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Journal Abstract Search

111 related items for PubMed ID: 1499142

  • 1. Oligosaccharides in (galacto)sialidosis urine.
    vanPelt J.
    Clin Chim Acta; 1992 Jun 30; 208(3):231-2. PubMed ID: 1499142
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  • 11. [Biochemical diagnosis of sialidosis in a child with a "cherry spot" in the fundus oculi as the main clinical symptom of the disease].
    Tsvetkova IV, Petushkova NA, Rozenfel'd EL, Barashnev IuI, Semiachkina AN.
    Vopr Med Khim; 1984 Jun 30; 30(5):81-3. PubMed ID: 6241373
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  • 12. Biochemical study of sialidosis type I in a Russian family.
    Tsvetkova IV, Petushkova NA, Zolotuchina TV, Kucharenko VI, Rosenfeld EL.
    J Inherit Metab Dis; 1987 Jun 30; 10(1):18-23. PubMed ID: 3106711
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  • 13. Biochemical comparison of the dysmorphic type with the normosomatic type of sialidosis.
    Kobayashi T, Goto I, Tanaka Y, Yamashita M, Kuroiwa Y.
    Clin Chim Acta; 1980 May 09; 103(3):343-7. PubMed ID: 7398077
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  • 14. [The structure of three major oligosaccharides in the urine of patients with mucolipidosis type II and with two new types of metabolic disease].
    Stecker G, Fournet B, HondiAssah T, Spik G, Montreuil J, Maroteaux P, Durand P, Farriaux JP.
    C R Acad Hebd Seances Acad Sci D; 1976 Feb 16; 282(7):671-3. PubMed ID: 817831
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  • 18. Neuraminidase deficiency presenting as non-immune hydrops fetalis.
    Beck M, Bender SW, Reiter HL, Otto W, Bässler R, Dancygier H, Gehler J.
    Eur J Pediatr; 1984 Dec 16; 143(2):135-9. PubMed ID: 6240403
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