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Journal Abstract Search

298 related items for PubMed ID: 7637271

  • 1. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
    Praga M, Vara J, González-Parra E, Andrés A, Alamo C, Araque A, Ortiz A, Rodicio JL.
    Kidney Int; 1995 May; 47(5):1419-25. PubMed ID: 7637271
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  • 2. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
    Kari JA, Farouq M, Alshaya HO.
    Pediatr Nephrol; 2003 Jun; 18(6):506-10. PubMed ID: 12720080
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  • 3. Familial hypomagnesemia-hypercalciuria in 2 siblings.
    Kuwertz-Bröking E, Fründ S, Bulla M, Kleta R, August C, Kisters K.
    Clin Nephrol; 2001 Aug; 56(2):155-61. PubMed ID: 11522093
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  • 8. 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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  • 12. A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings.
    Alparslan C, Öncel EP, Akbay S, Alaygut D, Mutlubaş F, Tatlı M, Konrad M, Yavaşcan Ö, Kasap-Demir B.
    Turk J Pediatr; 2018 Aug; 60(1):76-80. PubMed ID: 30102483
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  • 13. 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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  • 14. Claudin-19 mutations and clinical phenotype in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
    Claverie-Martín F, García-Nieto V, Loris C, Ariceta G, Nadal I, Espinosa L, Fernández-Maseda Á, Antón-Gamero M, Avila A, Madrid Á, González-Acosta H, Córdoba-Lanus E, Santos F, Gil-Calvo M, Espino M, García-Martinez E, Sanchez A, Muley R, RenalTube Group.
    PLoS One; 2013 Jul 13; 8(1):e53151. PubMed ID: 23301036
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  • 16. Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
    Weber S, Schneider L, Peters M, Misselwitz J, Rönnefarth G, Böswald M, Bonzel KE, Seeman T, Suláková T, Kuwertz-Bröking E, Gregoric A, Palcoux JB, Tasic V, Manz F, Schärer K, Seyberth HW, Konrad M.
    J Am Soc Nephrol; 2001 Sep 13; 12(9):1872-1881. PubMed ID: 11518780
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  • 17. An unusual patient with hypercalciuria, recurrent nephrolithiasis, hypomagnesemia and G227R mutation of Paracellin-1. An unusual patient with hypercalciuria and hypomagnesemia unresponsive to thiazide diuretics.
    Kutluturk F, Temel B, Uslu B, Aral F, Azezli A, Orhan Y, Konrad M, Ozbey N.
    Horm Res; 2006 Sep 13; 66(4):175-81. PubMed ID: 16804318
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  • 19. Hypomagnesaemia-hypercalciuria-nephrocalcinosis: a report of nine cases and a review.
    Benigno V, Canonica CS, Bettinelli A, von Vigier RO, Truttmann AC, Bianchetti MG.
    Nephrol Dial Transplant; 2000 May 13; 15(5):605-10. PubMed ID: 10809799
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