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Journal Abstract Search

132 related items for PubMed ID: 6543856

  • 1. Renal tubular insufficiency, cholestatic jaundice, and multiple congenital anomalies--a new multisystem syndrome.
    Mikati MA, Barakat AY, Sulh HB, Der Kaloustian VM.
    Helv Paediatr Acta; 1984 Dec; 39(5-6):463-71. PubMed ID: 6543856
    [Abstract] [Full Text] [Related]

  • 2. Clinical and pathological aspects of ARC (arthrogryposis, renal dysfunction and cholestasis) syndrome in two siblings.
    Tekin N, Durmuş-Aydoğdu S, Dinleyici EC, Bör O, Bildirici K, Akşit A.
    Turk J Pediatr; 2005 Dec; 47(1):67-70. PubMed ID: 15884633
    [Abstract] [Full Text] [Related]

  • 3. [Arthrogryposis, renal tubular dysfunction, cholestasis (ARC) syndrome: case report and review of the literature].
    Denecke J, Zimmer KP, Kleta R, Koch HG, Rabe H, August C, Harms E.
    Klin Padiatr; 2000 Dec; 212(2):77-80. PubMed ID: 10812557
    [Abstract] [Full Text] [Related]

  • 4. Arthrogryposis, renal dysfunction and cholestasis syndrome.
    Abdullah MA, Al-Hasnan Z, Okamoto E, Abomelha AM.
    Saudi Med J; 2000 Mar; 21(3):297-9. PubMed ID: 11533803
    [Abstract] [Full Text] [Related]

  • 5. A familial syndrome of growth retardation, severe Fanconi-type renal disease and glomerular changes--a new entity?
    Bartsocas CS, Bernstein J, Orloff S, Chandra R, Schulman JD.
    Int J Pediatr Nephrol; 1986 Mar; 7(2):101-6. PubMed ID: 3721723
    [Abstract] [Full Text] [Related]

  • 6. Clinical problems with developmental anomalies of the biliary tract.
    Suchy FJ.
    Semin Gastrointest Dis; 2003 Oct; 14(4):156-64. PubMed ID: 14719766
    [Abstract] [Full Text] [Related]

  • 7. Early detection of severe cholestatic hepatopathy in COACH syndrome.
    Foell D, August C, Frosch M, Harms E, Zimmer KP.
    Am J Med Genet; 2002 Sep 01; 111(4):429-34. PubMed ID: 12210305
    [Abstract] [Full Text] [Related]

  • 8. Novel VIPAS39 mutation in a syndromic patient with arthrogryposis, renal tubular dysfunction and intrahepatic cholestasis.
    Aflatounian M, Smith H, Farahani F, Tofighi Naeem A, Straatman-Iwanowska A, Zoghi S, Khatri U, Tajdini P, Fallahi GH, Gissen P, Rezaei N.
    Eur J Med Genet; 2016 Apr 01; 59(4):237-9. PubMed ID: 26808426
    [Abstract] [Full Text] [Related]

  • 9. Pathology of lethal fetal growth retardation syndrome with aminoaciduria, iron overload, and lactic acidosis (GRACILE).
    Rapola J, Heikkilä P, Fellman V.
    Pediatr Pathol Mol Med; 2002 Apr 01; 21(2):183-93. PubMed ID: 11942535
    [Abstract] [Full Text] [Related]

  • 10. Cerebral defects and nephrogenic diabetes insipidus with the ARC syndrome: additional findings or a new syndrome (ARCC-NDI)?
    Coleman RA, Van Hove JL, Morris CR, Rhoads JM, Summar ML.
    Am J Med Genet; 1997 Oct 31; 72(3):335-8. PubMed ID: 9332665
    [Abstract] [Full Text] [Related]

  • 11. [Cortical renal microcysts in Lowe's syndrome].
    López Garrido J, Armas Padrón JR, González-Cámpora R, Galera Davidson H, Camacho González F, Estefanía Gallardo C.
    An Esp Pediatr; 1985 Jun 31; 22(8):571-4. PubMed ID: 4051342
    [Abstract] [Full Text] [Related]

  • 12. New syndrome or severe expression of Gordon syndrome? A case report.
    Courtens W, Perlmutter N, Dan B, Vamos E.
    Clin Dysmorphol; 1997 Jan 31; 6(1):39-44. PubMed ID: 9018417
    [Abstract] [Full Text] [Related]

  • 13. Pseudohypoaldosteronism.
    Blachar Y, Kaplan BS, Griffel B, Levin S.
    Clin Nephrol; 1979 Jun 31; 11(6):281-8. PubMed ID: 477044
    [Abstract] [Full Text] [Related]

  • 14.
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  • 15. Association of bilateral renal dysplasia and congenital hepatic fibrosis.
    Proesmans W, Moerman P, Depraetere M, Van Damme B.
    Int J Pediatr Nephrol; 1986 Jun 31; 7(2):113-6. PubMed ID: 3721724
    [Abstract] [Full Text] [Related]

  • 16. Partially reversible renal tubular damage in patients with obstructive jaundice.
    Bairaktari E, Liamis G, Tsolas O, Elisaf M.
    Hepatology; 2001 Jun 31; 33(6):1365-9. PubMed ID: 11391524
    [Abstract] [Full Text] [Related]

  • 17. Arc syndrome without arthrogryposis, with hip dislocation and renal glomerulocystic appearance: a case report.
    Arhan E, Yusufoğlu AM, Sayli TR.
    Eur J Pediatr; 2009 Aug 31; 168(8):995-8. PubMed ID: 18972129
    [Abstract] [Full Text] [Related]

  • 18.
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  • 19. Severe congenital anomalies requiring transplantation in children with Kabuki syndrome.
    Ewart-Toland A, Enns GM, Cox VA, Mohan GC, Rosenthal P, Golabi M.
    Am J Med Genet; 1998 Dec 04; 80(4):362-7. PubMed ID: 9856564
    [Abstract] [Full Text] [Related]

  • 20. Liver biopsy complicated by hemorrhage in a patient with ARC syndrome.
    Hayes JA, Kahr WH, Lo B, Macpherson BA.
    Paediatr Anaesth; 2004 Nov 04; 14(11):960-3. PubMed ID: 15500499
    [Abstract] [Full Text] [Related]

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