Browsing Centre for Endocrinology by Title
Now showing items 152-171 of 556
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Familial Glucocorticoid Deficiency: the changing landscape of an eponymous syndrome.
(Frontiers Media, 2023-12-21)Familial Glucocorticoid Deficiency encompasses a broad spectrum of monogenic recessive disorders that theoretically solely abrogate cortisol biosynthesis. In reality, delineating clear genotype-phenotype correlations in ... -
Fatal Carney Complex in Siblings Due to De Novo Large Gene Deletion.
(2017-11-01)Context: Carney complex (CNC) is a rare multiple neoplasia syndrome involving cardiac, endocrine, neural, and cutaneous tumors and a variety of pigmented skin lesions. CNC can be inherited as an autosomal dominant trait, ... -
Fever, jaundice and acute renal failure
(2015-02) -
Fibroblast state switching orchestrates dermal maturation and wound healing
(EMBO, 2018-08-29) -
Focus on acute kidney injury 2017
(2018-11) -
From pituitary adenoma to pituitary neuroendocrine tumor (PitNET): an International Pituitary Pathology Club proposal.
(2017-04)The classification of neoplasms of adenohypophysial cells is misleading because of the simplistic distinction between adenoma and carcinoma, based solely on metastatic spread and the poor reproducibility and predictive ... -
Genes underlying delayed puberty
(2018-11-15) -
Genetic analysis of pediatric primary adrenal insufficiency of unknown etiology: 25 years’ experience in the UK
(Oxford University Press, 2021-05-12)Context Although primary adrenal insufficiency (PAI) in children and young people is often due to congenital adrenal hyperplasia (CAH) or autoimmunity, other genetic causes occur. The relative prevalence of these conditions ... -
Genetic Aspects of Pituitary Adenomas
(2017-06) -
The genetic background of acromegaly.
(2017-02)Acromegaly is caused by a somatotropinoma in the vast majority of the cases. These are monoclonal tumors that can occur sporadically or rarely in a familial setting. In the last few years, novel familial syndromes have ...