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248 related items for PubMed ID: 35313948

  • 1. 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]

  • 2. 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]

  • 3. Diagnosis of hepatic glycogen storage disease patients with overlapping clinical symptoms by massively parallel sequencing: a systematic review of literature.
    Beyzaei Z, Geramizadeh B, Karimzadeh S.
    Orphanet J Rare Dis; 2020 Oct 14; 15(1):286. PubMed ID: 33054851
    [Abstract] [Full Text] [Related]

  • 4. Glycogen storage diseases with liver involvement: a literature review of GSD type 0, IV, VI, IX and XI.
    Massese M, Tagliaferri F, Dionisi-Vici C, Maiorana A.
    Orphanet J Rare Dis; 2022 Jun 20; 17(1):241. PubMed ID: 35725468
    [Abstract] [Full Text] [Related]

  • 5. 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 20; 158 Suppl 2(Suppl 2):S43-8. PubMed ID: 10603098
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
    Kishnani PS, Goldstein J, Austin SL, Arn P, Bachrach B, Bali DS, Chung WK, El-Gharbawy A, Brown LM, Kahler S, Pendyal S, Ross KM, Tsilianidis L, Weinstein DA, Watson MS, ACMG Work Group on Diagnosis and Management of Glycogen Storage Diseases Type VI and IX.
    Genet Med; 2019 Apr 11; 21(4):772-789. PubMed ID: 30659246
    [Abstract] [Full Text] [Related]

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

  • 9. Long-term outcome after liver transplantation in children with type 1 glycogen storage disease.
    Yuen WY, Quak SH, Aw MM, Karthik SV.
    Pediatr Transplant; 2021 Mar 11; 25(2):e13872. PubMed ID: 33044776
    [Abstract] [Full Text] [Related]

  • 10. 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 11; 51(3):483-90. PubMed ID: 19596478
    [Abstract] [Full Text] [Related]

  • 11. The natural history of glycogen storage disease types VI and IX: Long-term outcome from the largest metabolic center in Canada.
    Roscher A, Patel J, Hewson S, Nagy L, Feigenbaum A, Kronick J, Raiman J, Schulze A, Siriwardena K, Mercimek-Mahmutoglu S.
    Mol Genet Metab; 2014 Nov 11; 113(3):171-6. PubMed ID: 25266922
    [Abstract] [Full Text] [Related]

  • 12. 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 11; 13(6):848-52. PubMed ID: 17539004
    [Abstract] [Full Text] [Related]

  • 13. Genotypic and phenotypic features of 39 Chinese patients with glycogen storage diseases type I, VI, and IX.
    Yu J, Ling X, Chen L, Fang Y, Lin H, Lou J, Ren Y, Chen J.
    Clin Genet; 2024 Sep 11; 106(3):267-276. PubMed ID: 38576397
    [Abstract] [Full Text] [Related]

  • 14. Elevated serum biotinidase activity in hepatic glycogen storage disorders--a convenient biomarker.
    Paesold-Burda P, Baumgartner MR, Santer R, Bosshard NU, Steinmann B.
    J Inherit Metab Dis; 2007 Nov 11; 30(6):896-902. PubMed ID: 17994282
    [Abstract] [Full Text] [Related]

  • 15. Gene therapy for glycogen storage diseases.
    Koeberl DD, Koch RL, Lim JA, Brooks ED, Arnson BD, Sun B, Kishnani PS.
    J Inherit Metab Dis; 2024 Jan 11; 47(1):93-118. PubMed ID: 37421310
    [Abstract] [Full Text] [Related]

  • 16. Nutrition therapy for hepatic glycogen storage diseases.
    Goldberg T, Slonim AE.
    J Am Diet Assoc; 1993 Dec 11; 93(12):1423-30. PubMed ID: 8245377
    [Abstract] [Full Text] [Related]

  • 17. [Clinico-biochemical and morphological characteristics of the hepatic form of glycogenosis in children].
    Popovich IuG, Chibisov IV, Potapova-Vinogradova IN, Chistova LV.
    Pediatriia; 1988 Dec 11; (1):35-9. PubMed ID: 3163143
    [No Abstract] [Full Text] [Related]

  • 18. Glycogen storage diseases: An update.
    Gümüş E, Özen H.
    World J Gastroenterol; 2023 Jul 07; 29(25):3932-3963. PubMed ID: 37476587
    [Abstract] [Full Text] [Related]

  • 19. [Mitochondrial dysfunction in children with hepatic forms of glycogen storage disease].
    Kurbatova OV, Izmaĭlova TD, Surkov AN, Namazova-Baranova LS, Poliakova SI, Miroshkina LV, Semenova GF, Samokhina IV, Kapustina EIu, Dukhova ZN, Potapov AS, Petrichuk SV.
    Vestn Ross Akad Med Nauk; 2014 Jul 07; (7-8):78-84. PubMed ID: 25563007
    [Abstract] [Full Text] [Related]

  • 20. Biomarkers in Glycogen Storage Diseases: An Update.
    Molares-Vila A, Corbalán-Rivas A, Carnero-Gregorio M, González-Cespón JL, Rodríguez-Cerdeira C.
    Int J Mol Sci; 2021 Apr 22; 22(9):. PubMed ID: 33922238
    [Abstract] [Full Text] [Related]

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