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Central adrenal insufficiency: who, when, and how? From the evidence to the controversies – an exploratory review
Central adrenal insufficiency: who, when, and how? From the evidence to the controversies – an exploratory review
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Central adrenal insufficiency: who, when, and how? From the evidence to the controversies – an exploratory review

Bitencourt, Mariana Rechia ; Batista, Rafael Loch ; Biscotto, Isabela ; Carvalho, Luciani R.

Archives of Endocrinology and Metabolism, 2022-07, Vol.66 (4), p.541-550

Sociedade Brasileira de Endocrinologia e Metabologia

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2
Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery
Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery
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Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery

Correa, Fernanda A. ; Nakaguma, Marilena ; Madeira, João L. O. ; Nishi, Mirian Y. ; Abrão, Milena G. ; Jorge, Alexander A. L. ; Carvalho, Luciani R. ; Arnhold, Ivo J. P. ; Mendonça, Berenice B.

Archives of Endocrinology and Metabolism, 2019-05, Vol.63 (2), p.167-174

Sociedade Brasileira de Endocrinologia e Metabologia

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3
An activating mutation in the CRHR1 gene is rarely associated with pituitary-dependent hyperadrenocorticism in poodles
An activating mutation in the CRHR1 gene is rarely associated with pituitary-dependent hyperadrenocorticism in poodles
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An activating mutation in the CRHR1 gene is rarely associated with pituitary-dependent hyperadrenocorticism in poodles

De-Marco, Viviani ; Carvalho, Luciani R. ; Guzzo, Mariana F. ; Oliveira, Paulo S.L. ; Gomes, Larissa G. ; Mendonca, Berenice B.

Clinics (São Paulo, Brazil), 2017-10, Vol.72 (9), p.575-581 [Periódico revisado por pares]

Brazil: Elsevier España, S.L.U

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4
Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing
Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing
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Growth hormone deficiency with advanced bone age: phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing

Correa, Fernanda A. ; França, Marcela M. ; Fang, Qing ; Ma, Qianyi ; Bachega, Tania A. ; Rodrigues, Andresa ; Ozel, Bilge A. ; Li, Jun Z. ; Mendonca, Berenice B. ; Jorge, Alexander A. L. ; Carvalho, Luciani R. ; Camper, Sally A. ; Arnhold, Ivo J. P

Archives of Endocrinology and Metabolism, 2017-12, Vol.61 (6), p.633-636

Brazilian Society of Endocrinology and Metabolism

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5
PROP1 and CTNNB1 expression in adamantinomatous craniopharyngiomas with or without β-catenin mutations
PROP1 and CTNNB1 expression in adamantinomatous craniopharyngiomas with or without β-catenin mutations
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PROP1 and CTNNB1 expression in adamantinomatous craniopharyngiomas with or without β-catenin mutations

Cani, Carolina M.G. ; Matushita, Hamilton ; Carvalho, Luciani R.S. ; Soares, Ibere C. ; Brito, Luciana P. ; Almeida, Madson Q. ; Mendonça, Berenice B.

Clinics (São Paulo, Brazil), 2011-01, Vol.66 (11), p.1849-1854 [Periódico revisado por pares]

Brazil: Elsevier España, S.L.U

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6
PROP1 overexpression in corticotrophinomas: evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation
PROP1 overexpression in corticotrophinomas: evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation
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PROP1 overexpression in corticotrophinomas: evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation

Araujo, Ricardo V ; Chang, Claudia V ; Cescato, Valter A.S. ; Fragoso, Maria Candida B.V. ; Bronstein, Marcello D ; Mendonca, Berenice B ; Arnhold, Ivo J.P. ; Carvalho, Luciani R S

Clinics (São Paulo, Brazil), 2013-06, Vol.68 (6), p.887-891 [Periódico revisado por pares]

Brazil: Elsevier España, S.L.U

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