Tais N. Mazzola

Campinas, SP, Brazil

Last Updated: 09/26/2026

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Found 22 publications

Twelve Brazilian families with X-linked Congenital Adrenal Hypoplasia: new rearrangements and new variants in the NR0B1 gene.

Twelve Brazilian families with X-linked Congenital Adrenal Hypoplasia: new rearrangements and new variants in the NR0B1 gene.

Journal: Jornal de pediatria

Published: September 01, 2025

Phenotype Overlap and Lung Function in Childhood Asthma: The Interaction Between T2 and Non-T2 Responses.

Phenotype Overlap and Lung Function in Childhood Asthma: The Interaction Between T2 and Non-T2 Responses.

Journal: Pediatric pulmonology

Published: January 01, 2025

Neuropsychiatric manifestations in systemic lupus erythematosus and Sjogren's disease.

Neuropsychiatric manifestations in systemic lupus erythematosus and Sjogren's disease.

Journal: Autoimmunity reviews

Published: December 01, 2024

Patients with genital ambiguity referred without a sex definition: the relationship between clinical picture and defined sex of rearing.

Patients with genital ambiguity referred without a sex definition: the relationship between clinical picture and defined sex of rearing.

Journal: Jornal de pediatria

Published: December 27, 2023

Prenatal Findings in Postnatal Cases of Disorders of Sex Development: Experience from a Tertiary-Specialized Center in Brazil.

Prenatal Findings in Postnatal Cases of Disorders of Sex Development: Experience from a Tertiary-Specialized Center in Brazil.

Journal: Fetal diagnosis and therapy

Published: May 24, 2023

DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis.

DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis.

Journal: Life (Basel, Switzerland)

Published: February 28, 2023

Identification of single nucleotide variants in SLC26A9 gene in patients with cystic fibrosis (p.Phe508del homozygous) and its association to Orkambi® (Lumacaftor and Ivacaftor) response in vitro.

Identification of single nucleotide variants in SLC26A9 gene in patients with cystic fibrosis (p.Phe508del homozygous) and its association to Orkambi® (Lumacaftor and Ivacaftor) response in vitro.

Journal: Gene

Published: February 04, 2023

Sex dimorphism of weight and length at birth: evidence based on disorders of sex development.

Sex dimorphism of weight and length at birth: evidence based on disorders of sex development.

Journal: Annals of human biology

Published: October 11, 2022

SOX3 duplication in a boy with 46,XX ovotesticular disorder of sex development and his 46,XX sister with atypical genitalia: Probable germline mosaicism.

SOX3 duplication in a boy with 46,XX ovotesticular disorder of sex development and his 46,XX sister with atypical genitalia: Probable germline mosaicism.

Journal: American journal of medical genetics. Part A

Published: August 08, 2022

Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study.

Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study.

Journal: Sao Paulo medical journal = Revista paulista de medicina

Published: May 06, 2022

Effective combined antiretroviral therapy provides partial immune recovery to mycobacterial antigens in vertically infected, BCG-vaccinated youth living with HIV.

Effective combined antiretroviral therapy provides partial immune recovery to mycobacterial antigens in vertically infected, BCG-vaccinated youth living with HIV.

Journal: Tuberculosis (Edinburgh, Scotland)

Published: November 10, 2021

So, and if it is not congenital adrenal hyperplasia? Addressing an undiagnosed case of genital ambiguity.

So, and if it is not congenital adrenal hyperplasia? Addressing an undiagnosed case of genital ambiguity.

Journal: Italian journal of pediatrics

Published: September 01, 2021

Showing 1-12 of 22

Last Updated: 09/26/2026