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Journal Abstract Search

158 related items for PubMed ID: 21108709

  • 1.
    ; . PubMed ID:
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  • 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. Developmental outcomes with early orthotopic liver transplantation for infants with neonatal-onset urea cycle defects and a female patient with late-onset ornithine transcarbamylase deficiency.
    McBride KL, Miller G, Carter S, Karpen S, Goss J, Lee B.
    Pediatrics; 2004 Oct; 114(4):e523-6. PubMed ID: 15466081
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  • 4. Living-donor liver transplantation for propionic acidemia.
    Kasahara M, Sakamoto S, Kanazawa H, Karaki C, Kakiuchi T, Shigeta T, Fukuda A, Kosaki R, Nakazawa A, Ishige M, Nagao M, Shigematsu Y, Yorifuji T, Naiki Y, Horikawa R.
    Pediatr Transplant; 2012 May; 16(3):230-4. PubMed ID: 22151065
    [Abstract] [Full Text] [Related]

  • 5. Current role of liver transplantation for the treatment of urea cycle disorders: a review of the worldwide English literature and 13 cases at Kyoto University.
    Morioka D, Kasahara M, Takada Y, Shirouzu Y, Taira K, Sakamoto S, Uryuhara K, Egawa H, Shimada H, Tanaka K.
    Liver Transpl; 2005 Nov; 11(11):1332-42. PubMed ID: 16237708
    [Abstract] [Full Text] [Related]

  • 6. Living donor liver transplantation for ornithine transcarbamylase deficiency.
    Wakiya T, Sanada Y, Mizuta K, Umehara M, Urahasi T, Egami S, Hishikawa S, Fujiwara T, Sakuma Y, Hyodo M, Murayama K, Hakamada K, Yasuda Y, Kawarasaki H.
    Pediatr Transplant; 2011 Jun; 15(4):390-5. PubMed ID: 21585627
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  • 8. Graft and patient survival after adult live donor liver transplantation compared to a matched cohort who received a deceased donor transplantation.
    Thuluvath PJ, Yoo HY.
    Liver Transpl; 2004 Oct; 10(10):1263-8. PubMed ID: 15376301
    [Abstract] [Full Text] [Related]

  • 9. Conditional disruption of hepatic carbamoyl phosphate synthetase 1 in mice results in hyperammonemia without orotic aciduria and can be corrected by liver-directed gene therapy.
    Khoja S, Nitzahn M, Hermann K, Truong B, Borzone R, Willis B, Rudd M, Palmer DJ, Ng P, Brunetti-Pierri N, Lipshutz GS.
    Mol Genet Metab; 2018 Aug; 124(4):243-253. PubMed ID: 29801986
    [Abstract] [Full Text] [Related]

  • 10. Fatal hyperammonemia and carbamoyl phosphate synthetase 1 (CPS1) deficiency following high-dose chemotherapy and autologous hematopoietic stem cell transplantation.
    Laemmle A, Hahn D, Hu L, Rüfenacht V, Gautschi M, Leibundgut K, Nuoffer JM, Häberle J.
    Mol Genet Metab; 2015 Mar; 114(3):438-44. PubMed ID: 25639153
    [Abstract] [Full Text] [Related]

  • 11. 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; 48(4):451-5. PubMed ID: 19322055
    [Abstract] [Full Text] [Related]

  • 12. Living donor liver transplantation for pediatric patients with metabolic disorders: the Japanese multicenter registry.
    Kasahara M, Sakamoto S, Horikawa R, Koji U, Mizuta K, Shinkai M, Takahito Y, Taguchi T, Inomata Y, Uemoto S, Tatsuo K, Kato S.
    Pediatr Transplant; 2014 Feb; 18(1):6-15. PubMed ID: 24283623
    [Abstract] [Full Text] [Related]

  • 13. Model for End-Stage Liver Disease score does not predict patient or graft survival in living donor liver transplant recipients.
    Hayashi PH, Forman L, Steinberg T, Bak T, Wachs M, Kugelmas M, Everson GT, Kam I, Trotter JF.
    Liver Transpl; 2003 Jul; 9(7):737-40. PubMed ID: 12827562
    [Abstract] [Full Text] [Related]

  • 14. Live donor liver transplantation for fulminant hepatic failure in children.
    Liu CL, Fan ST, Lo CM, Tam PK, Saing H, Wei WI, Yong BH, Tsoi NS, Wong J.
    Liver Transpl; 2003 Nov; 9(11):1185-90. PubMed ID: 14586880
    [Abstract] [Full Text] [Related]

  • 15. Carbamoyl phosphate synthetase 1 deficiency in Italy: clinical and genetic findings in a heterogeneous cohort.
    Funghini S, Thusberg J, Spada M, Gasperini S, Parini R, Ventura L, Meli C, De Cosmo L, Sibilio M, Mooney SD, Guerrini R, Donati MA, Morrone A.
    Gene; 2012 Feb 10; 493(2):228-34. PubMed ID: 22173106
    [Abstract] [Full Text] [Related]

  • 16. 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 10; 13(6):848-52. PubMed ID: 17539004
    [Abstract] [Full Text] [Related]

  • 17. Living donor liver transplantation in pediatric patients with acute liver failure: safe and effective alternative.
    Uribe M, González G, Alba A, Godoy J, Ferrario M, Hunter B, Iñiguez R, Cavallieri S, Díaz V, Macho L, Ferrón S, Buckel E.
    Transplant Proc; 2008 Nov 10; 40(9):3253-5. PubMed ID: 19010246
    [Abstract] [Full Text] [Related]

  • 18. Prenatal diagnosis of carbamoyl phosphate synthetase I deficiency by identification of a missense mutation in CPS1.
    Finckh U, Kohlschütter A, Schäfer H, Sperhake K, Colombo JP, Gal A.
    Hum Mutat; 1998 Nov 10; 12(3):206-11. PubMed ID: 9711878
    [Abstract] [Full Text] [Related]

  • 19. Living liver donation: preoperative assessment, anatomic considerations, and long-term outcome.
    Chisuwa H, Hashikura Y, Mita A, Miyagawa S, Terada M, Ikegami T, Nakazawa Y, Urata K, Ogino S, Kawasaki S.
    Transplantation; 2003 May 27; 75(10):1670-6. PubMed ID: 12777854
    [Abstract] [Full Text] [Related]

  • 20. Recurrence of carbamoyl phosphate synthetase 1 (CPS1) deficiency in Turkish patients: characterization of a founder mutation by use of recombinant CPS1 from insect cells expression.
    Hu L, Diez-Fernandez C, Rüfenacht V, Hismi BÖ, Ünal Ö, Soyucen E, Çoker M, Bayraktar BT, Gunduz M, Kiykim E, Olgac A, Pérez-Tur J, Rubio V, Häberle J.
    Mol Genet Metab; 2014 Dec 27; 113(4):267-73. PubMed ID: 25410056
    [Abstract] [Full Text] [Related]

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