Results 11 to 20 of about 25,224 (147)

Identification of de Novo Germline Mutations in the HRPT2 Gene in Two Apparently Sporadic Cases with Challenging Parathyroid Tumor Diagnoses [PDF]

open access: yes, 2011
The diagnosis of parathyroid carcinomas is often difficult. HRPT2 mutations have been identified in familial [hyperparathyroidism-jaw tumor (HPT-JT) syndrome] and sporadic parathyroid carcinomas, supporting that HRPT2 mutations may confer a malignant ...
Carvalho, D   +11 more
core   +1 more source

Clinical and molecular genetics of parathyroid neoplasms [PDF]

open access: yesBest Practice & Research Clinical Endocrinology & Metabolism, 2010
Primary hyperparathyroidism (HPT) results from the excessive secretion of parathyroid hormone from parathyroid tumours. While most HPT is sporadic, it is associated with a familial syndrome in a minority of cases. The study of these syndromes has helped define the pathophysiology of both familial and sporadic parathyroid neoplasms.
John M, Sharretts, William F, Simonds
openaire   +2 more sources

Salivary gland choristoma in the buccinator muscle: a case report and literature review [PDF]

open access: yes, 2015
Salivary gland choristoma (SGCh) is defined as the presence of normal salivary tissue in an abnormal location. It is a rare entity in oral and maxillofacial region and its ethiology is unknown.
Almendros Marqués, Nieves   +4 more
core   +2 more sources

Parathyroid adenoma completely impacted within the thyroid gland: A case report [PDF]

open access: yes, 2016
Ectopic parathyroid adenoma can be seen in various locations. Sometimes ultrasound and even fine needle aspiration studies cannot distinguish this lesion from thyroid lesions.
Amani, Soroush.   +2 more
core   +1 more source

Discordant Findings of Skeletal Metastasis Between Tc99m MDP Bone Scans and F18 FDG PET/CT Imaging for Advanced Breast and Lung Cancers—Two Case Reports and Literature Review [PDF]

open access: yes, 1929
Traditionally, Tc99m methyl diphosphate (MDP) bone scintigraphy provides high-sensitivity detection of skeletal metastasis from breast and lung cancers in regular follow-up.
Chen, Yu-Wen   +5 more
core   +2 more sources

Chromogranin A: From Laboratory to Clinical Aspects of Patients with Neuroendocrine Tumors [PDF]

open access: yes, 2018
Background. Neuroendocrine tumors (NETs) are characterized by having behavior and prognosis that depend upon tumor histology, primary site, staging, and proliferative index.
Baldelli, Roberto   +8 more
core   +1 more source

Role of key players in paradigm shifts of prostate cancer bone metastasis [PDF]

open access: yes, 2018
Prostate cancer is one of the most common human cancers and bone metastasis is a frequent finding in the natural history of several types of cancers. The molecular mechanisms that makes prostate cancer metastasize to bone have recently been identified, and
Beg, OA   +6 more
core   +2 more sources

IMMUNOCHEMICAL IDENTIFICATION OF PARATHYROID HORMONE IN NON-PARATHYROID NEOPLASMS ASSOCIATED WITH HYPERCALCEMIA [PDF]

open access: yesThe Journal of Experimental Medicine, 1964
1. Immunochemical cross-reactivity, but not identity, has been demonstrated between bovine parathyroid hormone and an antigen in biologically active extracts of human parathyroid tissue by quantitative C' fixation and C' fixation inhibition. 2.
A H, TASHJIAN, L, LEVINE, P L, MUNSON
openaire   +2 more sources

Parathyroid Neoplasms: The Army Hospital (Research & Referral) Experience [PDF]

open access: yesMedical Journal Armed Forces India, 2006
Neoplasms of the parathyroid are common but parathyroid carcinoma is exceptionally rare. In contrast to most other malignant endocrine tumours that are usually less hormonally active, malignant parathyroid tumours are hyper functional. Malignant parathyroid tumours pose a diagnostic dilemma for the pathologist.To study the clinicopathological profile ...
B, Fanthome   +2 more
openaire   +2 more sources

Angiosarcoma at the site of nonfunctioning arteriovenous fistula in a kidney transplant recipient [PDF]

open access: yes, 2011
Angiosarcoma is a rare malignant neoplasm of the endothelial cells of blood vessels or lymphatics. We report a case of a 46-year-old male patient with a kidney transplant who developed epithelioid angiosarcoma at the site of a nonfunctioning ...
Young   +19 more
core   +2 more sources

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