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Journal Abstract Search

136 related items for PubMed ID: 7742209

  • 41. Nephrocalcinosis and nephrolithiasis due to subcutaneous fat necrosis with hypercalcemia in two full-term asphyxiated neonates: sonographic findings.
    Gu LL, Daneman A, Binet A, Kooh SW.
    Pediatr Radiol; 1995; 25(2):142-4. PubMed ID: 7596662
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  • 42. Nephrocalcinosis in Bartter's syndrome.
    Garel L, Filiatrault D, Robitaille P.
    Pediatr Nephrol; 1988 Jul; 2(3):315-7. PubMed ID: 3153033
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  • 43. Neonatal nephrocalcinosis in association with glucose-galactose malabsorption.
    Pahari A, Milla PJ, van't Hoff WG.
    Pediatr Nephrol; 2003 Jul; 18(7):700-2. PubMed ID: 12734749
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  • 44. A case of Menkes' disease with nephrocalcinosis and chronic renal failure.
    Balestracci A, Caletti MG, Missoni M.
    Pediatr Nephrol; 2009 Jun; 24(6):1255-6. PubMed ID: 19139924
    [No Abstract] [Full Text] [Related]

  • 45. Clinical aspects of calcium metabolism.
    Harrison AR.
    Trans Med Soc Lond; 1970 Jun; 86():55-62. PubMed ID: 5494698
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  • 50. Renal medullary "rings": possible CT manifestation of hypercalcemia.
    Curry NS, Gordon L, Gobien RP, Lott M.
    Urol Radiol; 1984 Jun; 6(1):48-50. PubMed ID: 6702030
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  • 51. Hypercalciuria and nephrocalcinosis in the oculocerebrorenal syndrome.
    Sliman GA, Winters WD, Shaw DW, Avner ED.
    J Urol; 1995 Apr; 153(4):1244-6. PubMed ID: 7869519
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  • 53. Discordant Clinical Course of Vitamin-D-Hydroxylase (CYP24A1) Associated Hypercalcemia in Two Adult Brothers With Nephrocalcinosis.
    Jobst-Schwan T, Pannes A, Schlingmann KP, Eckardt KU, Beck BB, Wiesener MS.
    Kidney Blood Press Res; 2015 Apr; 40(5):443-51. PubMed ID: 26304832
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  • 54. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: blocking endocytosis restores surface expression of a novel Claudin-16 mutant that lacks the entire C-terminal cytosolic tail.
    Müller D, Kausalya PJ, Meij IC, Hunziker W.
    Hum Mol Genet; 2006 Apr 01; 15(7):1049-58. PubMed ID: 16501001
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  • 55. Increased renal medullary echogenicity in patients with Williams syndrome.
    Cote G, Jequier S, Kaplan P.
    Pediatr Radiol; 1989 Apr 01; 19(6-7):481-3. PubMed ID: 2671904
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  • 56. Enamel renal syndrome: a rare case report.
    Kala Vani SV, Varsha M, Sankar YU.
    J Indian Soc Pedod Prev Dent; 2012 Apr 01; 30(2):169-72. PubMed ID: 22918105
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  • 60. Hyperechoic renal medullary pyramids in infants and children.
    Shultz PK, Strife JL, Strife CF, McDaniel JD.
    Radiology; 1991 Oct 01; 181(1):163-7. PubMed ID: 1887027
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