Results 31 to 40 of about 11,294 (209)

Association of hypercalciuria with vitamin D supplementation in patients undergoing ketogenic dietary therapy

Frontiers in Nutrition, 2022
BackgroundKetogenic dietary therapy (KDT) is used as an effective treatment for epilepsy. However, KDT carries the risk of bone health deterioration; therefore, vitamin D supplementation is required.
Myeongseob Lee, Hae In Lee, Kyungchul Song, Han Saem Choi, Junghwan Suh, Se Hee Kim, Hyun Wook Chae, Hoon-Chul Kang, Joon Soo Lee, Heung Dong Kim, Ho-Seong Kim, Ahreum Kwon   +11 more
doaj   +1 more source

Empagliflozin does not prevent progression of Dent's disease type 1 in a mouse model

Experimental Physiology, Volume 111, Issue 2, Page 517-526, 1 February 2026.
Abstract Dent's disease is a rare inherited renal disorder characterized by generalized proximal tubule dysfunction with low molecular weight proteinuria, hypercalciuria, and urinary loss of other solutes. The disease is progressive and leads to chronic kidney disease.
Elise de Combiens, Nadia Frachon, Yohan Bignon, Marc Fila, Clément Brossard, Perrine Frère, Stéphane Lourdel   +6 more
wiley   +1 more source

Hypercalcemia, hypercalciuria and nephrocalcinosis in a breast-fed term newborn: A rare presentation

Saudi Journal of Kidney Diseases and Transplantation, 2014
Although hypercalcemia and hypercalciuria are known to occur in breast-fed pre-term infants, to the best of our knowledge, it has never been reported in a term baby previously.
Issa A Hazza, Manahil S Ghandour, Reham I Almardini, Rana E Haddad, Ghazi M Salaita   +4 more
doaj   +1 more source

Computerized tomography‐derived body composition metrics are associated with 24‐h urine lithogenic parameters

BJUI Compass, Volume 7, Issue 1, January 2026.
Abstract Background The relationship between body composition and lithogenic urine parameters remains poorly defined. This study aimed to evaluate associations between computerized tomography (CT)‐derived body composition metrics and 24‐h urine findings. Methods Stone‐forming patients in our Nephrolithiasis Database who underwent 24‐h urine testing and
Reza Lahiji, Lorenzo Storino Ramacciotti, Ernie Morton, Edouard H. Nicaise, Adam Braunschweig, Gregory Palmateer, Benjamin Schmeusser, Dattatraya Patil, Maxwell Richardson, Frank Glover, Ethan Kearns, Aaron Lay, Mohammad Hajiha, Viraj A. Master, Kenneth Ogan   +14 more
wiley   +1 more source

Defining hypercalciuria in nephrolithiasis [PDF]

Kidney International, 2011
The classic definition of hypercalciuria, an upper normal limit of 200  mg/day, is based on a constant diet restricted in calcium, sodium, and animal protein; however, random diet data challenge this. Here our retrospective study determined the validity of the classic definition of hypercalciuria by comparing data from 39 publications analyzing urinary
Charles Y C, Pak, Khashayar, Sakhaee, Orson W, Moe, John, Poindexter, Beverley, Adams-Huet, Margaret S, Pearle, Joseph E, Zerwekh, Glenn M, Preminger, Michael R, Wills, Neil A, Breslau, Fredric C, Bartter, D C, Brater, Howard J, Heller, Clarita V, Odvina, Cindy L, Wabner, John S, Fordtran, Man, Oh, Abhimanyu, Garg, Jean A, Harvey, Robert J, Alpern, William H, Snyder, Paul C, Peters   +21 more
openaire   +2 more sources

Antiurolithiatic Potential of a Series of Phthalimide Derivatives on Calcium Oxalate Crystals

Chemistry &Biodiversity, Volume 23, Issue 1, January 2026.
ABSTRACT Urolithiasis, primarily caused by calcium oxalate crystals, represents a major health concern due to high recurrence rates and limitations of current treatments in dissolving existing stones. This study investigated the antiurolithiatic potential of 15 phthalimide derivatives against calcium oxalate monohydrate (COM) and dihydrate (COD ...
Daniele Regina Sonza, Laura Von Borell du Vernay França, Rita de Cássia Vilhena da Silva, Anelize Dada, Mariana Zanovello, Thaise Boeing, Priscila de Souza, Rogério Correa   +7 more
wiley   +1 more source

Vitamin D receptor gene polymorphisms in children with kidney stone disease

The Turkish Journal of Pediatrics, 2017
Kidney stone disease has a multifactorial etiology involving the interaction of genetic and environmental factors. There is an increased risk of stone formation in the relatives of idiopathic stone patients, which can be explained up to 60% by genetic ...
Berivan Subaşı, İbrahim Gökçe, Kenan Delil, Harika Alpay   +3 more
doaj   +1 more source

a novel variant of gene in a neonate with congenital hypoparathyroidism [PDF]

Annals of Pediatric Endocrinology & Metabolism, 2018
Autosomal-dominant hypocalcemia with hypercalciuria (ADHH) is a genetic disease characterized by hypoparathyroidism with hypercalciuria. Most patients with ADHH have calcium-sensing receptor (CaSR) gene mutations.
Jung-Eun Moon, Su-Jeong Lee, Suk-Hyun Park, Jinsup Kim, Dong-Kyu Jin, Cheol Woo Ko   +5 more
doaj   +1 more source

Relationship between Urinary Calcium Excretion and Lower Urinary Tract Symptoms

Metabolites, 2022
To date, few detailed studies have been conducted on the convenient and useful markers for the prevalence of lower urinary tract symptoms (LUTS), including overactive bladder (OAB) and nocturia.
Tomohiro Matsuo, Hidenori Ito, Kensuke Mitsunari, Kojiro Ohba, Yasuyoshi Miyata   +4 more
doaj   +1 more source

A Giant Parathyroid Adenoma Presenting as Coughs and Dyspnea in a Young Woman: A Case Report

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT A parathyroid adenoma is defined as a benign tumor in the parathyroid glands. A type of parathyroid adenoma is giant parathyroid adenoma that weighs > 3.5 g and has a size of more than 2 cm. A 37‐year‐old woman presented with coughs and dyspnea without fever, hemoptysis, and weight loss. Examination of the patient revealed a diffusely enlarged
Somayeh Chahkandi, Nasrin Amiri‐Dashatan, Mehdi Koushki, Mojgan Sanjari   +3 more
wiley   +1 more source