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
149 related items for PubMed ID: 3950131
1. Neonatal citrullinemia associated with cutaneous manifestations and arginine deficiency. Goldblum OM, Brusilow SW, Maldonado YA, Farmer ER. J Am Acad Dermatol; 1986 Feb; 14(2 Pt 2):321-6. PubMed ID: 3950131 [Abstract] [Full Text] [Related]
6. Increased urinary excretion of argininosuccinate in type II citrullinemia. Saheki T, Kobayashi K, Inoue I, Matuo S, Hagihara S, Noda T. Clin Chim Acta; 1987 Dec; 170(2-3):297-304. PubMed ID: 3436063 [Abstract] [Full Text] [Related]
7. Qualitative abnormality of liver argininosuccinate synthetase in a patient with citrullinemia. Matsuda Y, Tsuji A, Katunuma N. Adv Exp Med Biol; 1982 Dec; 153():77-82. PubMed ID: 7164924 [No Abstract] [Full Text] [Related]
9. Detection of kinetically abnormal argininosuccinate synthase in neonatal citrullinemia by conversion of citrulline to arginine in intact fibroblasts. Ben-Yoseph Y, Mitchell DA. Clin Chim Acta; 1989 Aug 15; 183(2):125-33. PubMed ID: 2791302 [Abstract] [Full Text] [Related]
10. Prospective management of a child with neonatal citrullinemia. Melnyk AR, Matalon R, Henry BW, Zeller WP, Lange C. J Pediatr; 1993 Jan 15; 122(1):96-8. PubMed ID: 8419623 [Abstract] [Full Text] [Related]
15. Periodic hyperammonemia, hyperlysinemia, and homocitrullinuria associated with decreased argininosuccinate synthetase and arginase activities. Sogawa H, Oyanagi K, Nakao T. Pediatr Res; 1977 Sep 15; 11(9 Pt 1):949-53. PubMed ID: 904980 [No Abstract] [Full Text] [Related]
16. Somatic cell genetic evidence for the presence of a gene for citrullinemia on human chromosome 9. Carritt B. Cytogenet Cell Genet; 1977 Sep 15; 19(1):44-8. PubMed ID: 891260 [No Abstract] [Full Text] [Related]
17. Citrullinemia: early diagnosis & successful management of an otherwise lethal disorder. Balsekar MV, Ambani LM, Bhatia RS, Shah SB, Apte BN. Indian Pediatr; 1989 Jun 15; 26(6):589-92. PubMed ID: 2583813 [No Abstract] [Full Text] [Related]
18. Argininosuccinic acid synthetase deficiency in a hamster cell line and its complementation of argininosuccinic aciduria human fibroblasts. González-Noriega A, Verduzco J, Prieto E, Velázquez A. J Inherit Metab Dis; 1980 Jun 15; 3(2):45-8. PubMed ID: 6777600 [Abstract] [Full Text] [Related]
19. Structure of an abnormal messenger RNA for argininosuccinate synthetase in citrullinemia. Kobayashi K, Ichiki H, Saheki T, Tatsuno M, Uchiyama C, Nukada O, Yoda T. Hum Genet; 1987 May 15; 76(1):27-32. PubMed ID: 3570300 [Abstract] [Full Text] [Related]
20. [A case of citrullinemia with fair response to oral administration of sodium benzoate for consciousness disturbance]. Wada S, Matsuo K, Nozawa K, Yazaki K, Suzuki Y, Nishizawa K, Sakai H, Huruta S. Nihon Shokakibyo Gakkai Zasshi; 1991 Sep 15; 88(9):2166-70. PubMed ID: 1795430 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]