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Journal Abstract Search
89 related items for PubMed ID: 4789835
1. [A hereditary spastic paralysis in rabbits. II. Biochemical experiments; determination of a disorder in amino-acid metabolism]. Magnussen K. Z Morphol Anthropol; 1973 Apr; 65(1):106-21. PubMed ID: 4789835 [No Abstract] [Full Text] [Related]
2. [Familial spastic diplegia and arginemia]. Rodríguez-García A, Olmos-García de Alba G, Valarezo-Crespo F. Bol Med Hosp Infant Mex; 1982 Oct; 39(10):675-9. PubMed ID: 7171383 [No Abstract] [Full Text] [Related]
3. [Hereditary tyrosinemia. II. Presentation of a system of detection]. Bélanger M, Saint-Hilaire B. Pediatrie; 1973 Oct; 28(1):19-22. PubMed ID: 4715464 [No Abstract] [Full Text] [Related]
11. [Paper samples in detection and confirmation of some anomalies of amino acid metabolism]. Charpentier C, Lemonnier A. Ann Biol Clin (Paris); 1969 Jul; 27(5):297-323. PubMed ID: 4897889 [No Abstract] [Full Text] [Related]
12. Plasma amino acid and urine organic acid analyses of methylmalonic acidemia in a Thai infant. Srisomsap' C, Wasant P, Svasti J, Chokchaichamnankit D, Liammongkolkul S. Southeast Asian J Trop Med Public Health; 1999 Jul; 30 Suppl 2():140-2. PubMed ID: 11400752 [Abstract] [Full Text] [Related]
13. [Clinical and biochemical study of a case of histidinemia]. Beauvais P, Klein F, Humbel R, Dreyfus J, Gast. Arch Fr Pediatr; 1971 Feb; 28(2):191-203. PubMed ID: 5574024 [No Abstract] [Full Text] [Related]
14. [Personal experience in the clinical use of free amino acids in the blood and urine]. Borota J, Velisavljev M, Jojić M. Med Pregl; 1984 Feb; 37(9-10):387-91. PubMed ID: 6530984 [No Abstract] [Full Text] [Related]
15. [The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders]. Khiari D, Tebib N, Kaabachi N, Ben Dridi MF, Mebazaa A. Tunis Med; 1995 May; 73(5):159-67. PubMed ID: 9507277 [No Abstract] [Full Text] [Related]