APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal segmental glomerulosclerosis and other diagnoses von Watanabe, Andreia, Guaragna, Mara Sanches, Belangero, Vera Maria Santoro, Casimiro, Fernanda Maria Serafim, Pesquero, João Bosco, de Santis Feltran, Luciana, Palma, Lilian Monteiro Pereira, Varela, Patrícia, de Menezes Neves, Precil Diego Miranda, Lerario, Antonio Marcondes, de Souza, Marcela Lopes, de Mello, Maricilda Palandi, de Brito Lutaif, Anna Cristina Gervásio, Ferrari, Cassio Rodrigues, Sampson, Matthew Gordon, Onuchic, Luiz Fernando, Nogueira, Paulo Cesar Koch

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Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study von Riccetto, Luísa, Vieira, Tarsis Paiva, Viguetti-Campos, Nilma Lucia, Mazzola, Tais Nitsch, Guaragna, Mara Sanches, Fabbri-Scallet, Helena, Mello, Maricilda Palandi de, Marques-de-Faria, Antonia Paula, Maciel-Guerra, Andrea Trevas, Guerra Junior, Gil

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Leydig and Sertoli cell function in individuals with genital ambiguity, 46,XY karyotype, palpable gonads and normal testosterone secretion: a case-control study von Guaragna-Filho, Guilherme, Calixto, Antônio Ramos, Astur, Anna Beatriz Lima do Valle, Paula, Georgette Beatriz de, Oliveira, Laurione Cândido de, Morcillo, André Moreno, Gonçalves, Ezequiel Moreira, Mello, Maricilda Palandi de, Maciel-Guerra, Andrea Trevas, Guerra-Junior, Gil

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Mutation update for the NR5A1 gene involved in DSD and infertility von Fabbri‐Scallet, Helena, Sousa, Lizandra Maia, Maciel‐Guerra, Andréa Trevas, Guerra‐Júnior, Gil, Mello, Maricilda Palandi

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Complete gonadal dysgenesis in clinical practice: the 46,XY karyotype accounts for more than one third of cases von Rocha, Vanessa Brito Campoy, Guerra-Júnior, Gil, M.D., Ph.D, Marques-de-Faria, Antonia Paula, M.D., Ph.D, de Mello, Maricilda Palandi, Ph.D, Maciel-Guerra, Andréa Trevas, M.D., Ph.D

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Prenatal Findings in Postnatal Cases of Disorders of Sex Development: Experience from a Tertiary-Specialized Center in Brazil von Cursino, Kleber Andrade, Garcia, Guilherme Mantelato, Barros, Beatriz Amstalden, Mazzola, Tais Nitsch, Fabbri-Scallet, Helena, Guaragna, Mara Sanches, Vieira, Tarsis Antonio Paiva, Mello, Maricilda Palandi de, Maciel-Guerra, Andrea Trevas, Guerra-Junior, Gil

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X‐linked congenital adrenal hypoplasia: Report of long clinical follow‐up and description of a new complex variant in the NR0B1 gene von Esquiaveto‐Aun, Adriana Mangue, Mello, Maricilda Palandi, Guaragna, Mara Sanches, Silva Lopes, Vera Lúcia Gil, Francese‐Santos, Ana Paula, Santos Cruz Piveta, Cristiane, Mazolla, Taís Nitsh, Lemos‐Marini, Sofia Helena Valente, Guerra‐Junior, Gil

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SOX3 duplication in a boy with 46,XX ovotesticular disorder of sex development and his 46,XX sister with atypical genitalia: Probable germline mosaicism von Oliveira, Flávia Marcorin, Barros, Beatriz Amstalden, Santos, Ana Paula, Campos, Nilma Lúcia Viguetti, Mazzola, Taís Nitsch, Filho, Paulo Latuf, Andrade, Liliana Aparecida Lucci De Angelo, Guaragna, Mara Sanches, Mello, Maricilda Palandi, Guerra‐Junior, Gil, Vieira, Társis Antonio Paiva, Maciel‐Guerra, Andréa Trevas

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Are NR5A1 Variations a Frequent Cause of 46,XX Ovotesticular Disorders of Sex Development? Analysis from a Single Center and Systematic Review von Barros, Beatriz Amstalden, Guaragna, Mara Sanches, Fabbri-Scallet, Helena, Palandi de Mello, Maricilda, Guerra-Júnior, Gil, Maciel-Guerra, Andréa Trevas

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A study of splicing mutations in disorders of sex development von de Calais, Flavia Leme, Smith, Lindsay D., Raponi, Michela, Maciel-Guerra, Andréa Trevas, Guerra-Junior, Gil, de Mello, Maricilda Palandi, Baralle, Diana

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Prevalence of Testicular Adrenal Rest Tumor and Factors Associated with Its Development in Congenital Adrenal Hyperplasia von Mendes-dos-Santos, Carolina Taddeo, Martins, Daniel Lahan, Guerra-Júnior, Gil, Baptista, Maria Tereza Matias, de-Mello, Maricilda Palandi, de Oliveira, Laurione Candido, Morcillo, André Moreno, Lemos-Marini, Sofia Helena Valente

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Insights from a Wolfram syndrome cohort: clinical and molecular findings from a specialized diabetes reference center von Lopes, Carolina Paniago, Gonçalves, Gentil Ferreira, Paulino, Maria Fernanda Vanti Macedo, Esquiaveto-Aun, Adriana Mangue, de Mello, Maricilda Palandi, Pavin, Elizabeth João, Breder, Ikaro Soares Santos, Pu, Mariana Zorron Mei Hsia, de Lemos-Marini, Sofia Helena Valente, Guerra, Gil

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Promises and pitfalls of whole-exome sequencing exemplified by a nephrotic syndrome family von Guaragna, Mara Sanches, de Brito Lutaif, Anna Cristina Gervásio, de Souza, Marcela Lopes, Maciel-Guerra, Andréa Trevas, Belangero, Vera Maria Santoro, Guerra-Júnior, Gil, de Mello, Maricilda Palandi

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DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis von de Oliveira, Felipe Rodrigues, Mazzola, Taís Nitsch, de Mello, Maricilda Palandi, Francese-Santos, Ana Paula, Lemos-Marini, Sofia Helena V de, Maciel-Guerra, Andrea Trevas, Hiort, Olaf, Werner, Ralf, Guerra-Junior, Gil, Fabbri-Scallet, Helena

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Accuracy of anthropometric measurements in estimating fat mass in individuals with 21-hydroxylase deficiency von Gonçalves, Ezequiel Moreira, M.Sc, Silva, Analiza M., Ph.D, Santos, Diana A., B.Sc, Lemos-Marini, Sofia Helena Valente, Ph.D, de Oliveira Santos, Allan, Ph.D, Mendes-dos-Santos, Carolina Taddeo, M.D, De-Mello, Maricilda Palandi, Ph.D, Guerra-Júnior, Gil, Ph.D

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Molecular diagnosis of 5α-reductase type II deficiency in Brazilian siblings with 46,XY disorder of sex development von Leme 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

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So, and if it is not congenital adrenal hyperplasia? Addressing an undiagnosed case of genital ambiguity von de Omena Filho, Reinaldo Luna, Petroli, Reginaldo José, Soardi, Fernanda Caroline, de Paula Michelatto, Débora, Mazzola, Taís Nitsch, Fabbri-Scallet, Helena, de Mello, Maricilda Palandi, Zanotti, Susane Vasconcelos, Gubert, Ida Cristina, Monlleo, Isabella

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Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia von Karlsson, Leif, de Paula Michelatto, Débora, Lusa, Ana Letícia Gori, D'Almeida Mgnani Silva, Camila, Östberg, Linus J., Persson, Bengt, Guerra-Júnior, Gil, Valente de Lemos-Marini, Sofia Helena, Baldazzi, Lilia, Menabó, Soara, Balsamo, Antonio, Greggio, Nella Augusta, Palandi de Mello, Maricilda, Barbaro, Michela, Lajic, Svetlana

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Dopamine D2 receptor gene polymorphisms and externalizing behaviors in children and adolescents von Della Torre, Osmar Henrique, Paes, Lúcia Arisaka, Henriques, Taciane Barbosa, de Mello, Maricilda Palandi, Celeri, Eloisa Helena Rubello Valler, Dalgalarrondo, Paulo, Guerra-Júnior, Gil, Santos-Júnior, Amilton Dos

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Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a cross-sectional study of factors involved in bone mineral density von OLIVEIRA DE ALMEIDA FREIRE, Patricia, VALENTE DE LEMOS-MARINI, Sofia Helena, TREVAS MACIEL-GUERRA, Andréa, MORENO MORCILLO, André, MATIAS BAPTISTA, Maria Tereza, PALANDI DE MELLO, Maricilda, GUERRA, Gil JR

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