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Lista de obras de Duarte Pignatelli

21-Hydroxylase–deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study

artículo científico publicado en 2000

ACTH modulates ERK phosphorylation in the adrenal gland in a time-dependent manner

artículo científico publicado en 2004

Absence of central circadian pacemaker abnormalities in humans with loss of function mutation in prokineticin 2

artículo científico publicado en 2014

Adrenarche in the rat

scientific journal article

Chronic exposure of rats to occupational textile noise causes cytological changes in adrenal cortex

artículo científico publicado en 2009

Congenital Hypogonadotropic Hypogonadism and Constitutional Delay of Growth and Puberty Have Distinct Genetic Architectures

artículo científico publicado en 2018

Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism

artículo científico publicado en 2017

Effects of prolonged infusion of basic fibroblast growth factor and IGF-I on adrenocortical differentiation in the autotransplanted adrenal: an immunohistochemical study

artículo científico publicado en 1999

European survey of diagnosis and management of the polycystic ovary syndrome: results of the ESE PCOS Special Interest Group's Questionnaire

artículo científico publicado en 2014

IGF2 role in adrenocortical carcinoma biology

artículo científico publicado en 2019

Immunohistochemical study of heat shock proteins 27, 60 and 70 in the normal human adrenal and in adrenal tumors with suppressed ACTH production.

artículo científico publicado en 2003

Increased extracellular signal regulated kinases phosphorylation in the adrenal gland in response to chronic ACTH treatment

article

Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

artículo científico publicado en 2007

MAPK/ERK pathway inhibition is a promising treatment target for adrenocortical tumors

artículo científico publicado en 2018

Melanocortin 5 receptor activates ERK1/2 through a PI3K-regulated signaling mechanism.

artículo científico publicado en 2009

Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD) reveals novel mutations and clues for pathophysio

artículo científico publicado en 2002

Mutational characterization of steroid 21-hydroxylase gene in Portuguese patients with congenital adrenal hyperplasia

artículo científico publicado en 2009

Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum.

artículo científico publicado en 2008

Non-classic adrenal hyperplasia due to the deficiency of 21-hydroxylase and its relation to polycystic ovarian syndrome

artículo científico publicado en 2012

Novel FGFR1 mutations in Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: evidence for the involvement of an alternatively spliced isoform

artículo científico publicado en 2015

Proliferation of capsular stem cells induced by ACTH in the rat adrenal cortex

artículo científico publicado en 2002

Reproductive outcome of women with 21-hydroxylase-deficient nonclassic adrenal hyperplasia.

artículo científico publicado en 2006

The development of the adrenal gland zona glomerulosa in the rat. A morphological, immunohistochemical and biochemical study

artículo científico publicado en 1998

The polycystic ovary syndrome: a position statement from the European Society of Endocrinology

artículo científico publicado en 2014

Unilateral adrenal hyperplasia

scientific article published on 01 June 1994

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