Results 151 to 160 of about 370,756 (269)

Primary hyperparathyroidism in a domestic shorthair cat following I131 radioiodine therapy

Journal of Small Animal Practice, EarlyView.
A 12‐year‐old male neutered domestic shorthaired cat presented for further assessment of a cervical mass, having undergone radioiodine therapy for treatment of hyperthyroidism 2 years prior to presentation. Initial cytological diagnosis of the mass was supportive of a carcinoma and laboratory results were consistent with primary hyperparathyroidism ...
E. Ruane, P. Odatzoglou, H. Wong, A. Hayes   +3 more
wiley   +1 more source

Mediastinal Parathyroid Adenoma Mimicking Cancer Metastatic to Bone

AACE Clinical Case Reports, 2017
: Objective: Mediastinal parathyroid adenomas are rare in clinical practice. We report a case that mimicked cancer metastatic to bone on initial workup to increase awareness of this differential diagnosis in the evaluation of patients presenting with ...
Ping Yu Xiong, MD, Joshua Lakoff, MD, FRCPC, Robyn L. Houlden, MD, FRCPC   +2 more
doaj  

A Brown Tumor Simulating Bone Metastases

Case Reports in Clinical Practice, 2016
Primary hyperparathyroidism usually presents with renal, gastrointestinal, mental and skeletal signs and symptoms. Brown tumor is a benign lesion that arises as a direct result of parathyroid hormone on bone tissue in some patients with ...
Neda Naderi, Azam Alamdari, Maryam Edalatifard, Seyyed Farshad Allameh   +3 more
doaj  

Detection of renal tubular transporter proteins in canine urinary extracellular vesicles using liquid chromatography–tandem mass spectrometry

Veterinary Clinical Pathology, EarlyView.
Abstract Urinary extracellular vesicles (UEVs) are membranous particles that carry renal tubular transporter proteins. Here, we evaluate whether selected renal tubular transporter proteins can be detected in UEVs isolated from small volume (1–5 mL) canine urine samples of healthy dogs and canine patients with elevated circulating parathyroid hormone ...
L. J. McGravey, P. R. Antrobus, T. L. Williams   +2 more
wiley   +1 more source

A case of synchronous hurthle cell adenoma of thyroid and para thyroid adenoma

Iranian South Medical Journal, 2015
Synchronous hurthle cell adenoma of thyroid and para thyroid adenoma is very rare .Here we dicuss a 46 year old woman who presented with a thyroid nodule. Thyroid function test was normal but she had mild hypercalcemia.
Masoome Tohidi, Mohammadreza Kalantar Hormozi, Iraj Nabipour, Majid Assadi, Fariba Karimi   +4 more
doaj  

Women in space: A review of known physiological adaptations and health perspectives

Experimental Physiology, EarlyView.
Abstract Exposure to the spaceflight environment causes adaptations in most human physiological systems, many of which are thought to affect women differently from men. Since only 11.5% of astronauts worldwide have been female, these issues are largely understudied.
Millie Hughes‐Fulford, Danielle J. Carroll, Heather C. M. Allaway, Bonnie J. Dunbar, Aenor J. Sawyer   +4 more
wiley   +1 more source

Palpable parathyroid adenomas presenting as clinical solitary thyroid nodules and cytologically as follicular thyroid neoplasms [PDF]

, 2003
Michael Weymouth, Jonathan W. Serpell, David Chambers   +2 more
openalex   +1 more source

Shear wave elastography for differentiating parathyroid neoplasms with malignant diagnosis or uncertain malignant potential from parathyroid adenomas: initial experience [PDF]

, 2022
Ruifeng Liu, Luying Gao, Xinlong Shi, Liyuan Ma, Ou Wang, Weibo Xia, Ya Hu, Yu Xia, Yuxin Jiang   +8 more
openalex   +1 more source

Molecular pathophysiology of chronic kidney disease–mineral and bone disorder: Focus on the fibroblast growth factor 23–Klotho axis and bone turnover dynamics

Experimental Physiology, EarlyView.
Abstract Chronic kidney disease–mineral and bone disorder (CKD‐MBD) is a major complication of chronic kidney disease (CKD), characterized by disruptions in mineral metabolism, abnormal bone turnover and vascular calcification, which collectively increase the risk of fractures and cardiovascular disease.
Alief Waitupu, Laras Pratiwi, Henry Sutanto, Djoko Santoso, Decsa Medika Hertanto   +4 more
wiley   +1 more source

Calcinosis cutis of the lower legs – hyperphosphatemic familial tumoral calcinosis in a patient with GALNT3 mutation

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
David Ranzinger, Tobias Schaefer, Franziska Schauer, Kilian Eyerich, Anna Caroline Pilz   +4 more
wiley   +1 more source