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Journal Abstract Search

201 related items for PubMed ID: 16886568

  • 1. [The diagnosis of familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a girl with acute lymphoblastic leukemia--case report].
    Sikora P, Borzecka H, Kołłataj B, Majewski M, Wieczorkiewicz-Płaza A, Zajaczkowska M.
    Pol Merkur Lekarski; 2006 Apr; 20(118):430-2. PubMed ID: 16886568
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  • 2. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis in 2 sisters.
    Al-Elq AH.
    Saudi Med J; 2008 Mar; 29(3):447-51. PubMed ID: 18327378
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  • 10. Hypomagnesemia-hypercalciuria-nephrocalcinosis and ocular findings: a new claudin-19 mutation.
    Ekinci Z, Karabaş L, Konrad M.
    Turk J Pediatr; 2012 Mar; 54(2):168-70. PubMed ID: 22734304
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  • 13. [Familial hypomagnesemia, hypercalciuria with nephrocalcinosis syndrome: report of a case].
    Alvarez Ponte SB, López M, Golinelli F, D'Angelo S, Martin S.
    Arch Argent Pediatr; 2011 Feb; 109(1):8-12. PubMed ID: 21283935
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  • 15. 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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  • 17. 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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  • 18. Familial hypomagnesemia-hypercalciuria in 2 siblings.
    Kuwertz-Bröking E, Fründ S, Bulla M, Kleta R, August C, Kisters K.
    Clin Nephrol; 2001 Aug 01; 56(2):155-61. PubMed ID: 11522093
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  • 19. Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene.
    Weber S, Hoffmann K, Jeck N, Saar K, Boeswald M, Kuwertz-Broeking E, Meij II, Knoers NV, Cochat P, Suláková T, Bonzel KE, Soergel M, Manz F, Schaerer K, Seyberth HW, Reis A, Konrad M.
    Eur J Hum Genet; 2000 Jun 01; 8(6):414-22. PubMed ID: 10878661
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