I agree that this site is using cookies. You can find further informations here.
X
de Mello, Maricilda Palandi
88  results:
Search for persons X
?
1

X‐linked congenital adrenal hypoplasia: Report of long clin..:

Esquiaveto‐Aun, Adriana Mangue ; de Mello, Maricilda Palandi ; Guaragna, Mara Sanches...
American Journal of Medical Genetics Part A.  194 (2024)  6 - p. , 2024
Link: https://doi.org/10.1002/..
 
?
2

Clinical and laboratory differences between chromosomal and..:

Riccetto, Luísa ; Vieira, Tarsis Paiva ; Viguetti-Campos, Nilma Lucia...
Sao Paulo Medical Journal.  141 (2023)  4 - p. , 2023
Link: https://doi.org/10.1590/..
 
?
3

DHX37 and NR5A1 Variants Identified in Patients with 46,XY ..:

de Oliveira, Felipe Rodrigues ; Mazzola, Taís Nitsch ; de Mello, Maricilda Palandi...
Life.  13 (2023)  5 - p. 1093 , 2023
Link: https://doi.org/10.3390/..
 
?
4

So, and if it is not congenital adrenal hyperplasia? Addres..:

de Omena Filho, Reinaldo Luna ; Petroli, Reginaldo José ; Soardi, Fernanda Caroline...
Italian Journal of Pediatrics.  48 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
?
5

SOX3 duplication in a boy with 46,XX ovotesticular disorder..:

de Oliveira, Flávia Marcorin ; Barros, Beatriz Amstalden ; dos Santos, Ana Paula...
American Journal of Medical Genetics Part A.  191 (2022)  2 - p. 592-598 , 2022
Link: https://doi.org/10.1002/..
 
?
6

Leydig and Sertoli cell function in individuals with genita..:

Guaragna-Filho, Guilherme ; Calixto, Antônio Ramos ; Astur, Anna Beatriz Lima do Valle...
Sao Paulo Medical Journal.  140 (2022)  2 - p. 163-170 , 2022
Link: https://doi.org/10.1590/..
 
?
7

APOL1 in an ethnically diverse pediatric population with ne..:

Watanabe, Andreia ; Guaragna, Mara Sanches ; Belangero, Vera Maria Santoro...
Pediatric Nephrology.  , 2021
Link: https://doi.org/10.1007/..
 
?
8

SUN-086 Pilot Study Using Aromatase Inhibitor in Puberty of..:

Guerra-Junior, Gil ; de Mello, Maricilda Palandi ; Fabbri-Scallet, Helena...
Journal of the Endocrine Society.  4 (2020)  Supplement_1 - p. , 2020
Link: https://doi.org/10.1210/..
 
?
9

Mutation update for theNR5A1gene involved in DSD and infert..:

Fabbri‐Scallet, Helena ; Sousa, Lizandra Maia ; Maciel‐Guerra, Andréa Trevas..
Human Mutation.  41 (2019)  1 - p. 58-68 , 2019
Link: https://doi.org/10.1002/..
 
?
10

Promises and pitfalls of whole-exome sequencing exemplified..:

Guaragna, Mara Sanches ; de Brito Lutaif, Anna Cristina Gervásio ; de Souza, Marcela Lopes...
Molecular Genetics and Genomics.  295 (2019)  1 - p. 135-142 , 2019
Link: https://doi.org/10.1007/..
 
?
11

PAPSS2 gene molecular analysis in 46,XX patients with idiop..:

Mello, Maricilda Palandi de ; Guerra Júnior, Gil ; Marini, Sofia Helena Valente de Lemos...
Revista dos Trabalhos de Iniciação Científica da UNICAMP.  , 2019
Link: https://doi.org/10.20396..
 
?
12

Funcional analysis of variants in NPHS2 promoter identified..:

Mello, Maricilda Palandi de ; Guerra Júnior, Gil ; Belangero, Vera Maria Santoro...
Revista dos Trabalhos de Iniciação Científica da UNICAMP.  , 2019
Link: https://doi.org/10.20396..
 
?
13

Dopamine D2 receptor gene polymorphisms and externalizing b..:

Della Torre, Osmar Henrique ; Paes, Lúcia Arisaka ; Henriques, Taciane Barbosa...
BMC Medical Genetics.  19 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
?
14

A study of splicing mutations in disorders of sex developme..:

de Calais, Flavia Leme ; Smith, Lindsay D. ; Raponi, Michela...
Scientific Reports.  7 (2017)  1 - p. , 2017
Link: https://doi.org/10.1038/..
 
?
15

Development of CYP21A2 Genotyping Assay for the Diagnosis o..:

Prado, Mayara Jorgens ; de Castro, Simone Martins ; Kopacek, Cristiane...
Molecular Diagnosis & Therapy.  21 (2017)  6 - p. 663-675 , 2017
Link: https://doi.org/10.1007/..
 
1-15