini, Stela, Tincani, Bruna Jordan, Mazzola, Tais Nitsch, Sanches Guaragna, Mara, Piveta, Cristiane Santos da Cruz, de Oliveira, Laurione Candido, Andrade, Juliana Gabriel Ribeiro, Guaragna-Filho, Guilherme, Barbieri, Pedro Perez, Ferreira, Nathalia Montibeler, Miranda, Marcio Lopes, Gonçalves, Ezequiel Moreira, Morcillo, Andre Moreno, Viguetti-Campos, Nilma Lucia, Lemos-Marini, Sofia Helena Valente, Silva, Roberto Benedito de Paiva, Marques-de-Faria, Antonia Paula, De Mello, Maricilda Palandi, Maciel-Guerra, Andrea Trevas, Guerra-Junior, Gil
Publicat a Int J Endocrinol (2016)