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364 related items for PubMed ID: 10603098

  • 1. Liver transplantation for glycogen storage disease types I, III, and IV.
    Matern D, Starzl TE, Arnaout W, Barnard J, Bynon JS, Dhawan A, Emond J, Haagsma EB, Hug G, Lachaux A, Smit GP, Chen YT.
    Eur J Pediatr; 1999 Dec; 158 Suppl 2(Suppl 2):S43-8. PubMed ID: 10603098
    [Abstract] [Full Text] [Related]

  • 2. Liver transplantation for type I and type IV glycogen storage disease.
    Selby R, Starzl TE, Yunis E, Todo S, Tzakis AG, Brown BI, Kendall RS.
    Eur J Pediatr; 1993 Dec; 152 Suppl 1(Suppl 1):S71-6. PubMed ID: 8319729
    [Abstract] [Full Text] [Related]

  • 3. 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; 13(6):848-52. PubMed ID: 17539004
    [Abstract] [Full Text] [Related]

  • 4. Nutrition therapy for hepatic glycogen storage diseases.
    Goldberg T, Slonim AE.
    J Am Diet Assoc; 1993 Dec; 93(12):1423-30. PubMed ID: 8245377
    [Abstract] [Full Text] [Related]

  • 5. Hepatocellular Adenomas and Carcinoma in Asymptomatic, Non-Cirrhotic Type III Glycogen Storage Disease.
    Oterdoom LH, Verweij KE, Biermann K, Langeveld M, van Buuren HR.
    J Gastrointestin Liver Dis; 2015 Dec; 24(4):515-8. PubMed ID: 26697579
    [Abstract] [Full Text] [Related]

  • 6. Liver transplantation in glycogen storage disease: a single-center experience.
    Beyzaei Z, Shamsaeefar A, Kazemi K, Nikeghbalian S, Bahador A, Dehghani M, Malekhosseini SA, Geramizadeh B.
    Orphanet J Rare Dis; 2022 Mar 21; 17(1):127. PubMed ID: 35313948
    [Abstract] [Full Text] [Related]

  • 7. Hepatic glycogen storage disorders: what have we learned in recent years?
    Burda P, Hochuli M.
    Curr Opin Clin Nutr Metab Care; 2015 Jul 21; 18(4):415-21. PubMed ID: 26001652
    [Abstract] [Full Text] [Related]

  • 8. 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 21; 43(4):1181-3. PubMed ID: 21620082
    [Abstract] [Full Text] [Related]

  • 9. Long-term outcome of liver transplantation in patients with glycogen storage disease type Ia.
    Faivre L, Houssin D, Valayer J, Brouard J, Hadchouel M, Bernard O.
    J Inherit Metab Dis; 1999 Aug 21; 22(6):723-32. PubMed ID: 10472532
    [Abstract] [Full Text] [Related]

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

  • 11. Hepatic ultrasound findings in the glycogen storage diseases.
    Lee P, Mather S, Owens C, Leonard J, Dicks-Mireaux C.
    Br J Radiol; 1994 Nov 21; 67(803):1062-6. PubMed ID: 7820397
    [Abstract] [Full Text] [Related]

  • 12. Clinical and laboratory findings in four patients with the non-progressive hepatic form of type IV glycogen storage disease.
    McConkie-Rosell A, Wilson C, Piccoli DA, Boyle J, DeClue T, Kishnani P, Shen JJ, Boney A, Brown B, Chen YT.
    J Inherit Metab Dis; 1996 Nov 21; 19(1):51-8. PubMed ID: 8830177
    [Abstract] [Full Text] [Related]

  • 13. A case study of a liver transplant-treated patient with glycogen storage disease type Ia presenting with multiple inflammatory hepatic adenomas: an analysis of clinicopathologic and genetic data.
    Wang A, Wu J, Yuan X, Liu J, Lu C.
    BMC Med Genomics; 2024 May 06; 17(1):124. PubMed ID: 38711024
    [Abstract] [Full Text] [Related]

  • 14. Modifiable factors affecting renal preservation in type I glycogen storage disease after liver transplantation: a single-center propensity-match cohort study.
    Chan YC, Liu KM, Chen CL, Ong AD, Lin CC, Yong CC, Tsai PC, Lu LS, Wu JY.
    Orphanet J Rare Dis; 2021 Oct 11; 16(1):423. PubMed ID: 34635148
    [Abstract] [Full Text] [Related]

  • 15. Natural history study of hepatic glycogen storage disease type IV and comparison to Gbe1ys/ys model.
    Koch RL, Kiely BT, Choi SJ, Jeck WR, Flores LS, Sood V, Alam S, Porta G, LaVecchio K, Soler-Alfonso C, Kishnani PS.
    JCI Insight; 2024 May 14; 9(12):. PubMed ID: 38912588
    [Abstract] [Full Text] [Related]

  • 16. Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene.
    Bao Y, Kishnani P, Wu JY, Chen YT.
    J Clin Invest; 1996 Feb 15; 97(4):941-8. PubMed ID: 8613547
    [Abstract] [Full Text] [Related]

  • 17. Long-term follow-up of portacaval shunt in glycogen storage disease type 1B.
    Corbeel L, Van Lierde S, Jaeken J.
    Eur J Pediatr; 2000 Apr 15; 159(4):268-72. PubMed ID: 10789932
    [Abstract] [Full Text] [Related]

  • 18. Liver transplantation for glycogen storage disease type Ia.
    Reddy SK, Austin SL, Spencer-Manzon M, Koeberl DD, Clary BM, Desai DM, Smith AD, Kishnani PS.
    J Hepatol; 2009 Sep 15; 51(3):483-90. PubMed ID: 19596478
    [Abstract] [Full Text] [Related]

  • 19. Liver fibrosis during clinical ascertainment of glycogen storage disease type III: a need for improved and systematic monitoring.
    Halaby CA, Young SP, Austin S, Stefanescu E, Bali D, Clinton LK, Smith B, Pendyal S, Upadia J, Schooler GR, Mavis AM, Kishnani PS.
    Genet Med; 2019 Dec 15; 21(12):2686-2694. PubMed ID: 31263214
    [Abstract] [Full Text] [Related]

  • 20. Reappraisal of the Role of Portacaval Shunting in the Growth of Patients With Glycogen Storage Disease Type I in the Era of Liver Transplantation.
    Choi Y, Yi NJ, Ko JS, Moon JS, Suh SW, Lee JM, Jeong JH, Kim H, Lee HW, Lee KW, Suh KS.
    Transplantation; 2016 Mar 15; 100(3):585-92. PubMed ID: 26360666
    [Abstract] [Full Text] [Related]

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