Results 71 to 80 of about 17,098 (226)

Metabolic diagnosis and medical prevention of calcium nephrolithiasis and its systemic manifestations: a consensus statement [PDF]

, 2016
Background: Recently published guidelines on the medical management of renal stone disease did not address relevant topics in the field of idiopathic calcium nephrolithiasis, which are important also for clinical research.
Bartoletti, R., Buchholz, N., Buchholz, N.N.-P. (Noor), Bushinsky, D., Bushinsky, D. (David), Capasso, G.B., Cicerello, E., Coe, F., Coe, F. (Fredric), Croppi, E. (Emanuele), Cupisti, A., Curhan, G.C., Curhan, G.C. (Gary C.), Desai, J., Fabris, A., Ferraro, P.M., Ferraro, P.M. (Pietro Manuel), Fuster, D., Fuster, D. (Daniel), Gambaro, G., Gambaro, G. (Giovanni), Goldfarb, D.S., Goldfarb, D.S. (David S.), Heilberg, I.P., Heilberg, I.P. (Ita Pfeferman), Hess, B., Hess, B. (Bernhard), Jaeger, P. (Ph), Kirkali, Z. (Ziya), Kok, D.J. (Dirk), Letavernier, E., Lieske, J., Lieske, J. (John), Lingeman, J., Lingeman, J. (James), Marangella, M., Marangella, M. (Martino), Mazzaferro, S., Milliner, D., Milliner, D. (Dawn), Moe, O., Moe, O. (Orson), Nouvenne, A., Preminger, G.M., Preminger, G.M. (Glen M.), Prie, D., Reis Santos, J., Reis Santos, J.M. (Jose’ Manuel), Rendina, D., Sakhaee, K. (Khashayar), Sarica, K., Sarica, K. (Kemal), Siener, R., Siener, R. (Roswitha), Soldati, L., Strazzullo, P., Strazzullo, P. (Pasquale), Tasca, A., Trinchieri, A., Vezzoli, G., Vitale, C., Williams, J.C., Williams, J.C. (James C.), Worcester, E., Worcester, E. (Elen), Wu, W.   +65 more
core   +3 more sources

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

Gitelman Syndrome Presenting With Syncope and Treatment‐Refractory Hypokalemia in A Young Woman: A Case Report

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Gitelman syndrome (GS) is a rare autosomal recessive tubulopathy characterized by hypokalemic metabolic alkalosis, hypomagnesemia, and hypocalciuria. A 27‐year‐old woman presented with a witnessed syncopal episode, progressive weakness, and nausea.
Iyassu S. Melkie, Abenezer A. Wolde, Lulit Y. Mengesha, Rahwa A. Kinfe, Chernet T. Mengistie, Zenebwork Y. Gubai   +5 more
wiley   +1 more source

Urolithiasis and Osteoporosis: Clinical Relevance and Therapeutic Implications [PDF]

, 2009
Several clinical and epidemiological studies revealed increased bone turnover and lower bone mass in patients with urolithiasis. Bone mass loss is particularly evident in idiopathic calcium stone formers.
Ines Bilić-Ćurčić, Ivan Mihaljević, Jasminka Milas-Ahić, Martina Smolić, Robert Smolić, Sandra Tucak-Zorić   +5 more
core   +1 more source

Screening of hypercalciuria among children with persistent asymptomatic hematuria

Journal of Biostatistics and Epidemiology, 2018
Background & Aim: Hypercalciuria is commonly observed in accompany with some conditions. Hypercalciuria can clinically present different symptoms and signs. The diagnostic methods for hypercalciuria have not yet been standardized. The presented study was
Mohsen Akhavansepahi, Bibi Leila hoseini, Yaser Tabarai   +2 more
doaj  

Metabolic evaluation in patients with nephrolithiasis: A report from Isfahan, Iran

Advanced Biomedical Research, 2012
Background: Nephrolithiasis is a major public health problem worldwide. In recent years, growing evidence suggest that this disease may originate from underlying metabolic disorders.
Afsoon Emami-Naini, Amid Eshraghi, Shahrzad Shahidi, Mojgan Mortazavi, Shiva Seyrafian, Peyman Roomizadeh, Seyed-Hossein Abtahi, Hamed-Basir Ghafoori   +7 more
doaj   +1 more source

Rare Neurosarcoidosis Involvements

Respirology Case Reports, Volume 14, Issue 3, March 2026.
Neurosarcoidosis is a rare manifestation of systemic sarcoidosis. Establishing a diagnosis can be challenging for clinicians, particularly in cases of isolated neurosarcoidosis. Here, we present nine patients with rare manifestations of neurosarcoidosis. ABSTRACT Neurosarcoidosis is a rare manifestation of systemic sarcoidosis. Establishing a diagnosis
Gülce Cansu Serin, Serhat Erol, Gökhan Çelik, Özlem Özdemir Kumbasar   +3 more
wiley   +1 more source

PTH and 1.25 vitamin D response to a low-calcium diet is associated with bone mineral density in renal stone formers [PDF]

, 2017
Background. Renal calcium stones and hypercalciuria are associated with a reduced bone mineral density (BMD). Therefore, the effect of changes in calcium homeostasis is of interest for both stones and bones. We hypothesized that the response of calciuria,
Bonny, Olivier, Eisenberger, Ute, Frey, Felix J., Mohaupt, Markus G., Pasch, Andreas   +4 more
core  

Ketogenic diet-induced weight loss is associated with an increase in vitamin d levels in obese adults [PDF]

, 2019
Vitamin D is an important micronutrient involved in several processes. Evidence has shown a strong association between hypovitaminosis D and cardio-metabolic diseases, including obesity.
Gigliotti, S, Maio, R, Perticone, F., Perticone, M, Pinto, A, Pujia, R, Sciacqua, A, Sesti, G, Suraci, E, Zito, R   +9 more
core   +1 more source

The urinary calcium–magnesium product as a potential indicator of nephrolithiasis in primary hyperparathyroidism

Endokrynologia Polska
INTRODUCTION: Nephrolithiasis is a common complication of primary hyperparathyroidism (PHPT), but the mechanisms underlying stone formation remain incompletely understood.
Michał Popow, Sebastian Szewczyk, Janusz Sierdziński, Małgorzata Bobrowicz, Urszula Ambroziak   +4 more
doaj   +1 more source