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Journal Abstract Search
176 related items for PubMed ID: 12370774
1. Progressive liver fibrosis in late-onset argininosuccinate lyase deficiency. Mori T, Nagai K, Mori M, Nagao M, Imamura M, Iijima M, Kobayashi K. Pediatr Dev Pathol; 2002; 5(6):597-601. PubMed ID: 12370774 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
3. 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 [Abstract] [Full Text] [Related]
4. [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 [Abstract] [Full Text] [Related]
13. Argininosuccinate lyase deficiency: mutational spectrum in Italian patients and identification of a novel ASL pseudogene. Trevisson E, Salviati L, Baldoin MC, Toldo I, Casarin A, Sacconi S, Cesaro L, Basso G, Burlina AB. Hum Mutat; 2007 Jul; 28(7):694-702. PubMed ID: 17326097 [Abstract] [Full Text] [Related]
14. Hereditary urea cycle diseases in Finland. Keskinen P, Siitonen A, Salo M. Acta Paediatr; 2008 Oct; 97(10):1412-9. PubMed ID: 18616627 [Abstract] [Full Text] [Related]