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Journal Abstract Search


243 related items for PubMed ID: 30454741

  • 1. Fanconi Syndrome.
    Foreman JW.
    Pediatr Clin North Am; 2019 Feb; 66(1):159-167. PubMed ID: 30454741
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  • 4. A case of severe osteomalacia caused by Tubulointerstitial nephritis with Fanconi syndrome in asymptomotic primary biliary cirrhosis.
    Yamaguchi S, Maruyama T, Wakino S, Tokuyama H, Hashiguchi A, Tada S, Homma K, Monkawa T, Thomas J, Miyashita K, Kurihara I, Yoshida T, Konishi K, Hayashi K, Hayashi M, Itoh H.
    BMC Nephrol; 2015 Nov 11; 16():187. PubMed ID: 26554665
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  • 5. [Primary Toni-Debré-Fanconi syndrome].
    Berio A.
    Pediatr Med Chir; 1993 Nov 11; 15(1):79-85. PubMed ID: 8488131
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  • 6. Severe renal tubulopathy in a newborn due to BCS1L gene mutation: effects of different treatment modalities on the clinical course.
    Ezgu F, Senaca S, Gunduz M, Tumer L, Hasanoglu A, Tiras U, Unsal R, Bakkaloglu SA.
    Gene; 2013 Oct 10; 528(2):364-6. PubMed ID: 23892085
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  • 7. Transient renal Fanconi syndrome in a Chihuahua exposed to Chinese chicken jerky treats.
    Hooijberg EH, Furman E, Leidinger J, Brandstetter D, Hochleithner C, Sewell AC, Leidinger E, Giger U.
    Tierarztl Prax Ausg K Kleintiere Heimtiere; 2015 Oct 10; 43(3):188-92. PubMed ID: 25966748
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  • 9. Fanconi Syndrome in Irish Wolfhound Siblings.
    Bommer NX, Brownlie SE, Morrison LR, Chandler ML, Simpson JW.
    J Am Anim Hosp Assoc; 2018 Oct 10; 54(3):173-178. PubMed ID: 29558216
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  • 10. The renal Fanconi syndrome in cystinosis: pathogenic insights and therapeutic perspectives.
    Cherqui S, Courtoy PJ.
    Nat Rev Nephrol; 2017 Feb 10; 13(2):115-131. PubMed ID: 27990015
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  • 11. [Renal glucosuria].
    Rohfleisch A, Nseir G, Chehade H, Noverraz MG, Venetz JP, Barbey F.
    Rev Med Suisse; 2013 Mar 20; 9(378):636-40. PubMed ID: 23547366
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  • 12. The Case. A child with metabolic acidosis and growth retardation.
    Sahay M, Vali SP, Ramesh VD.
    Kidney Int; 2009 May 20; 75(10):1121-2. PubMed ID: 19404298
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  • 13. Idiopathic Fanconi syndrome with progressive renal failure: a case report and discussion.
    Long WS, Seashore MR, Siegel NJ, Bia MJ.
    Yale J Biol Med; 1990 May 20; 63(1):15-28. PubMed ID: 2356624
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  • 15. Clinical manifestation and genetic findings in three boys with low molecular Weight Proteinuria - three case reports for exploring Dent Disease and Fanconi syndrome.
    Duan N, Huang C, Pang L, Jiang S, Yang W, Li H.
    BMC Nephrol; 2021 Jan 11; 22(1):24. PubMed ID: 33430795
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  • 16. Cystinosis presenting with findings of Bartter syndrome.
    Özkan B, Çayır A, Koşan C, Alp H.
    J Clin Res Pediatr Endocrinol; 2011 Jan 11; 3(2):101-4. PubMed ID: 21750641
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  • 19. Nephropathic infantile form of cystinosis about one case.
    Sfaihi L, Aloulou H, Ben Amor S, Kamoun T, Hachicha M.
    Fetal Pediatr Pathol; 2013 Feb 11; 31(1):66-70. PubMed ID: 22497686
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