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Journal Abstract Search

219 related items for PubMed ID: 12720080

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  • 3. 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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  • 6. Two heterozygous mutations of CLDN16 in a Japanese patient with FHHNC.
    Tajima T, Nakae J, Fujieda K.
    Pediatr Nephrol; 2003 Dec; 18(12):1280-2. PubMed ID: 14586675
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  • 8. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations.
    Kang JH, Choi HJ, Cho HY, Lee JH, Ha IS, Cheong HI, Choi Y.
    Pediatr Nephrol; 2005 Oct; 20(10):1490-3. PubMed ID: 16047219
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  • 12. A novel PCLN-1 gene mutation in familial hypomagnesemia with hypercalciuria and atypical phenotype.
    Sanjad SA, Hariri A, Habbal ZM, Lifton RP.
    Pediatr Nephrol; 2007 Apr; 22(4):503-8. PubMed ID: 17123117
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  • 13. 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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  • 15. Inherited hypercalciuric syndromes: Dent's disease (CLC-5) and familial hypomagnesemia with hypercalciuria (paracellin-1).
    Knohl SJ, Scheinman SJ.
    Semin Nephrol; 2004 Jan; 24(1):55-60. PubMed ID: 14730510
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  • 16. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
    Vall-Palomar M, Madariaga L, Ariceta G.
    Pediatr Nephrol; 2021 Oct; 36(10):3045-3055. PubMed ID: 33595712
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  • 17. Hypomagnesemia with hypercalciuria and nephrocalcinosis: case report and a family study.
    Tasic V, Dervisov D, Koceva S, Weber S, Konrad M.
    Pediatr Nephrol; 2005 Jul; 20(7):1003-6. PubMed ID: 15856319
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  • 18. 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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  • 19. Hypomagnesemia-hypercalciuria-nephrocalcinosis and ocular findings: a new claudin-19 mutation.
    Ekinci Z, Karabaş L, Konrad M.
    Turk J Pediatr; 2012 Jul 13; 54(2):168-70. PubMed ID: 22734304
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