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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

439 related articles for article (PubMed ID: 26640932)

  • 1. Report of 3 Patients With Urea Cycle Defects Treated With Related Living-Donor Liver Transplant.
    Özçay F; Barış Z; Moray G; Haberal N; Torgay A; Haberal M
    Exp Clin Transplant; 2015 Nov; 13 Suppl 3():126-30. PubMed ID: 26640932
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Argininosuccinic Aciduria-A Rare Indication for Liver Transplant: Report of Two Cases.
    Yankol Y; Mecit N; Kanmaz T; Acarli K; Kalayoglu M
    Exp Clin Transplant; 2017 Oct; 15(5):581-584. PubMed ID: 26768012
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Urea cycle disorders in Argentine patients: clinical presentation, biochemical and genetic findings.
    Silvera-Ruiz SM; Arranz JA; Häberle J; Angaroni CJ; Bezard M; Guelbert N; Becerra A; Peralta F; de Kremer RD; Laróvere LE
    Orphanet J Rare Dis; 2019 Aug; 14(1):203. PubMed ID: 31426867
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Urea cycle disorders in Thai infants: a report of 5 cases.
    Wasant P; Srisomsap C; Liammongkolkul S; Svasti J
    J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S720-31. PubMed ID: 12403252
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Curative Treatment of Ornithine Transcarbamylase Deficiency With a Liver Transplant: A Case Report.
    Shamsaeefar A; Nikeghbalian S; Dehghani SM; Kazemi K; Motazedian N; Geramizadeh B; Malekhosseini SA
    Exp Clin Transplant; 2019 Feb; 17(1):119-120. PubMed ID: 27447480
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Histopathological findings in livers of patients with urea cycle disorders.
    Yaplito-Lee J; Chow CW; Boneh A
    Mol Genet Metab; 2013 Mar; 108(3):161-5. PubMed ID: 23403242
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hereditary urea cycle diseases in Finland.
    Keskinen P; Siitonen A; Salo M
    Acta Paediatr; 2008 Oct; 97(10):1412-9. PubMed ID: 18616627
    [TBL] [Abstract][Full Text] [Related]  

  • 9. One liver for four children: first clinical series of liver cell transplantation for severe neonatal urea cycle defects.
    Meyburg J; Das AM; Hoerster F; Lindner M; Kriegbaum H; Engelmann G; Schmidt J; Ott M; Pettenazzo A; Luecke T; Bertram H; Hoffmann GF; Burlina A
    Transplantation; 2009 Mar; 87(5):636-41. PubMed ID: 19295306
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical course of 63 patients with neonatal onset urea cycle disorders in the years 2001-2013.
    Unsinn C; Das A; Valayannopoulos V; Thimm E; Beblo S; Burlina A; Konstantopoulou V; Mayorandan S; de Lonlay P; Rennecke J; Derbinski J; Hoffmann GF; Häberle J
    Orphanet J Rare Dis; 2016 Aug; 11(1):116. PubMed ID: 27538463
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hyperammonemia in ornithine transcarbamylase-deficient recipients following living donor liver transplantation from heterozygous carrier donors.
    Rahayatri TH; Uchida H; Sasaki K; Shigeta T; Hirata Y; Kanazawa H; Mali V; Fukuda A; Sakamoto S; Kasahara M
    Pediatr Transplant; 2017 Feb; 21(1):. PubMed ID: 27891735
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Liver transplantation in urea cycle disorders.
    Saudubray JM; Touati G; Delonlay P; Jouvet P; Narcy C; Laurent J; Rabier D; Kamoun P; Jan D; Revillon Y
    Eur J Pediatr; 1999 Dec; 158 Suppl 2():S55-9. PubMed ID: 10603100
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal treatment of ornithine transcarbamylase deficiency.
    Wilnai Y; Blumenfeld YJ; Cusmano K; Hintz SR; Alcorn D; Benitz WE; Berquist WE; Bernstein JA; Castillo RO; Concepcion W; Cowan TM; Cox KL; Lyell DJ; Esquivel CO; Homeyer M; Hudgins L; Hurwitz M; Palma JP; Schelley S; Akula VP; Summar ML; Enns GM
    Mol Genet Metab; 2018 Mar; 123(3):297-300. PubMed ID: 29396029
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Anesthesia management protocol for liver transplantation as treatment for ornithine transcarbamylase deficiency.
    Baba C; Yukimasa S; Yasuno R; Ichiyanagi H; Ninagawa J; Kasuya S; Kasahara M; Horikawa R; Nagasaka Y; Suzuki Y
    Paediatr Anaesth; 2023 Aug; 33(8):620-630. PubMed ID: 37401903
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prospective treatment of urea cycle disorders.
    Maestri NE; Hauser ER; Bartholomew D; Brusilow SW
    J Pediatr; 1991 Dec; 119(6):923-8. PubMed ID: 1720458
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Urea cycle disorders in India: clinical course, biochemical and genetic investigations, and prenatal testing.
    Bijarnia-Mahay S; Häberle J; Jalan AB; Puri RD; Kohli S; Kudalkar K; Rüfenacht V; Gupta D; Maurya D; Verma J; Shigematsu Y; Yamaguchi S; Saxena R; Verma IC
    Orphanet J Rare Dis; 2018 Oct; 13(1):174. PubMed ID: 30285816
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Citrullinemia Type 1: Behavioral Improvement with Late Liver Transplantation.
    Janwadkar A; Shirole N; Nagral A; Bakshi R; Vasanth S; Bagde A; Yewale V; Mirza D
    Indian J Pediatr; 2019 Jul; 86(7):639-641. PubMed ID: 30848473
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Argininosuccinate lyase deficiency-argininosuccinic aciduria and beyond.
    Erez A; Nagamani SC; Lee B
    Am J Med Genet C Semin Med Genet; 2011 Feb; 157C(1):45-53. PubMed ID: 21312326
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Argininosuccinate lyase deficiency.
    Nagamani SC; Erez A; Lee B
    Genet Med; 2012 May; 14(5):501-7. PubMed ID: 22241104
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.