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Journal Abstract Search

268 related items for PubMed ID: 15503623

  • 1. Familial hypomagnesemia--hypercalciuria and pseudotumor cerebri.
    Gregoric A, Bracic K, Marcun-Varda N.
    Wien Klin Wochenschr; 2001; 113 Suppl 3():59-61. PubMed ID: 15503623
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  • 2. 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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  • 3. Pseudotumor cerebri in a child with familial hypomagnesemia-hypercalciuria.
    Gregoric A, Bracic K, Novljan G, Marcun-Varda N.
    Pediatr Nephrol; 2000 Mar; 14(3):269-70. PubMed ID: 10752769
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  • 6. 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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  • 8. 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 May; 66(4):175-81. PubMed ID: 16804318
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  • 10. Renal hypomagnesemia, hypercalciuria and nephrocalcinosis in a middle-aged man.
    Enríquez R, Sirvent AE, Amorós F, Martínez M, Cabezuelo JB, Reyes A.
    Scand J Urol Nephrol; 2003 May; 37(1):93-5. PubMed ID: 12745755
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  • 11. A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracranial hypertension.
    Godefroid N, Riveira-Munoz E, Saint-Martin C, Nassogne MC, Dahan K, Devuyst O.
    Am J Kidney Dis; 2006 Nov; 48(5):e73-9. PubMed ID: 17059986
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  • 12. [Familial hypomagnesemia with hypercalciuria and nephrocalcinosis].
    Martín Aguado M, Canals Baeza A, Sanguino López L, Gavilán Martín C, Flores Serrano J.
    An Esp Pediatr; 2001 Feb; 54(2):174-7. PubMed ID: 11181214
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  • 14. Hypomagnesemia-hypercalciuria-nephrocalcinosis and ocular findings: a new claudin-19 mutation.
    Ekinci Z, Karabaş L, Konrad M.
    Turk J Pediatr; 2012 Feb; 54(2):168-70. PubMed ID: 22734304
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  • 17. 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 Feb; 60(1):76-80. PubMed ID: 30102483
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  • 20. Primary familial hypomagnesemia syndrome: a new approach in treatment.
    Nesibe A, Sinasi O.
    J Pediatr Endocrinol Metab; 2012 Feb; 25(5-6):599-602. PubMed ID: 22876566
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