Results 261 to 270 of about 294,683 (378)

International Union of Basic and Clinical Pharmacology. XCIII. The Parathyroid Hormone Receptors—Family B G Protein–Coupled Receptors

Pharmacological Reviews, 2015
T. Gardella, J. Vilardaga
semanticscholar   +1 more source

Bilateral internal jugular vein (BIJV) sampling during surgery for primary hyperparathyroidism (PHPT) - scoping review of evidence and search for an optimal definition for lateralisation. [PDF]

Langenbecks Arch Surg
Prakash V, Kamalakkannan N, Balasubramanian SP.   +2 more
europepmc   +1 more source

Parathyroid hormone: anabolic and catabolic actions on the skeleton.

Current opinion in pharmacology (Print), 2015
B. C. Silva, J. Bilezikian
semanticscholar   +1 more source

Burosumab in Unidentifiable Tumor‐Induced Osteomalacia

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Tumor‐induced osteomalacia (TIO) can be challenging due to underlying tumors being either unresectable or unidentifiable. Burosumab, an anti‐FGF23 monoclonal antibody, has been proven to be effective in treating TIO but is currently not subsidized for this indication in Australia.
Yi Shan Der, Santosh Chaubey, Anna Mclean, Yasmin Trinh, Shelley Pember, Ashim Sinha   +5 more
wiley   +1 more source

Large atypical parathyroid tumor mimicking metastatic papillary thyroid carcinoma: a case report. [PDF]

J Med Case Rep
Wang A, Zhou Y, Zhang X, Wang X, Xue X, Huang J, Wang S, Li C.   +7 more
europepmc   +1 more source

Detecting the Near Infrared Autofluorescence of the Human Parathyroid

, 2019
Carmen C. Solórzano, Giju Thomas, Naira Baregamian, Anita Mahadevan‐Jansen   +3 more
openalex   +2 more sources

Genetics of parathyroid tumours

Journal of Internal Medicine, 2016
R. Thakker
semanticscholar   +1 more source

Incidental Diagnosis of Fahr's Disease Following Severe Traumatic Brain Injury: A Case Report

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Fahr's disease is a rare idiopathic neurodegenerative disorder characterized by symmetrical calcifications in the basal ganglia and cerebellar dentate nuclei. Although it may present with diverse neuropsychiatric symptoms, a significant number of cases remain asymptomatic and are only identified incidentally through neuroimaging performed for ...
Hadi Ebrahimi, Ali Holakoo, Seyyed Ebrahim Hejazian, Hamed Ahmadian, Amir Hosein Zohrevand, Morteza Sharifzadeh   +5 more
wiley   +1 more source

Released Granulocytic Elastase [PDF]

, 1985
Duswald, Karl-Heimo, Fritz, Hans, Jochum, Marianne, Schramm, Wolfgang   +3 more
core  

Novel Genetic Findings in Stuve‐Wiedemann Syndrome: A Case Report and Review of Literature

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Stuve‐Wiedemann Syndrome (SWS) is a rare autosomal recessive condition, first reported in 1971 by Stuve and Wiedemann. It is associated with pathogenic or likely pathogenic homozygous or compound heterozygous variants in the Leukemia Inhibitory Factor Receptor (LIFR) gene.
Khalid Hamasalih Hamasharef, Zana Baqi Najmadden, Rozhgar AKhailany, Muhammad Jabar Rashid, Kaiwan Hamakarim   +4 more
wiley   +1 more source