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Journal Abstract Search

194 related items for PubMed ID: 21283935

  • 1. [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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  • 2. Three different causes of hypercalciuria.
    Skalova S, Konrad M, Kutilek S.
    Klin Padiatr; 2011 Sep; 223(5):287-9. PubMed ID: 21698557
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  • 3. A novel mutation of the claudin 16 gene in familial hypomagnesemia with hypercalciuria and nephrocalcinosis mimicking rickets.
    Kasapkara CS, Tumer L, Okur I, Hasanoglu A.
    Genet Couns; 2011 Sep; 22(2):187-92. PubMed ID: 21848011
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  • 10. 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; 37(1):180-3. PubMed ID: 25366522
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  • 11. Nephrocalcinosis in siblings--familial hypomagnesemia, hypercalciuria with nephrocalcinosis (FHHNC syndrome).
    Prabahar MR, Manorajan R, Fernando ME, Venkatraman R, Balaraman V, Jayakumar M.
    J Assoc Physicians India; 2006 Jun; 54():497-500. PubMed ID: 16909703
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  • 12. [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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  • 13. Hypomagnesemia-hypercalciuria-nephrocalcinosis and ocular findings: a new claudin-19 mutation.
    Ekinci Z, Karabaş L, Konrad M.
    Turk J Pediatr; 2012 Apr; 54(2):168-70. PubMed ID: 22734304
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