نتایج جستجو برای: idiopathic hypercalciuria

تعداد نتایج: 63884  

2010
Natalia Mejia-Gaviria Helena Gil-Peña Eliecer Coto Teresa M Pérez-Menéndez Fernando Santos

Hereditary hypophosphatemic rickets with hypercalciuria is a rare autosomal recessive disorder (OMIM #241530), characterized by decreased renal phosphate reabsorption that leads to hypophosphatemia, rickets, and bone pain; hypophosphatemia is believed to stimulate 1,25 dihydroxyvitamin D synthesis which, in turn, results in hypercalciuria. Hereditary hypophosphatemic rickets with hypercalciuria...

Journal: :The Tokai journal of experimental and clinical medicine 1987
K Matsushita K Tanikawa

Thirty-six patients with recurrent calcium oxalate nephrolithiasis were selected from the stone clinic. Fourteen were normocalcemic and had normal daily urinary calcium excretion. Among 22 patients with idiopathic hypercalciuria, 10 received thiazide diuretics for the prevention of new stone formation. Single-voided urine samples were collected at the outpatient clinic and 24-hour urine at the ...

Journal: :Acta pharmaceutica 2016
Miroslav Zeman Marek Vecka František Perlík Barbora Staňková Robert Hromádka Eva Tvrzická Jakub Širc Jakub Hrib Aleš Žák

Niacin was the first hypolipidemic drug to significantly reduce both major cardiovascular events and mortality in patients with cardiovascular disease. Niacin favorably influences all lipoprotein classes, including lipoprotein[a],and belongs to the most potent hypolipidemic drugs for increasing HDL-C. Moreover, niacin causes favorable changes to the qualitative composition of lipoprotein HDL. I...

2017
Pilar Peris Bernal

Although there are some differential aspects related to peak bone mass acquisition and later bone loss throughout life between genders, the frequency of osteoporosis in young individuals is similar for both genders. In addition, in this population group, the development of osteoporosis is frequently associated with secondary causes. Indeed, nearly 50% of young individuals with osteoporosis have...

Journal: :American journal of physiology. Renal physiology 2013
Kevin K Frick John R Asplin Nancy S Krieger Christopher D Culbertson Daniel M Asplin David A Bushinsky

The inbred genetic hypercalciuric stone-forming (GHS) rats exhibit many features of human idiopathic hypercalciuria and have elevated levels of vitamin D receptors (VDR) in calcium (Ca)-transporting organs. On a normal-Ca diet, 1,25(OH)2D3 (1,25D) increases urine (U) Ca to a greater extent in GHS than in controls [Sprague-Dawley (SD)]. The additional UCa may result from an increase in intestina...

Journal: :Reumatologia clinica 2010
Pilar Peris Bernal

Although there are some differential aspects related to peak bone mass acquisition and later bone loss throughout life between genders, the frequency of osteoporosis in young individuals is similar for both genders. In addition, in this population group, the development of osteoporosis is frequently associated with secondary causes. Indeed, nearly 50% of young individuals with osteoporosis have...

2013
Nellie Y. Loh Liz Bentley Henrik Dimke Sjoerd Verkaart Paolo Tammaro Caroline M. Gorvin Michael J. Stechman Bushra N. Ahmad Fadil M. Hannan Sian E. Piret Holly Evans Ilaria Bellantuono Tertius A. Hough William D. Fraser Joost G. J. Hoenderop Frances M. Ashcroft Steve D. M. Brown René J. M. Bindels Roger D. Cox Rajesh V. Thakker

Hypercalciuria is a major cause of nephrolithiasis, and is a common and complex disorder involving genetic and environmental factors. Identification of genetic factors for monogenic forms of hypercalciuria is hampered by the limited availability of large families, and to facilitate such studies, we screened for hypercalciuria in mice from an N-ethyl-N-nitrosourea mutagenesis programme. We ident...

2017
Emma Davidson Peiris Raghav Wusirika

CYP24A1 is an enzyme that inactivates vitamin D. Loss-of-function mutations in this enzyme are rare but have been linked with idiopathic infantile hypercalcemia as well as adult-onset nephrocalcinosis and nephrolithiasis. Genetic testing for this mutation should be considered in the presence of calciuria, elevated serum calcium, elevated 1,25-dihydroxyvitamin D, and suppressed parathyroid hormo...

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