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Journal Abstract Search

224 related items for PubMed ID: 24321194

  • 1. A novel CLDN16 mutation in a large family with familial hypomagnesaemia with hypercalciuria and nephrocalcinosis.
    Deeb A, Abood SA, Simon J, Dastoor H, Pearce SH, Sayer JA.
    BMC Res Notes; 2013 Dec 10; 6():527. PubMed ID: 24321194
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  • 2. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: report of three Turkish siblings.
    Peru H, Akin F, Elmas S, Elmaci AM, Konrad M.
    Pediatr Nephrol; 2008 Jun 10; 23(6):1009-12. PubMed ID: 18253757
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  • 5. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family.
    Al-Haggar M, Bakr A, Tajima T, Fujieda K, Hammad A, Soliman O, Darwish A, Al-Said A, Yahia S, Abdel-Hady D.
    Clin Exp Nephrol; 2009 Aug 10; 13(4):288-294. PubMed ID: 19165416
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  • 6. 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 10; 92(2):95-97. PubMed ID: 31232269
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  • 10. A novel mutation in CLDN16 results in rare familial hypomagnesaemia with hypercalciuria and nephrocalcinosis in a Chinese family.
    Lv F, Xu XJ, Wang JY, Liu Y, Jiang Y, Wang O, Xia WB, Xing XP, Li M.
    Clin Chim Acta; 2016 Jun 01; 457():69-74. PubMed ID: 27067446
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  • 12. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: variable phenotypic expression in three affected sisters from Mexican ancestry.
    Arteaga ME, Hunziker W, Teo AS, Hillmer AM, Mutchinick OM.
    Ren Fail; 2015 Feb 01; 37(1):180-3. PubMed ID: 25366522
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  • 13. Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (FHHNC): compound heterozygous mutation in the claudin 16 (CLDN16) gene.
    Hampson G, Konrad MA, Scoble J.
    BMC Nephrol; 2008 Sep 24; 9():12. PubMed ID: 18816383
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  • 14. Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a delayed diagnosis: a case report.
    Lu J, Zhao X, Paiardini A, Lang Y, Bottillo I, Shao L.
    BMC Nephrol; 2018 Jul 13; 19(1):181. PubMed ID: 30005619
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  • 15. Claudin 19-based familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a sibling pair.
    Sharma S, Place E, Lord K, Leroy BP, Falk MJ, Pradhan M.
    Clin Nephrol; 2016 Jun 13; 85(6):346-52. PubMed ID: 27007868
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  • 16. Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis: the first four patients in Serbia.
    Peco-Antić A, Konrad M, Milosevski-Lomić G, Dimitrijević N.
    Srp Arh Celok Lek; 2010 Jun 13; 138(5-6):351-5. PubMed ID: 20607983
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  • 19. Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
    García-Castaño A, Perdomo-Ramirez A, Vall-Palomar M, Ramos-Trujillo E, Madariaga L, Ariceta G, Claverie-Martin F.
    Mol Genet Genomic Med; 2020 Nov 13; 8(11):e1475. PubMed ID: 32869508
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