Maricilda Palandi de Mello
Universidade Estadual de Campinas
H-index: 30
Latin America-Brazil
Top articles of Maricilda Palandi de Mello
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
X‐linked congenital adrenal hypoplasia: Report of long clinical follow‐up and description of a new complex variant in the NR0B1 gene | American Journal of Medical Genetics Part A | Adriana Mangue Esquiaveto‐Aun Maricilda Palandi de Mello Mara Sanches Guaragna Vera Lúcia Gil da Silva Lopes Ana Paula Francese‐Santos | 2024/1/19 |
Prenatal Findings in Postnatal Cases of Disorders of Sex Development: Experience from a Tertiary-Specialized Center in Brazil | Fetal Diagnosis and Therapy | Kleber Andrade Cursino Guilherme Mantelato Garcia Beatriz Amstalden Barros Tais Nitsch Mazzola Helena Fabbri-Scallet | 2024/1/4 |
DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis | Life | Felipe Rodrigues de Oliveira Taís Nitsch Mazzola Maricilda Palandi de Mello Ana Paula Francese-Santos Sofia Helena V de Lemos-Marini | 2023/4/27 |
Are NR5A1 Variations a Frequent Cause of 46,XX Ovotesticular Disorders of Sex Development? Analysis from a Single Center and Systematic Review | Beatriz Amstalden Barros Mara Sanches Guaragna Helena Fabbri-Scallet Maricilda Palandi de Mello Gil Guerra-Júnior | 2023/2/14 | |
SOX3 duplication in a boy with 46,XX ovotesticular disorder of sex development and his 46,XX sister with atypical genitalia: Probable germline mosaicism | American Journal of Medical Genetics Part A | Flávia Marcorin de Oliveira Beatriz Amstalden Barros Ana Paula Dos Santos Nilma Lúcia Viguetti Campos Taís Nitsch Mazzola | 2023/2 |
Diferenciação sexual diferente | Leandra STEINMETZ Durval DAMIANI Maricilda Palandi de MELLO Pedro Saddi ROSA José Viana LIMA JUNIOR | 2023 | |
DHX37 and the implications in Disorders of Sex Development: an update review. | Felipe Rodrigues de Oliveira Mara Sanches Guaragna Andréa Trevas Maciel-Guerra Beatriz Amstalden Barros Maricilda Palandi de Mello | 2023/12/23 | |
Bilateral Wilms’ tumor in a child with Denys-Drash syndrome: novel frameshift variant disrupts the WT1 nuclear location signaling region | Journal of Pediatric Endocrinology and Metabolism | Mara Sanches Guaragna Felipe Lourenço Ledesma Victoria Zavanelli Manzano Andréa Trevas Maciel-Guerra Gil Guerra-Júnior | 2022/6/27 |
Can non-coding NR5A1 gene variants explain phenotypes of disorders of sex development? | Sexual Development | Helena Fabbri-Scallet Ralf Werner Mara S Guaragna Juliana GR de Andrade Andrea T Maciel-Guerra | 2022/12/28 |
So, and if it is not congenital adrenal hyperplasia? Addressing an undiagnosed case of genital ambiguity | Italian Journal of Pediatrics | Reinaldo Luna de Omena Filho Reginaldo José Petroli Fernanda Caroline Soardi Débora de Paula Michelatto Taís Nitsch Mazzola | 2022/6/10 |
Trends in Time Regarding Sex Assignment of Patients with Disorders of Sex Development: Experience of an Interdisciplinary Service | Sexual Development | Julia P Vicentin Mayra de Souza El Beck Carlos W Germano Juliana GR Andrade Beatriz A Barros | 2022/12/28 |
Leydig and Sertoli cell function in individuals with genital ambiguity, 46, XY karyotype, palpable gonads and normal testosterone secretion: a case-control study | Sao Paulo Medical Journal | Guilherme Guaragna-Filho Antônio Ramos Calixto Anna Beatriz Lima do Valle Astur Georgette Beatriz de Paula Laurione Cândido de Oliveira | 2022/2/7 |
Suggested cutoff point for testosterone by liquid chromatography with tandem mass spectrometry (LC-MS/MS) after stimulation with recombinant human chorionic gonadotropin | Sexual Development | Leticia R de Oliveira Carlos A Longui Guilherme Guaragna-Filho José L da Costa Rafael Lanaro | 2022/12/28 |
Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study | Sao Paulo Medical Journal | Luísa Riccetto Tarsis Paiva Vieira Nilma Lucia Viguetti-Campos Tais Nitsch Mazzola Mara Sanches Guaragna | 2022/11/28 |
Sex dimorphism of weight and length at birth: evidence based on disorders of sex development | Annals of human biology | DSR Amais TER da Silva BA Barros JGR de Andrade SHV de Lemos-Marini | 2022/11/17 |
A Novel Look at Dosage-Sensitive Sex Locus Xp21.2 in a Case of 46,XY Partial Gonadal Dysgenesis without NR0B1 Duplication | International Journal of Molecular Sciences | Ana Paula Francese-Santos Jakob A Meinel Cristiane SC Piveta Juliana GR Andrade Beatriz A Barros | 2022/12/28 |
P0267/# 595: ASSOCIATION BETWEEN APPARENT STRONG ION DIFFERENCE (SIDAPP) AND OUTCOMES IN TERTIARY PEDIATRIC INTENSIVE CARE UNIT (PICU) FROM BRAZILIAN AMAZON: AN OBSERVATIONAL STUDY | Pediatric Critical Care Medicine | E Farias C Costa M Mello A Leão | 2021/3/1 |
APOL1 in an ethnically diverse pediatric population with nephrotic syndrome: implications in focal segmental glomerulosclerosis and other diagnoses | Pediatric Nephrology | Andreia Watanabe Mara Sanches Guaragna Vera Maria Santoro Belangero Fernanda Maria Serafim Casimiro João Bosco Pesquero | 2021/8 |
Association between Down Syndrome and Disorders of Sex Development: Report of Three Cases and Review of 188 Cases in the Literature | Sexual Development | Octavio O Santos-Neto Marina H Mariano Antonia P Marques-de-Faria Juliana GR Andrade Tarsis AP Vieira | 2021/7/30 |
Sex Dimorphism of Birth Weight and Length: Evidence Based on Disorders of Sex Development | Debora Stabile Romero Amais Tainara Emilia Rodrigues da Silva Beatriz Amstalden Barros Juliana Gabriel Ribeiro de Andrade Sofia Helena Valente de Lemos-Marini | 2021/5/17 |
Co-Authors
