Results 91 to 100 of about 4,881,171 (274)

Urinary Calcium Measurement in Patients With Hypercalcaemia; Endocrine Physicians and Surgeons Survey Results From UK

open access: yesClinical Endocrinology, Volume 103, Issue 5, Page 757-760, November 2025.
ABSTRACT Background In patients with hypercalcaemia, assessment of urinary calcium excretion helps differentiate primary hyperparathyroidism (PHPT) from familial hypocalciuric hypercalcaemia (FHH). For this, 24 h calcium to creatinine clearance ratio (CCCR) is recommended, but others tests like random CCCR, 24 h urine calcium excretion (UCE), and ...
Muhammad Fahad Arshad   +1 more
wiley   +1 more source

Selection of DNA Aptamers Against Parathyroid Hormone for Electrochemical Impedimetric Biosensor System Development

open access: yesBiotechnology and Applied Biochemistry, Volume 72, Issue 5, Page 1351-1362, October 2025.
ABSTRACT This work presents the pioneering development of an aptamer‐based electrochemical biosensor for real‐time monitoring of parathyroid hormone (PTH) levels, with a focus on intraoperative assessment during parathyroid surgery. It introduces, for the first time, the selection and characterization of aptamers targeting distinct segments of the PTH ...
Reza Didarian   +5 more
wiley   +1 more source

Primary hyperparathyroidism and metastatic breast carcinoma: A case in which breast carcinoma metastasized to a parathyroid adenoma [PDF]

open access: bronze, 1958
Lewis B. Woolner   +2 more
openalex   +1 more source

Apoptosis in Primary Hyperparathyroidism

open access: yesJournal of Investigative Surgery, 2017
Primary hyperparathyroidism (PHPT) is defined by inappropriate elevation of parathormone, caused by parathyroid hyperplasia, also known as multi-gland disease (MGD), parathyroid adenoma (PA), or parathyroid carcinoma (PC). Although several studies have already been conducted, there is a lack of a definite diagnostic marker, which could unambiguously ...
Łukasz Mielańczyk   +7 more
openaire   +4 more sources

DIAGNOSIS AND TREATMENT OF PRIMARY HYPERPARATHYROIDISM: CLINICAL CASE

open access: yesŽurnal Grodnenskogo Gosudarstvennogo Medicinskogo Universiteta, 2019
A clinical case of primary hyperparathyroidism revealed in the endocrinology department of the Grodno Regional Clinical Hospital is presented. The article describes the modern diagnostics and tactics of successful treatment of the patient with primary ...
Martinkevich O. N.   +4 more
doaj   +1 more source

Familial Multiple Endocrine Adenopathy (Primary Hyperparathyroidism and Zollinger-Ellison Syndrome) in Two Siblings [PDF]

open access: bronze, 1968
Purnendu Dutta   +4 more
openalex   +1 more source

Roxadustat for ESA‐Hyporesponsive Renal Anemia in a 13‐Year‐Old on Hemodialysis: Case Report and Mini‐Review

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
Changes in hemoglobin and iron metabolism parameters during Roxadustat treatment in a 13‐year‐old dialysis patient. ABSTRACT Anemia is the most common complication of end‐stage renal disease (ESRD). While erythropoiesis‐stimulating agents (ESA) have improved treatment outcomes, some patients exhibit intolerance or hyporesponsiveness.
Meng Zhang   +3 more
wiley   +1 more source

Pathophysiology of primary hyperparathyroidism.

open access: yesHistology and histopathology, 2000
Parathyroid gland is the overall regulatory organ within the systemic calcium homeostasis. Through cell surface bound calcium-sensing receptors external calcium inversely regulates release of parathyroid hormone (PTH). This mechanism, which is voltage independent and most sensitive around physiologic calcium concentrations, is regulated through a 120 ...
Hellman, P.   +3 more
openaire   +4 more sources

Untying the Next Genetic Thread in a Family With MEN2A Syndrome: A Case Report

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Multiple endocrine neoplasia type 2A (MEN2A) is a rare autosomal dominant syndrome characterized by medullary thyroid carcinoma (MTC), pheochromocytoma, and primary hyperparathyroidism. Early genetic screening is crucial for timely intervention. We report a familial case of MEN2A involving four affected members across two generations.
Riyaz Shrestha   +6 more
wiley   +1 more source

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