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Journal Abstract Search

142 related items for PubMed ID: 16433006

  • 21. Glycogen storage disease type I: indications for liver and/or kidney transplantation.
    Labrune P.
    Eur J Pediatr; 2002 Oct; 161 Suppl 1():S53-5. PubMed ID: 12373572
    [Abstract] [Full Text] [Related]

  • 22. Combined liver-kidney transplantation in glycogen storage disease Ia: a case beyond the guidelines.
    Belingheri M, Ghio L, Sala A, Menni F, Trespidi L, Ferraresso M, Berardinelli L, Rossi G, Edefonti A, Parini R.
    Liver Transpl; 2007 May; 13(5):762-4. PubMed ID: 17457869
    [Abstract] [Full Text] [Related]

  • 23. Hepatic lentiviral gene transfer prevents the long-term onset of hepatic tumours of glycogen storage disease type 1a in mice.
    Clar J, Mutel E, Gri B, Creneguy A, Stefanutti A, Gaillard S, Ferry N, Beuf O, Mithieux G, Nguyen TH, Rajas F.
    Hum Mol Genet; 2015 Apr 15; 24(8):2287-96. PubMed ID: 25561689
    [Abstract] [Full Text] [Related]

  • 24. Cyclosporine A withdrawal during follow-up after pediatric liver transplantation.
    Scheenstra R, Torringa ML, Waalkens HJ, Middelveld EH, Peeters PM, Slooff MJ, Gouw AS, Verkade HJ, Bijleveld CM.
    Liver Transpl; 2006 Feb 15; 12(2):240-6. PubMed ID: 16447209
    [Abstract] [Full Text] [Related]

  • 25. Prevention of complications in glycogen storage disease type Ia with optimization of metabolic control.
    Dambska M, Labrador EB, Kuo CL, Weinstein DA.
    Pediatr Diabetes; 2017 Aug 15; 18(5):327-331. PubMed ID: 28568353
    [Abstract] [Full Text] [Related]

  • 26. Fifteen years of follow-up of a liver transplant recipient with glycogen storage disease type Ia (Von Gierke disease).
    Maya Aparicio AC, Bernal Bellido C, Tinoco González J, Garcia Ruíz S, Aguilar Romero L, Marín Gómez LM, Suárez Artacho G, Alamo Martínez JM, Serrano Díez-Canedo J, Padillo Ruíz FJ, Gomez Bravo MA.
    Transplant Proc; 2013 Aug 15; 45(10):3668-9. PubMed ID: 24314991
    [Abstract] [Full Text] [Related]

  • 27. An infant presenting with extreme hypertriglyceridemia diagnosed as glycogen storage disease type Ia.
    Fang LJ, Abuduxikuer K, Yan XM, Zhu H, Huang KY.
    J Pediatr Endocrinol Metab; 2020 May 21; 33(6):803-808. PubMed ID: 32436859
    [Abstract] [Full Text] [Related]

  • 28. A 20-year follow-up of a male patient with type Ia glycogen storage disease.
    Hou JW, Wang TR.
    Chang Gung Med J; 2003 Apr 21; 26(4):283-7. PubMed ID: 12846528
    [Abstract] [Full Text] [Related]

  • 29. Regression of hepatic adenomas in type Ia glycogen storage disease with dietary therapy.
    Parker P, Burr I, Slonim A, Ghishan FK, Greene H.
    Gastroenterology; 1981 Sep 21; 81(3):534-6. PubMed ID: 6941908
    [Abstract] [Full Text] [Related]

  • 30. Hepatocyte transplantation using the domino concept in a child with tetrabiopterin nonresponsive phenylketonuria.
    Stéphenne X, Debray FG, Smets F, Jazouli N, Sana G, Tondreau T, Menten R, Goffette P, Boemer F, Schoos R, Gersting SW, Najimi M, Muntau AC, Goyens P, Sokal EM.
    Cell Transplant; 2012 Sep 21; 21(12):2765-70. PubMed ID: 22889463
    [Abstract] [Full Text] [Related]

  • 31. Early, sustained efficacy of adeno-associated virus vector-mediated gene therapy in glycogen storage disease type Ia.
    Koeberl DD, Sun BD, Damodaran TV, Brown T, Millington DS, Benjamin DK, Bird A, Schneider A, Hillman S, Jackson M, Beaty RM, Chen YT.
    Gene Ther; 2006 Sep 21; 13(17):1281-9. PubMed ID: 16672983
    [Abstract] [Full Text] [Related]

  • 32. One liver for four children: first clinical series of liver cell transplantation for severe neonatal urea cycle defects.
    Meyburg J, Das AM, Hoerster F, Lindner M, Kriegbaum H, Engelmann G, Schmidt J, Ott M, Pettenazzo A, Luecke T, Bertram H, Hoffmann GF, Burlina A.
    Transplantation; 2009 Mar 15; 87(5):636-41. PubMed ID: 19295306
    [Abstract] [Full Text] [Related]

  • 33. Long-term correction of murine glycogen storage disease type Ia by recombinant adeno-associated virus-1-mediated gene transfer.
    Ghosh A, Allamarvdasht M, Pan CJ, Sun MS, Mansfield BC, Byrne BJ, Chou JY.
    Gene Ther; 2006 Feb 15; 13(4):321-9. PubMed ID: 16195703
    [Abstract] [Full Text] [Related]

  • 34. Glycogen storage disease type Ia and VI associated with hepatocellular carcinoma: two case reports.
    Manzia TM, Angelico R, Toti L, Cillis A, Ciano P, Orlando G, Anselmo A, Angelico M, Tisone G.
    Transplant Proc; 2011 May 15; 43(4):1181-3. PubMed ID: 21620082
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36. Glycogen storage disease type I--between chronic ambulatory follow-up and pediatric emergency.
    Moraru E, Cuvinciuc O, Antonesei L, Mihaila D, Bozomitu L, Rusu T, Stana B, Sacaci P, Luchian A, Bratu L, Popescu A, Mircan O, Moraru D.
    J Gastrointestin Liver Dis; 2007 Mar 15; 16(1):47-51. PubMed ID: 17410288
    [Abstract] [Full Text] [Related]

  • 37.
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  • 38. Safety assessment of intraportal liver cell application in New Zealand white rabbits under GLP conditions.
    Kafert-Kasting S, Schneider A, Attaran M, Priesner C, Barthold M, Perrier AL, Kriegbaum H, Ott M, Meyburg J.
    Arch Toxicol; 2012 Sep 15; 86(9):1413-22. PubMed ID: 22532025
    [Abstract] [Full Text] [Related]

  • 39. Reduced-size liver transplantation for glycogen storage disease.
    Ji HF, Wang WL, Shen Y, Zhang M, Liang TB, Wu J, Xu X, Yan S, Zheng SS.
    Hepatobiliary Pancreat Dis Int; 2009 Feb 15; 8(1):106-8. PubMed ID: 19208526
    [Abstract] [Full Text] [Related]

  • 40. Long-term results of living donor liver transplantation for glycogen storage disorders in children.
    Iyer SG, Chen CL, Wang CC, Wang SH, Concejero AM, Liu YW, Yang CH, Yong CC, Jawan B, Cheng YF, Eng HL.
    Liver Transpl; 2007 Jun 15; 13(6):848-52. PubMed ID: 17539004
    [Abstract] [Full Text] [Related]

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