Lista de obras -

A putative role for the aryl hydrocarbon receptor (AHR) gene in a patient with cyclical Cushing's disease

scientific article published on 29 January 2020

Aberrant Splicing of SDHC in Families With Unexplained Succinate Dehydrogenase-Deficient Paragangliomas

scientific article published on 16 June 2020

Case report of whole genome sequencing in the XY female: identification of a novel SRY mutation and revision of a misdiagnosis of androgen insensitivity syndrome

artículo científico publicado en 2016

Corticotrophin-releasing hormone (CRH) expression in the dermoid component of ovarian teratomas

artículo científico publicado en 2015

Cutaneous lichen amyloidosis in multiple endocrine neoplasia

artículo científico publicado en 2016

Dopa-testotoxicosis: disruptive hypersexuality in hypogonadal men with prolactinomas treated with dopamine agonists

artículo científico publicado en 2016

Fall in thyroid stimulating hormone (TSH) may be an early marker of ipilimumab-induced hypophysitis.

artículo científico publicado en 2018

Increased Prevalence of Germline Pathogenic <i>CHEK2</i> Variants in Individuals With Pituitary Adenomas

artículo científico publicado en 2024

Ipilimumab-induced hypophysitis in melanoma patients: an Australian case series

artículo científico

Ipilimumab-induced hypophysitis: early Australian experience

artículo científico publicado en 2014

Metabolic syndrome, diet and exercise

artículo científico publicado en 2016

Pituitary hyperplasia: case series and literature review of an under-recognised and heterogeneous condition

artículo científico publicado en 2015

Prolactin correction for adequacy of petrosal sinus cannulation may diminish diagnostic accuracy in Cushing's disease

artículo científico publicado en 2017

Rebound vertebral and non-vertebral fractures during denosumab interruption in a postmenopausal woman

scientific article published on 30 October 2018

Synchronous Nesidioblastosis, Endocrine Microadenoma, and Intraductal Papillary Mucinous Neoplasia in a Man Presenting With Hyperinsulinemic Hypoglycemia.

artículo científico publicado en 2016

The Genomic Landscape of Sporadic Prolactinomas

scientific article published on 01 December 2019

Vasculogenic hyperprolactinemia: severe prolactin excess in association with internal carotid artery aneurysms.

artículo científico publicado en 2017

Lista de obras de

A putative role for the aryl hydrocarbon receptor (AHR) gene in a patient with cyclical Cushing's disease

Aberrant Splicing of SDHC in Families With Unexplained Succinate Dehydrogenase-Deficient Paragangliomas

Case report of whole genome sequencing in the XY female: identification of a novel SRY mutation and revision of a misdiagnosis of androgen insensitivity syndrome

Corticotrophin-releasing hormone (CRH) expression in the dermoid component of ovarian teratomas

Cutaneous lichen amyloidosis in multiple endocrine neoplasia

Dopa-testotoxicosis: disruptive hypersexuality in hypogonadal men with prolactinomas treated with dopamine agonists

Fall in thyroid stimulating hormone (TSH) may be an early marker of ipilimumab-induced hypophysitis.

Increased Prevalence of Germline Pathogenic <i>CHEK2</i> Variants in Individuals With Pituitary Adenomas

Ipilimumab-induced hypophysitis in melanoma patients: an Australian case series

Ipilimumab-induced hypophysitis: early Australian experience

Metabolic syndrome, diet and exercise

Pituitary hyperplasia: case series and literature review of an under-recognised and heterogeneous condition

Prolactin correction for adequacy of petrosal sinus cannulation may diminish diagnostic accuracy in Cushing's disease

Rebound vertebral and non-vertebral fractures during denosumab interruption in a postmenopausal woman

Synchronous Nesidioblastosis, Endocrine Microadenoma, and Intraductal Papillary Mucinous Neoplasia in a Man Presenting With Hyperinsulinemic Hypoglycemia.

The Genomic Landscape of Sporadic Prolactinomas

Vasculogenic hyperprolactinemia: severe prolactin excess in association with internal carotid artery aneurysms.