Zobrazeno 1 - 10
of 139
pro vyhledávání: '"S Croxson"'
Autor:
Talia L. Fuchs, Catherine Luxford, Adele Clarkson, Amy Sheen, Loretta Sioson, Marianne Elston, Michael S. Croxson, Trisha Dwight, Diana E. Benn, Lyndal Tacon, Michael Field, Mahsa S. Ahadi, Angela Chou, Roderick J. Clifton-Bligh, Anthony J. Gill
Publikováno v:
American Journal of Surgical Pathology. 47:25-36
Up to 40% of pheochromocytomas (PCCs) and paragangliomas (PGLs) are hereditary. Germline mutations/deletions in fumarate hydratase ( FH ) cause hereditary leiomyomatosis and renal cell carcinoma syndrome which manifests predominantly with FH-deficien
Autor:
Mark J Bolland, Michael S Croxson
BackgroundRadioiodine is commonly prescribed as a permanent treatment for thyrotoxicosis. At ADHB, Auckland, New Zealand, radioiodine dose is individualised by the prescribing physician according to patient characteristics.AimsWe investigated the out
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45c7555f98cf70e94b407f337086de52
https://doi.org/10.1101/2022.01.17.22269444
https://doi.org/10.1101/2022.01.17.22269444
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 84:452-457
Objective To determine the frequency and range of neurological manifestations of phaeochromocytomas and secretory paragangliomas. Methods A retrospective review of case notes of patients admitted to Auckland Hospital from 1985 to 2011 with a discharg
Publikováno v:
Journal of Medical Imaging and Radiation Oncology. 53:177-187
The role for ultrasound (US) in the assessment of nodular thyroid disease has increased in recent years. This expanded role has been highlighted in recent consensus guidelines on the management of nodular thyroid disease. In this review, we address t
Autor:
Patrick J. Manning, G. Smith, Peter M. George, S. Farrand, H. C. Potter, Christopher M. Florkowski, M. S. Croxson, B. E. W. Brownlie
Publikováno v:
Internal Medicine Journal. 36:738-741
The finding of increased thyroxine (T4) and tri-iodothyronine (T3) levels in a patient with normal or increased thyroid-stimulating hormone is unexpected and presents a differential diagnosis between a thyroid-stimulating hormone-secreting pituitary
Publikováno v:
Thyroid. 22:651-653
Anterior compartment syndrome (ACS) and rhabdomyolysis are rare complications of hypothyroid myopathy. We report the case of a young man with rapid onset of ACS who presented with simultaneous primary hypothyroidism and adrenal insufficiency associat
Autor:
S. Croxson
Publikováno v:
Diabetic Medicine. 19:66-72
Diabetes is common in the elderly and old UK citizens, affecting between 10% and 25%. There is considerable associated morbidity and mortality, with dementia being a common problem. The diabetic elder is also at risk of drug side-effects. Most of the
Publikováno v:
BMJ Case Reports. :bcr-2017
A 23-year-old man presenting with florid Cushing's syndrome was found to have high plasma ACTH and very high serum prolactin. Pituitary MRI showed a large invasive macroadenoma. Low-dose cabergoline promptly suppressed both ACTH and prolactin levels
Publikováno v:
NDT Plus
Hypertension is common in patients with end stage renal disease. However, in patients non-responsive to standard measures to control the blood pressure, non-renal causes should be considered. We present the case of a patient on haemodialysis with dif
Publikováno v:
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine. 43:237-239
We investigated a patient with suspected hypopituitarism who showed subnormal cortisol responses to stimulation tests with adrenocorticotrophic hormone (ACTH) and hypoglycaemia, but normal ACTH and 11-deoxycortisol responses in the metyrapone test. C