Browsing by Author Pignatelli, D

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Showing results 1 to 10 of 10
Issue DateTitleAuthor(s)Type
2021Angiogenesis in the Normal Adrenal Fetal Cortex and Adrenocortical TumorsPereira, SS; Oliveira, S; Monteiro, M; Pignatelli, DOutra Publicação em Revista Científica Internacional
2019Apoptosis regulation in adrenocortical carcinomaPereira, SS; Monteiro, MP; Antonini, SR; Pignatelli, DArtigo em Revista Científica Internacional
2020Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase DeficiencyPignatelli, D; Carvalho, B; Palmeiro, A; Barros, A; Guerreiro, SG; Macut, DOutra Publicação em Revista Científica Internacional
2021How Relevant is the Systemic Oxytocin Concentration for Human Sexual Behavior? A Systematic ReviewCera, N; Vargas-Cáceres, S; Oliveira, C; Monteiro, J; Branco, D; Pignatelli, D; Rebelo, SArtigo em Revista Científica Internacional
2020Incomplete pattern of steroidogenic protein expression in functioning adrenocortical carcinomasPereira, SS; Costa, MM; Gomez-Sanchez, CE; Monteiro, MP; Pignatelli, DArtigo em Revista Científica Internacional
2020Incomplete Pattern of Steroidogenic Protein Expression in Functioning Adrenocortical CarcinomasPereira, SS; Costa, MM; Gomez Sanchez, CE; Monteiro, M; Pignatelli, DArtigo em Revista Científica Internacional
2009Melanocortin 5 receptor activates ERK1/2 through a PI3K-regulated signaling mechanismRodrigues, AR; Pignatelli, D; Almeida, Henrique; Gouveia, AlexandraArtigo em Revista Científica Internacional
2019Metabolic Perspectives for Non-classical Congenital Adrenal Hyperplasia With Relation to the Classical Form of the DiseaseMacut, D; Zdravkovic, V; Bjekic-Macut, J; Mastorakos, G; Pignatelli, DArtigo em Revista Científica Internacional
2021Mineralocorticoid receptor antagonists eplerenone and spironolactone modify adrenal cortex morphology and physiologyPereira, SS; Carvalho, LS; Costa, MM; Melo, A; Ferreira, IMPLVO; Gomez-Sanchez, CE; Monteiro, MP; Vinson, G; Pignatelli, DArtigo em Revista Científica Internacional
2019The complexities in genotyping of congenital adrenal hyperplasia: 21-hydroxylase deficiencyPignatelli, D; Carvalho, B; Palmeiro, A; Barros, A; Guerreiro, SG; Macut, DArtigo em Revista Científica Internacional