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Journal Abstract Search
162 related items for PubMed ID: 4370029
1. Fructose-1,6-diphosphatase deficiency: another enzyme defect which can present itself with the clinical features of "tyrosinosis". Bakker HD, de Bree PK, van Sprang FJ, Wadman SK. Clin Chim Acta; 1974 Aug 30; 55(1):41-7. PubMed ID: 4370029 [No Abstract] [Full Text] [Related]
4. Detection of fructose-1,6-diphosphatase deficiency with use of white blood cells. Melancon SB, Nadler HL. N Engl J Med; 1972 Mar 30; 286(13):731-2. PubMed ID: 4334313 [No Abstract] [Full Text] [Related]
12. [Lactic acidosis, hypoglycemia and hepatomegaly due to hereditary defect in hepatic fructose-1, 6-diphosphatase]. Saudubray JM, Dreyfus JC, Cepanec C, Le Lo'ch H, Trung PH, Mozziconacci P. Arch Fr Pediatr; 1973 Jul 30; 30(6):609-32. PubMed ID: 4156164 [No Abstract] [Full Text] [Related]
13. [Hypertyrosinemia with hypermethioninemia in the newborn in a case of fructose intolerance]. Willems C, Heusden A, Renson P, Legat C, Monard Y, Stainier L. Helv Paediatr Acta; 1971 Oct 30; 26(4):467-81. PubMed ID: 5123311 [No Abstract] [Full Text] [Related]
14. Biochemical studies in a patient with "tyrosinosis". Louis WJ, Pitt DD, Davies H. Aust N Z J Med; 1974 Jun 30; 4(3):281-6. PubMed ID: 4531904 [No Abstract] [Full Text] [Related]
15. Infantile lactic acidosis due to hereditary fructose 1,6-diphosphatase deficiency. Baerlocher K, Gitzelmann R, Nüssli R, Dumermuth G. Helv Paediatr Acta; 1971 Dec 30; 26(5):489-506. PubMed ID: 4335192 [No Abstract] [Full Text] [Related]
16. Recovery after dietary treatment of an infant with features of tyrosinosis. Harries JT, Seakins JW, Ersser RS, Lloyd JK. Arch Dis Child; 1969 Apr 30; 44(234):258-67. PubMed ID: 5779435 [No Abstract] [Full Text] [Related]
17. Recurrent attacks of ketotic acidosis associated with fructose-1,6-diphosphatase deficiency. Corbeel L, Eggermont E, Eeckels R, Jaeken J, Casteels-Van Daele M, Devlieger H, Delmontte B. Acta Paediatr Belg; 1976 Apr 30; 29(1):29-34. PubMed ID: 189564 [No Abstract] [Full Text] [Related]
18. An exceptional case of tyrosinosis. Wadman SK, van Sprang FJ, Maas JW, Ketting D. J Ment Defic Res; 1968 Dec 30; 12(4):269-81. PubMed ID: 5729527 [No Abstract] [Full Text] [Related]
19. [Differential diagnosis between hereditary fructose intolerance and fructose-1,6-diphosphatase deficiency]. Méndez Aparicio FM. Rev Clin Esp; 1968 Dec 30; 161(5-6):289-96. PubMed ID: 6270745 [No Abstract] [Full Text] [Related]
20. Detection of heterozygotes for fructose 1,6-diphosphatase deficiency by measuring fructose 1,6-diphosphatase activity in their cultured peripheral lymphocytes. Ito M, Kuroda Y, Kobashi H, Watanabe T, Takeda E, Toshima K, Miyao M. Clin Chim Acta; 1984 Aug 15; 141(1):27-32. PubMed ID: 6088124 [Abstract] [Full Text] [Related] Page: [Next] [New Search]