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Journal Abstract Search

260 related items for PubMed ID: 30102483

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  • 2. First report of a novel missense CLDN19 mutations causing familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a Chinese family.
    Yuan T, Pang Q, Xing X, Wang X, Li Y, Li J, Wu X, Li M, Wang O, Jiang Y, Dong J, Xia W.
    Calcif Tissue Int; 2015 Apr; 96(4):265-73. PubMed ID: 25555744
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  • 4. 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; 13(4):288-294. PubMed ID: 19165416
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  • 8. 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; 85(6):346-52. PubMed ID: 27007868
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  • 9. Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features.
    Eltan M, Yavas Abali Z, Turkyilmaz A, Gokce I, Abali S, Alavanda C, Arman A, Kirkgoz T, Guran T, Hatun S, Bereket A, Turan S.
    Calcif Tissue Int; 2022 Apr; 110(4):441-450. PubMed ID: 34761296
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  • 10. Identification of the first large deletion in the CLDN16 gene in a patient with FHHNC and late-onset of chronic kidney disease: case report.
    Yamaguti PM, dos Santos PA, Leal BS, Santana VB, Mazzeu JF, Acevedo AC, Neves Fde A.
    BMC Nephrol; 2015 Jul 02; 16():92. PubMed ID: 26136118
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  • 17. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis in 2 sisters.
    Al-Elq AH.
    Saudi Med J; 2008 Mar 02; 29(3):447-51. PubMed ID: 18327378
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