Results 271 to 280 of about 1,237,427 (393)

Vitamin D Deficiency as a Risk Factor for Onset and Recurrence of Sudden Sensorineural Hearing Loss: A Prospective Cohort Study With Age‐Specific Analysis

open access: yesFood Science &Nutrition, Volume 14, Issue 1, January 2026.
Pure‐tone audiometry (0–120 dB HL) identified patients with sudden sensorineural hearing loss (SSNHL). Serum 25‐hydroxyvitamin D levels revealed deficient (< 20 ng/mL), insufficient (20–30 ng/mL), or sufficient (≥ 30 ng/mL) status. Novel findings demonstrate low vitamin D correlates with higher SSNHL onset/recurrence, particularly elevating risk in ...
Qi Hui   +8 more
wiley   +1 more source

Therapeutic Plasma Exchange and Changes in Calcium, Phosphate, Parathyroid Hormone, and Fibroblast Growth Factor-23.

open access: yesJ Clin Endocrinol Metab
Jin SS   +6 more
europepmc   +1 more source

The effects of parathyroid hormone, alendronate, or both in men with osteoporosis.

open access: yesNew England Journal of Medicine, 2003
J. Finkelstein   +5 more
semanticscholar   +1 more source

24R,25(OH)2D3 regulates tumorigenesis in estrogen sensitive laryngeal cancer cells via membrane‐associated receptor complexes in ER+ and ER− cells

open access: yesInternational Journal of Cancer, Volume 158, Issue 1, Page 202-217, 1 January 2026.
What's new? Estrogen receptors likely influence the development of laryngeal cancer and are of particular interest in regard to their relationship with the vitamin D metabolite 24R,25(OH)2D3. In this study the authors examined interactions between 24R,25(OH)2D3 and estrogen‐responsive laryngeal tumorigenesis.
Cydney D. Dennis   +10 more
wiley   +1 more source

Pheochromocytoma and Diffuse Large B‐Cell Lymphoma in the Ipsilateral Adrenal Gland: A Case Report

open access: yesIJU Case Reports, Volume 9, Issue 1, January 2026.
ABSTRACT Introduction Pheochromocytoma is a catecholamine‐producing tumor arising from the adrenal medulla. When it coexists with a tumor of different origin within the same adrenal gland, it is classified as a collision tumor involving a pheochromocytoma.
Ken Maekawa   +9 more
wiley   +1 more source

PTHrP‐Producing Renal Cell Carcinoma Presenting as Rapidly Progressive Cognitive Impairment: A Case Report

open access: yesIJU Case Reports, Volume 9, Issue 1, January 2026.
ABSTRACT Introduction Humoral hypercalcemia of malignancy (HCM) caused by parathyroid hormone–related peptide (PTHrP) is a common paraneoplastic syndrome, and renal cell carcinoma (RCC) is one of the main causes. However, initial presentation with rapidly progressive cognitive decline is rare.
Fumiakira Yano   +6 more
wiley   +1 more source

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