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Author/Creator Correa, Fernanda A

1. A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD). Issue 2 (August 2016)

Authors:
Madeira, João L O; Jorge, Alexander A L; Martin, Regina M; Montenegro, Luciana R; Franca, Marcela M; Costalonga, Everlayny F; Correa, Fernanda A; Otto, Aline P; Arnhold, Ivo J P; Freitas, Helayne S; Machado, Ubiratan F; Mendonca, Berenice B; Carvalho, Luciani R
Journal:
European journal of endocrinology
Issue:
Volume 175:Issue 2(2016)
Page Start:
K7
Record Type:
Journal Article
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2. Genetic diagnosis of congenital hypopituitarism by a target gene panel: novel pathogenic variants in GLI2, OTX2 and GHRHR. Issue 5 (May 2019)

Authors:
Nakaguma, Marilena; Correa, Fernanda A; Santana, Lucas S; Benedetti, Anna F F; Perez, Ricardo V; Huayllas, Martha K P; Miras, Mirta B; Funari, Mariana F A; Lerario, Antonio M; Mendonca, Berenice B; Carvalho, Luciani R S; Jorge, Alexander A L; Arnhold, Ivo J P
Journal:
Endocrine connections
Issue:
Volume 8:Issue 5(2019)
Page Start:
590
Record Type:
Journal Article
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3. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations. (4th September 2017)

Authors:
Madeira, Joao LO; Nishi, Mirian Y; Nakaguma, Marilena; Benedetti, Anna F; Biscotto, Isabela Peixoto; Fernandes, Thamiris; Pequeno, Thiago; Figueiredo, Thalita; Franca, Marcela M; Correa, Fernanda A; Otto, Aline P; Abrão, Milena; Miras, Mirta B; Santos, Silvana; Jorge, Alexander AL; Costalonga, Ev...
Journal:
Clinical endocrinology
Issue:
Volume 87:Number 6(2017)
Page Start:
725
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗