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2. The mucopolysaccharidoses and mucolipidoses. Kelly TE Clin Orthop Relat Res; 1976; (114):116-33. PubMed ID: 131015 [TBL] [Abstract][Full Text] [Related]
3. [Genetic problems. Mucopolysaccharidoses and mucolipidoses]. Lambotte C Rev Med Liege; 1975 Nov; 30(21):751-64. PubMed ID: 812167 [No Abstract] [Full Text] [Related]
4. [Genetic, biochemical and morphopathological bases for the current classification of neurolipidoses]. Predescu V; Alexianu M; Milea S; Christodorescu D Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1977; 22(1):1-14. PubMed ID: 406655 [No Abstract] [Full Text] [Related]
13. [Fucosidosis type 2. A new case (author's transl)]. Santolaya JM; Hernández M; Chabas A; Cabello A; Rivera JM; Rodríguez MI An Esp Pediatr; 1977 Nov; 10(11):857-66. PubMed ID: 607839 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]