Centre for Endocrinology: Recent submissions
Now showing items 341-360 of 560
-
Delayed Puberty-Phenotypic Diversity, Molecular Genetic Mechanisms, and Recent Discoveries.
(2019-10-01)This review presents a comprehensive discussion of the clinical condition of delayed puberty, a common presentation to the pediatric endocrinologist, which may present both diagnostic and prognostic challenges. Our ... -
3T MRI evaluation of regional catecholamine-producing tumor-induced myocardial injury.
(2019-05-01)Objective: Regional differences in cardiac magnetic resonance, which can reveal catecholamine-induced myocardial injury in patients with pheochromocytoma, have not yet been assessed using 3T magnetic resonance imaging. We ... -
Isolated glucocorticoid deficiency: Genetic causes and animal models.
(Elsevier Ltd., 2019-02-25)Hereditary adrenocorticotropin (ACTH) resistance syndromes encompass the genetically heterogeneous isolated or Familial Glucocorticoid Deficiency (FGD) and the distinct clinical entity known as Triple A syndrome. The ... -
Diffusion‐weighted imaging (DWI) highlights SDHB ‐related tumours: A pilot study
(John Wiley & Sons Ltd, 2019-04-11)OBJECTIVE: There is consensus that asymptomatic carriers of SDHB mutations should undergo periodic surveillance imaging. MRI has the advantage of avoiding radiation exposure but its sensitivity and specificity for detecting ... -
The Roles of YAP/TAZ and the Hippo Pathway in Healthy and Diseased Skin
<jats:p>Skin is the largest organ of the human body. Its architecture and physiological functions depend on diverse populations of epidermal cells and dermal fibroblasts. Reciprocal communication between the epidermis and ... -
Can subunit-specific phenotypes guide surveillance imaging decisions in asymptomatic SDH mutation carriers?
(John Wiley & Sons Ltd, 2019-11-28)Objective With the discovery that familial phaeochromocytoma and paraganglioma syndrome can be caused by mutations in each subunit of the succinate dehydrogenase enzyme (SDH), has come the recognition that mutations in ... -
Reply to Chi et al.
(Elsevier BV, 2016-10-27) -
Novel Germline p.Gly42Val MEN1 Mutation in a Family with Multiple Endocrine Neoplasia Type 1 - Excellent Response of Prolactinoma to Cabergoline.
(2017-09)We report on a 27-year-old male patient presenting with renal colic secondary to hyperparathyroidism. Further investigations confirmed a diagnosis of type 1 multiple endocrine neoplasia and revealed a 2.0 cm pancreatic ... -
Mutant Lef1 controls Gata6 in sebaceous gland development and cancer
(EMBO, 2019-05-02) -
Wounding induces dedifferentiation of epidermal Gata6+ cells and acquisition of stem cell properties
(Springer Nature, 2017-06) -
Skin Cell Heterogeneity in Development, Wound Healing, and Cancer
(Elsevier BV, 2018-09) -
Inhibition of β-catenin signalling in dermal fibroblasts enhances hair follicle regeneration during wound healing
(The Company of Biologists, 2016-07-15) -
Fibroblast state switching orchestrates dermal maturation and wound healing
(EMBO, 2018-08-29)