Human Genome Epidemiology Literature Finder
|
Records 1 - 5 (of 5 Records) |
| Query Trace: Nephrocalcinosis and PTH[original query] |
|---|
| Mutational Spectrum of CYP24A1 Gene in a Cohort of Italian Patients with Idiopathic Infantile Hypercalcemia. Nephron 2016 Jul 133 (3): . Gigante Maddalena, Santangelo Luisa, Diella Sterpeta, Caridi Gianluca, Argentiero Lucia, D'Alessandro Maria Michela, Martino Marida, Stea Emma Diletta, Ardissino Gianluigi, Carbone Vincenza, Pepe Silvana, Scrutinio Domenico, Maringhini Silvio, Ghiggeri Gian Marco, Grandaliano Giuseppe, Giordano Mario, Gesualdo Lore |
| Therapy with PTH 1-34 or calcitriol and calcium in diverse etiologies of hypoparathyroidism over 27 years at a single tertiary care center. Bone 2021 5 149 115977. Winer Karen K, Ye Shangyuan, Ferré Elise M N, Schmitt Monica M, Zhang Bo, Cutler Gordon B, Lionakis Michail |
| Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations. Journal of nephrology 2021 4 34 (6): 2053-2062. Vall-Palomar Mònica, Burballa Carla, Claverie-Martín Félix, Meseguer Anna, Ariceta Ge |
| Overlapping Phenotypes Associated With CYP24A1, SLC34A1, and SLC34A3 Mutations: A Cohort Study of Patients With Hypersensitivity to Vitamin D. Frontiers in endocrinology 2021 11 12 736240. Molin Arnaud, Lemoine Sandrine, Kaufmann Martin, Breton Pierre, Nowoczyn Marie, Ballandonne Céline, Coudray Nadia, Mittre Hervé, Richard Nicolas, Ryckwaert Amélie, Lavillaureix Alinoe, Jones Glenville, Bacchetta Justine, Kottler Marie-Lau |
| Idiopathic infantile hypercalcemia in children with chronic kidney disease due to kidney hypodysplasia. Pediatric nephrology (Berlin, Germany) 2022 9 38 (4): 1067-1073. Gurevich Evgenia, Borovitz Yael, Levi Shelli, Perlman Sharon, Landau Dani |
- Page last reviewed:Feb 1, 2024
- Content source: