Adriana Mangue Esquiaveto-Aun

ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 4

Top Venues

American journal of medical genetics. Part A

Diabetology & metabolic syndrome

This page only lists publications with an associated author ORCID identifier.

Publications

Adriana Mangue Esquiaveto-Aun, Maricilda Palandi de Mello, Mara Sanches Guaragna, Vera Lúcia Gil da Silva Lopes, Ana Paula Francese-Santos, Cristiane Dos Santos Cruz Piveta, Taís Nitsh Mazolla, Sofia Helena Valente de Lemos-Marini, Gil Guerra-Junior
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 194 (6) (2024)
Adriana Mangue Esquiaveto-Aun, Maricilda Palandi de Mello, Mara Sanches Guaragna, Vera Lúcia Gil da Silva Lopes, Ana Paula Francese-Santos, Cristiane Dos Santos Cruz Piveta, Taís Nitsh Mazolla, Sofia Helena Valente de Lemos-Marini, Gil Guerra-Junior
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 194 (6) (2024)
Adriana Mangue Esquiaveto-Aun, Maricilda Palandi de Mello, Mara Sanches Guaragna, Vera Lúcia Gil da Silva Lopes, Ana Paula Francese-Santos, Cristiane Dos Santos Cruz Piveta, Taís Nitsh Mazolla, Sofia Helena Valente de Lemos-Marini, Gil Guerra-Junior
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 (2024)
Adriana Mangue Esquiaveto-Aun, Maricilda Palandi de Mello, Mara Sanches Guaragna, Vera Lúcia Gil da Silva Lopes, Ana Paula Francese-Santos, Cristiane Dos Santos Cruz Piveta, Taís Nitsh Mazolla, Sofia Helena Valente de Lemos-Marini, Gil Guerra-Junior
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 194 (6) (2024)
Adriana Mangue Esquiaveto-Aun, Maricilda Palandi De Mello, Maria Fernanda Vanti Macedo Paulino, Walter José Minicucci, Gil Guerra-Júnior, Sofia Helena Valente De Lemos-Marini
A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins. Diabetology & metabolic syndrome 7 (2015)

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Publication Activity (10 Years)

Top Topics

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Adriana Mangue Esquiaveto-Aun