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Journal Abstract Search

239 related items for PubMed ID: 25165176

  • 41. Two cases of Fanconi-Bickel syndrome: first report from China with novel mutations of SLC2A2 gene.
    Su Z, Du ML, Chen HS, Chen QL, Yu CS, Mal HM.
    J Pediatr Endocrinol Metab; 2011; 24(9-10):749-53. PubMed ID: 22145468
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  • 44. Importance about use of high-throughput sequencing in pediatric: case report of a patient with Fanconi-Bickel syndrome.
    Abarca-Barriga HH, Laso-Salazar MC, Orihuela-Tacuri D, Chirinos-Saire J, Venero-Nuñez A.
    BMC Pediatr; 2024 Mar 07; 24(1):161. PubMed ID: 38454379
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  • 46. Fanconi-Bickel syndrome.
    Mohandas Nair K, Sakamoto O, Jagadeesh S, Nampoothiri S.
    Indian J Pediatr; 2012 Jan 07; 79(1):112-4. PubMed ID: 21327337
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  • 48. No mutation in the SLC2A2 ( GLUT2) gene in a Turkish infant with Fanconi-Bickel syndrome.
    Ozer EA, Aksu N, Uclar E, Erdogan H, Bakiler AR, Tsuda M, Kitasawa E, Coker M, Ozer E.
    Pediatr Nephrol; 2003 Apr 07; 18(4):397-8. PubMed ID: 12700970
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  • 50. Fanconi-Bickel syndrome--a congenital defect of facilitative glucose transport.
    Santer R, Steinmann B, Schaub J.
    Curr Mol Med; 2002 Mar 07; 2(2):213-27. PubMed ID: 11949937
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  • 54. Fanconi-Bickel syndrome as an example of marked allelic heterogeneity.
    Al-Haggar M.
    World J Nephrol; 2012 Jun 06; 1(3):63-8. PubMed ID: 24175243
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  • 56. [The Fanconi-Bickel syndrome].
    Velásquez L, Portillo VH, Sanjinés R, Gamboa JD, Feria-Kaiser C, Valencia P.
    Bol Med Hosp Infant Mex; 1991 Apr 06; 48(4):255-60. PubMed ID: 1867746
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  • 59. A novel mutation in the GLUT2 gene in a patient with Fanconi-Bickel syndrome detected by neonatal screening for galactosaemia.
    Peduto A, Spada M, Alluto A, La Dolcetta M, Ponzone A, Santer R.
    J Inherit Metab Dis; 2004 Apr 06; 27(2):279-80. PubMed ID: 15243984
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  • 60. Novel Fanconi renotubular syndromes provide insights in proximal tubule pathophysiology.
    Lemaire M.
    Am J Physiol Renal Physiol; 2021 Feb 01; 320(2):F145-F160. PubMed ID: 33283647
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