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188 related items for PubMed ID: 34635148
1. 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]
2. 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]
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 11; 13(6):848-52. PubMed ID: 17539004 [Abstract] [Full Text] [Related]
4. 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]
5. Impact of hematopoietic stem cell transplantation in glycogen storage disease type Ib: A single-subject research design using 13C-glucose breath test. Turki A, Stockler S, Sirrs S, Duddy K, Ho G, Elango R. Mol Genet Metab Rep; 2023 Mar 21; 34():100955. PubMed ID: 36632325 [Abstract] [Full Text] [Related]
6. Outcomes of liver transplantation for glycogen storage disease: a matched-control study and a review of literature. Maheshwari A, Rankin R, Segev DL, Thuluvath PJ. Clin Transplant; 2012 Mar 21; 26(3):432-6. PubMed ID: 22066793 [Abstract] [Full Text] [Related]
7. Outcome of liver transplantation in hepatic glycogen storage disease: A systematic review and meta-analysis. Beyzaei Z, Bagheri Z, Karimzadeh S, Geramizadeh B. Clin Transplant; 2023 Mar 21; 37(3):e14867. PubMed ID: 36433721 [Abstract] [Full Text] [Related]
8. Clinical spectrum, over 12-year follow-up and experience of SGLT2 inhibitors treatment on patients with glycogen storage disease type Ib: a single-center retrospective study. Shao YX, Liang CL, Su YY, Lin YT, Lu ZK, Lin RZ, Zhou ZZ, Zeng CH, Tao CY, Liu ZC, Zhang W, Liu L. Orphanet J Rare Dis; 2024 Apr 11; 19(1):155. PubMed ID: 38605407 [Abstract] [Full Text] [Related]
9. Favorable Kidney Function in Pediatric Liver Transplant Recipients: Results of a Single-center Cohort Study. Sato M, Kaneko T, Ogura M, Kamei K, Ito S, Fukuda A, Sakamoto S, Kasahara M, Ishikura K. Transplantation; 2019 Aug 11; 103(8):1655-1662. PubMed ID: 30489480 [Abstract] [Full Text] [Related]
10. Living donor liver transplantation for glycogen storage disease type Ib. Kasahara M, Horikawa R, Sakamoto S, Shigeta T, Tanaka H, Fukuda A, Abe K, Yoshii K, Naiki Y, Kosaki R, Nakagawa A. Liver Transpl; 2009 Dec 11; 15(12):1867-71. PubMed ID: 19938129 [Abstract] [Full Text] [Related]
11. 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]
12. 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]
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. Renal function in glycogen storage disease type I, natural course, and renopreservative effects of ACE inhibition. Martens DH, Rake JP, Navis G, Fidler V, van Dael CM, Smit GP. Clin J Am Soc Nephrol; 2009 Nov 06; 4(11):1741-6. PubMed ID: 19808227 [Abstract] [Full Text] [Related]
15. Preemptive living donor liver transplantation in glycogen storage disease Ia: case report. Kaihara S, Ushigome H, Sakai K, Yoshizawa A, Nobori S, Suzuki T, Okamoto M, Ochiai T, Yoshimura N. Transplant Proc; 2008 Oct 06; 40(8):2815-7. PubMed ID: 18929868 [Abstract] [Full Text] [Related]
16. Continuous glucose monitoring in children with glycogen storage disease type I. Kasapkara ÇS, Cinasal Demir G, Hasanoğlu A, Tümer L. Eur J Clin Nutr; 2014 Jan 06; 68(1):101-5. PubMed ID: 24149443 [Abstract] [Full Text] [Related]
17. Impact of glycogen storage disease type I on adult daily life: a survey. Garbade SF, Ederer V, Burgard P, Wendel U, Spiekerkoetter U, Haas D, Grünert SC. Orphanet J Rare Dis; 2021 Sep 03; 16(1):371. PubMed ID: 34479584 [Abstract] [Full Text] [Related]
18. 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 03; 158 Suppl 2(Suppl 2):S43-8. PubMed ID: 10603098 [Abstract] [Full Text] [Related]
19. [Heterogeneous phenotypes in Chinese glycogen storage disease type Ia patients with homozygous G727T mutation]. Qiu ZQ, Wei M, Liu G, Liu GY. Zhonghua Er Ke Za Zhi; 2003 Apr 03; 41(4):252-5. PubMed ID: 14754525 [Abstract] [Full Text] [Related]
20. The prevalence of polycystic ovaries in the hepatic glycogen storage diseases: its association with hyperinsulinism. Lee PJ, Patel A, Hindmarsh PC, Mowat AP, Leonard JV. Clin Endocrinol (Oxf); 1995 Jun 03; 42(6):601-6. PubMed ID: 7634500 [Abstract] [Full Text] [Related] Page: [Next] [New Search]