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Journal Abstract Search

176 related items for PubMed ID: 24924704

  • 61. Mild Idiopathic Infantile Hypercalcemia-Part 1: Biochemical and Genetic Findings.
    Lenherr-Taube N, Young EJ, Furman M, Elia Y, Assor E, Chitayat D, Uster T, Kirwin S, Robbins K, Vinette KMB, Daneman A, Marshall CR, Collins C, Thummel K, Sochett E, Levine MA.
    J Clin Endocrinol Metab; 2021 Sep 27; 106(10):2915-2937. PubMed ID: 34125233
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  • 62. A girl with rickets and nephrocalcinosis.
    Godefroid N, Proesmans W.
    Pediatr Nephrol; 2003 Jun 27; 18(6):573-5. PubMed ID: 12720081
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  • 63. A novel CLDN16 mutation in familial hypomagnesemia with hypercalciuria and nephrocalcinosis
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    Zhang H, Ling C, Liu X.
    Clin Nephrol; 2019 Aug 27; 92(2):95-97. PubMed ID: 31232269
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  • 65. Hereditary hypophosphatemia in Norway: a retrospective population-based study of genotypes, phenotypes, and treatment complications.
    Rafaelsen S, Johansson S, Ræder H, Bjerknes R.
    Eur J Endocrinol; 2016 Feb 27; 174(2):125-36. PubMed ID: 26543054
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  • 67. Fluconazole in hypercalciuric patients with increased 1,25(OH)2D levels: the prospective, randomized, placebo-controlled, double-blind FLUCOLITH trial.
    Bertholet-Thomas A, Portefaix A, Flammier S, Dhelens C, Subtil F, Dubourg L, Laudy V, Le Bouar M, Boussaha I, Ndiaye M, Molin A, Lemoine S, Bacchetta J.
    Trials; 2022 Jun 16; 23(1):499. PubMed ID: 35710560
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  • 68. Characterization of two novel mutations in the claudin-16 and claudin-19 genes that cause familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
    Perdomo-Ramirez A, Aguirre M, Davitaia T, Ariceta G, Ramos-Trujillo E, RenalTube Group, Claverie-Martin F.
    Gene; 2019 Mar 20; 689():227-234. PubMed ID: 30576809
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  • 69. Hereditary hypophosphatemic rickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene.
    Jones AO, Tzenova J, Frappier D, Crumley MJ, Roslin NM, Kos CH, Tieder M, Langman CB, Proesmans W, Carpenter TO, Rice A, Anderson D, Morgan K, Fujiwara TM, Tenenhouse HS.
    J Am Soc Nephrol; 2001 Mar 20; 12(3):507-514. PubMed ID: 11181798
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  • 70. Phosphate transport: molecular basis, regulation and pathophysiology.
    Tenenhouse HS.
    J Steroid Biochem Mol Biol; 2007 Mar 20; 103(3-5):572-7. PubMed ID: 17270430
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  • 73. Mutational analysis of PHEX, FGF23, DMP1, SLC34A3 and CLCN5 in patients with hypophosphatemic rickets.
    Beck-Nielsen SS, Brixen K, Gram J, Brusgaard K.
    J Hum Genet; 2012 Jul 20; 57(7):453-8. PubMed ID: 22695891
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  • 74. Hereditary hypophosphatemic rickets with hypercalciuria.
    Tieder M, Modai D, Samuel R, Arie R, Halabe A, Bab I, Gabizon D, Liberman UA.
    N Engl J Med; 1985 Mar 07; 312(10):611-7. PubMed ID: 2983203
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  • 78. Hypomagnesemia and nephrocalcinosis in a patient with two heterozygous mutations in the CLDN16 gene.
    Staiger K, Staiger H, Haas C, Thamer C, Risler T, Machicao F, Häring HU.
    J Nephrol; 2007 Mar 07; 20(1):107-10. PubMed ID: 17347984
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  • 79. A single case of hypophosphatemic rickets with hypercalciuria.
    Nishiyama S, Inoue F, Matsuda I.
    J Pediatr Gastroenterol Nutr; 1986 Mar 07; 5(5):826-9. PubMed ID: 3761117
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