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2. [Aspartylglucosaminuria. A hereditary disease with unusual high incidence among Finns in northern Norway]. Torp KH; Borud O Tidsskr Nor Laegeforen; 1978 Aug; 98(24):1145-6. PubMed ID: 684720 [No Abstract] [Full Text] [Related]
5. Aspartylglycosaminuria in Northern Norway in eight patients: clinical heterogeneity and variations with the diet. Borud O; Strömme JH; Lie SO; Torp KH J Inherit Metab Dis; 1978; 1(3):95-7. PubMed ID: 116085 [TBL] [Abstract][Full Text] [Related]
6. Recent findings on some "new" neurometabolic diseases. Palo J; Santavuori P; Haltia M Riv Patol Nerv Ment; 1976 Aug; 97(4):191-8. PubMed ID: 1032035 [TBL] [Abstract][Full Text] [Related]
7. N-Acetylglucosamine-asparagine levels in tissues of patients with aspartylglycosaminuria. Maury CP; Palo J Clin Chim Acta; 1980 Dec; 108(2):293-9. PubMed ID: 7449147 [TBL] [Abstract][Full Text] [Related]
8. Extra heating of TLC plates detects two lysosomal storage diseases, aspartylglucosaminuria and fucosidosis, during routine urinary amino acid screening. Simell O; Sipilä I; Autio S Clin Chim Acta; 1983 Sep; 133(2):227-32. PubMed ID: 6627685 [No Abstract] [Full Text] [Related]
9. Copper and zinc metabolism in aspartylglycosaminuria and Salla disease. van Langevelde F; Vis RD; Näntö-Salonen K; Halme T; Pakarinen P; Hyörä H; Vuorinen K; Näntö V Sci Total Environ; 1985 Mar; 42(1-2):171-80. PubMed ID: 4012278 [TBL] [Abstract][Full Text] [Related]
10. Aspartylglucosaminuria in the United States. Hreidarsson S; Thomas GH; Valle DL; Stevenson RE; Taylor H; McCarty J; Coker SB; Green WR Clin Genet; 1983 Jun; 23(6):427-35. PubMed ID: 6883788 [TBL] [Abstract][Full Text] [Related]