Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Hypercalciuria and SLC34A3[original query] |
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| Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis. Journal of the American Society of Nephrology : JASN 2014 Oct 25 (10): 2366-75. Dasgupta Debayan, Wee Mark J, Reyes Monica, Li Yuwen, Simm Peter J, Sharma Amita, Schlingmann Karl-Peter, Janner Marco, Biggin Andrew, Lazier Joanna, Gessner Michaela, Chrysis Dionisios, Tuchman Shamir, Baluarte H Jorge, Levine Michael A, Tiosano Dov, Insogna Karl, Hanley David A, Carpenter Thomas O, Ichikawa Shoji, Hoppe Bernd, Konrad Martin, Sävendahl Lars, Munns Craig F, Lee Hang, Jüppner Harald, Bergwitz Cleme |
| Renal phosphate handling and inherited disorders of phosphate reabsorption: an update. Pediatric nephrology (Berlin, Germany) 2017 12 34 (4): 549-559. Wagner Carsten A, Rubio-Aliaga Isabel, Hernando Na |
| SLC34A3 Intronic Deletion in an Iranian Kindred with Hereditary Hypophosphatemic Rickets with Hypercalciuria. Journal of clinical research in pediatric endocrinology 2018 5 10 (4): 343-349. Hasani-Ranjbar Shirin, Ejtahed Hanieh-Sadat, Amoli Mahsa M., Bitarafan Fatemeh, Qorbani Mostafa, Soltani Akbar, Yarjoo Bahar |
| 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, 2023
- Page last updated:Sep 29, 2023
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