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Journal Abstract Search

243 related items for PubMed ID: 16618422

  • 1. Sustained engraftment and tissue enzyme activity after liver cell transplantation for argininosuccinate lyase deficiency.
    Stéphenne X, Najimi M, Sibille C, Nassogne MC, Smets F, Sokal EM.
    Gastroenterology; 2006 Apr; 130(4):1317-23. PubMed ID: 16618422
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  • 3. [Argininosuccinic aciduria. A new case revealed by psychiatric disorders].
    Odent S, Roussey M, Journel H, Betremieux P, David V, Le Marec B.
    J Genet Hum; 1989 Jan; 37(1):39-42. PubMed ID: 2715782
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  • 5. Severe liver fibrosis in argininosuccinic aciduria.
    Zimmermann A, Bachmann C, Baumgartner R.
    Arch Pathol Lab Med; 1986 Feb; 110(2):136-40. PubMed ID: 3753845
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  • 6. [Argininosuccinate lyase deficiency].
    Matsubasa T.
    Ryoikibetsu Shokogun Shirizu; 1998 Feb; (18 Pt 1):179-81. PubMed ID: 9590021
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  • 7. Use of amniotic fluid amino acids in prenatal testing for argininosuccinic aciduria and citrullinaemia.
    Mandell R, Packman S, Laframboise R, Golbus MS, Schmidt K, Workman L, Saudubray JM, Shih VE.
    Prenat Diagn; 1996 May; 16(5):419-24. PubMed ID: 8843999
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  • 8. Argininosuccinate lyase deficiency (ASL) and carbohydrate-deficient transferrin (CDT): experience with four independent CDT analysis methods--misleading results given by the %CDT TIA assay.
    Arndt T, Gressner A, Herwig J, Meier U, Sewell AC.
    Clin Chim Acta; 2006 Nov; 373(1-2):117-20. PubMed ID: 16808909
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  • 9. Liver cell transplantation.
    Najimi M, Sokal E.
    Minerva Pediatr; 2005 Oct; 57(5):243-57. PubMed ID: 16205608
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  • 10. Long-term follow-up of 12 patients with the late-onset variant of argininosuccinic acid lyase deficiency: no impairment of intellectual and psychomotor development during therapy.
    Widhalm K, Koch S, Scheibenreiter S, Knoll E, Colombo JP, Bachmann C, Thalhammer O.
    Pediatrics; 1992 Jun; 89(6 Pt 2):1182-4. PubMed ID: 1594374
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  • 11. 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 15; 87(5):636-41. PubMed ID: 19295306
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  • 12. [State of hepatocyte transplantation: a risk or a chance?].
    Leckel K, Blaheta RA, Markus BH.
    Zentralbl Chir; 2003 Apr 15; 128(4):283-90. PubMed ID: 12700984
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  • 13. Argininosuccinic aciduria: clinical and biochemical phenotype findings in Malaysian children.
    Chen BC, Ngu LH, Zabedah MY.
    Malays J Pathol; 2010 Dec 15; 32(2):87-95. PubMed ID: 21329179
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  • 14. Dietary management reverses grooving and abnormal polarization of hair shafts in argininosuccinase deficiency.
    Kvedar JC, Baden HP, Baden LA, Shih VE, Kolodny EH.
    Am J Med Genet; 1991 Aug 01; 40(2):211-3. PubMed ID: 1897577
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  • 15. Management of hyperbilirubinemia in biliary atresia by hepatic progenitor cell transplantation through hepatic artery: a case report.
    Khan AA, Parveen N, Mahaboob VS, Rajendraprasad A, Ravindraprakash HR, Venkateswarlu J, Rao P, Pande G, Narusu ML, Khaja MN, Pramila R, Habeeb A, Habibullah CM.
    Transplant Proc; 2008 May 01; 40(4):1153-5. PubMed ID: 18555137
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  • 18. [Argininosuccinic aciduria].
    Kobayashi K, Tatsuno M, Matuo S, Saheki T.
    Tanpakushitsu Kakusan Koso; 1988 Apr 01; 33(5):510-3. PubMed ID: 3270856
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  • 19. Two novel mutations (E86A, R113W) in argininosuccinate lyase deficiency and evidence for highly variable splicing of the human argininosuccinate lyase gene.
    Linnebank M, Homberger A, Rapp B, Winter C, Marquardt T, Harms E, Koch HG.
    J Inherit Metab Dis; 2000 Jun 01; 23(4):308-12. PubMed ID: 10896281
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  • 20. Citrate therapy in argininosuccinate lyase deficiency.
    Iafolla AK, Gale DS, Roe CR.
    J Pediatr; 1990 Jul 01; 117(1 Pt 1):102-5. PubMed ID: 2370602
    [No Abstract] [Full Text] [Related]

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