These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

145 related items for PubMed ID: 22574785

  • 1. Glycemic management in living donor liver transplantation for patients with glycogen storage disease type 1b.
    Karaki C, Kasahara M, Sakamoto S, Shigeta T, Uchida H, Kanazawa H, Kakiuchi T, Fukuda A, Nakazawa A, Horikawa R, Suzuki Y.
    Pediatr Transplant; 2012 Aug; 16(5):465-70. PubMed ID: 22574785
    [Abstract] [Full Text] [Related]

  • 2. 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; 15(12):1867-71. PubMed ID: 19938129
    [Abstract] [Full Text] [Related]

  • 3. Longterm Outcomes of Living Donor Liver Transplantation for Glycogen Storage Disease Type 1b.
    Shimizu S, Sakamoto S, Horikawa R, Fukuda A, Uchida H, Takeda M, Yanagi Y, Irie R, Yoshioka T, Kasahara M.
    Liver Transpl; 2020 Jan; 26(1):57-67. PubMed ID: 31587472
    [Abstract] [Full Text] [Related]

  • 4. Immunological features and complications in patients with glycogen storage disease 1b after living donor liver transplantation.
    Shimizu S, Sakamoto S, Yamada M, Fukuda A, Yanagi Y, Uchida H, Mimori K, Shoji K, Funaki T, Miyairi I, Nakano N, Haga C, Yoshioka T, Imadome KI, Horikawa R, Kasahara M.
    Pediatr Transplant; 2021 Dec; 25(8):e14104. PubMed ID: 34339091
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. 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; 40(8):2815-7. PubMed ID: 18929868
    [Abstract] [Full Text] [Related]

  • 7. Historical highlights and unsolved problems in glycogen storage disease type 1.
    Moses SW.
    Eur J Pediatr; 2002 Oct; 161 Suppl 1():S2-9. PubMed ID: 12373565
    [Abstract] [Full Text] [Related]

  • 8. 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; 8(1):106-8. PubMed ID: 19208526
    [Abstract] [Full Text] [Related]

  • 9. Preemptive liver-kidney transplantation in von Gierke disease: a case report.
    Marega A, Fregonese C, Tulissi P, Vallone C, Gropuzzo M, Toniutto PL, Baccarani U, Bresadola F, Toso F, Montanaro D.
    Transplant Proc; 2011 May; 43(4):1196-7. PubMed ID: 21620087
    [Abstract] [Full Text] [Related]

  • 10. Is there any difference in anesthetic management of biliary atresia and glycogen storage disease patients undergoing liver transplantation?
    Jawan B, Tseng CC, Chen YS, Wang CC, Cheng YF, Huang TL, Eng HL, Chiu KW, Wang SH, Lin CC, Lin TS, Liu YW, Chen CL.
    J Surg Res; 2005 Jun 01; 126(1):82-5. PubMed ID: 15916979
    [Abstract] [Full Text] [Related]

  • 11. Perioperative management of benign hepatic tumors in patients with glycogen storage disease type Ia.
    Oshita A, Itamoto T, Amano H, Ohdan H, Tashiro H, Asahara T.
    J Hepatobiliary Pancreat Surg; 2008 Jun 01; 15(2):200-3. PubMed ID: 18392715
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. 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]

  • 14. Living donor liver transplantation in children with cholestatic liver disease: a single-center experience.
    Mizuta K, Urahashi T, Ihara Y, Sanada Y, Wakiya T, Yamada N, Okada N, Egami S, Hishikawa S, Hyodo M, Sakuma Y, Fujiwara T, Kawarasaki H, Yasuda Y.
    Transplant Proc; 2012 Mar 11; 44(2):469-72. PubMed ID: 22410047
    [Abstract] [Full Text] [Related]

  • 15. Living-donor liver transplantation for carbamoyl phosphate synthetase 1 deficiency.
    Kasahara M, Sakamoto S, Shigeta T, Fukuda A, Kosaki R, Nakazawa A, Uemoto S, Noda M, Naiki Y, Horikawa R.
    Pediatr Transplant; 2010 Dec 11; 14(8):1036-40. PubMed ID: 21108709
    [Abstract] [Full Text] [Related]

  • 16. Successful Anesthetic Management of an Adult Patient With Glycogen Storage Disease Type 1 During Liver Transplant: A Case Report.
    Çekmen N, Haka D, Torgay A, Karakaya E, Yıldırım S, Haberal M.
    Exp Clin Transplant; 2024 May 11; 22(5):402-405. PubMed ID: 38970286
    [Abstract] [Full Text] [Related]

  • 17. Living-related donor liver transplantation for children with fulminant hepatic failure in Israel.
    Shouval DS, Mor E, Avitzur Y, Shamir R, Bar-Nathan N, Steinberg R, Schoenfeld T, Ben-Ari Z, Shapiro R.
    J Pediatr Gastroenterol Nutr; 2009 Apr 11; 48(4):451-5. PubMed ID: 19322055
    [Abstract] [Full Text] [Related]

  • 18. Hemodynamic changes during the anhepatic phase in pediatric patient with biliary atresia versus glycogen storage disease undergoing living donor liver transplantation.
    Huang HW, Lu HF, Chiang MH, Chen CL, Wang CH, Cheng KW, Jawan B, Huang CJ, Wu SC.
    Transplant Proc; 2012 Mar 11; 44(2):473-5. PubMed ID: 22410048
    [Abstract] [Full Text] [Related]

  • 19. Diabetes mellitus after living donor liver transplantation: data from mainland China.
    Zhao J, Yan L, Li B, Zeng Y, Wen T, Zhao J, Wang W, Xu M, Yang J, Ma Y, Chen Z, Wu H, Wei Y.
    Transplant Proc; 2009 Jun 11; 41(5):1756-60. PubMed ID: 19545722
    [Abstract] [Full Text] [Related]

  • 20. Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype.
    Weston BW, Lin JL, Muenzer J, Cameron HS, Arnold RR, Seydewitz HH, Mayatepek E, Van Schaftingen E, Veiga-da-Cunha M, Matern D, Chen YT.
    Pediatr Res; 2000 Sep 11; 48(3):329-34. PubMed ID: 10960498
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.