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13. Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristics. Gehler J; Sewell AC; Becker C; Spranger J; Hartmann J J Inherit Metab Dis; 1981; 4(4):229-30. PubMed ID: 6796777 [TBL] [Abstract][Full Text] [Related]
14. Characterization of the storage material of peripheral lymphocytes in aspartylglycosaminuria. Maury P; Palo J Clin Sci (Lond); 1980 Feb; 58(2):165-8. PubMed ID: 7357836 [TBL] [Abstract][Full Text] [Related]
15. Elevated levels of serum dolichol in aspartylglucosaminuria. Salaspuro M; Salmela K; Humaloja K; Autio S; Arvio M; Palo J Life Sci; 1990; 47(7):627-32. PubMed ID: 2402187 [TBL] [Abstract][Full Text] [Related]
16. Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian family. Gehler J; Sewell AC; Becker C; Hartmann J; Spranger J Helv Paediatr Acta; 1981; 36(2):179-89. PubMed ID: 6788730 [TBL] [Abstract][Full Text] [Related]
17. Abnormal collagen fibrils in aspartylglycosaminuria. Altered dermal ultrastructure in a glycoprotein storage disorder. Näntö-Salonen K; Pelliniemi LJ; Autio S; Kivimäki T; Rapola J; Penttinen R Lab Invest; 1984 Oct; 51(4):464-8. PubMed ID: 6592395 [TBL] [Abstract][Full Text] [Related]
18. 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]