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Journal Abstract Search

226 related items for PubMed ID: 6775948

  • 21. Abnormal urinary oligosaccharide pattern in patients with glycogen storage disease, type III.
    McLaren J, Ng WG, Roe T.
    Clin Chem; 1980 Dec; 26(13):1924-5. PubMed ID: 6934040
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  • 24. [Structures of 9 oligosaccharides and glycopeptides containing large amounts of fucose excreted in the urine of 2 patients with fucosidosis].
    Strecker G, Fournet B, Spik G, Montreuil J, Durand P, Tondeur M.
    C R Acad Hebd Seances Acad Sci D; 1977 Jan 03; 284(1):85-8. PubMed ID: 402234
    [No Abstract] [Full Text] [Related]

  • 25. Oligosaccharides from human urine.
    Lundblad A.
    Methods Enzymol; 1978 Jan 03; 50():226-35. PubMed ID: 96316
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  • 27. A capillary electrophoresis procedure for the screening of oligosaccharidoses and related diseases.
    Casado M, Altimira L, Montero R, Castejón E, Nascimento A, Pérez-Dueñas B, Ormazabal A, Artuch R.
    Anal Bioanal Chem; 2014 Jul 03; 406(18):4337-43. PubMed ID: 24788891
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  • 28. Rapid ultraperformance liquid chromatography-tandem mass spectrometry assay for a characteristic glycogen-derived tetrasaccharide in Pompe disease and other glycogen storage diseases.
    Sluiter W, van den Bosch JC, Goudriaan DA, van Gelder CM, de Vries JM, Huijmans JG, Reuser AJ, van der Ploeg AT, Ruijter GJ.
    Clin Chem; 2012 Jul 03; 58(7):1139-47. PubMed ID: 22623745
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  • 29. Urinary oligosaccharide excretion in nephrotic syndrome.
    Takahashi Y, Omiya S, Nakamura Y, Kondo N, Orii T.
    Pediatr Res; 1993 Oct 03; 34(4):429-34. PubMed ID: 8255672
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  • 30. Interference of amikacin in thin-layer chromatographic screening of urine for oligosaccharidosis.
    Piraud M, Maire I.
    Clin Chem; 1990 May 03; 36(5):809. PubMed ID: 2337995
    [No Abstract] [Full Text] [Related]

  • 31. [Hereditary diseases connected with defective metabolism of polysaccharides and mixed carbohydrate-containing biopolymers].
    Rozenfel'd EL.
    Vestn Akad Med Nauk SSSR; 1973 May 03; 28(1):74-81. PubMed ID: 4203774
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  • 32. The pseudo-Hurler syndromes.
    Gordon N.
    Dev Med Child Neurol; 1978 Jun 03; 20(3):383-7. PubMed ID: 97112
    [No Abstract] [Full Text] [Related]

  • 33. The storage products in genetic and swainsonine-induced human mannosidosis.
    Cenci di Bello I, Dorling P, Winchester B.
    Biochem J; 1983 Dec 01; 215(3):693-6. PubMed ID: 6419731
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  • 34. Increased urinary excretion of a glycogen-derived tetrasaccharide in heterozygotes with glycogen storage diseases type II and III.
    Chester MA, Lundblad A, Häger A, Sjöblad S, Loonen C, Tager JM, Zopf D.
    Lancet; 1983 Apr 30; 1(8331):994-5. PubMed ID: 6132305
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  • 35. The genetic mucolipidoses. Diagnosis and differential diagnosis.
    Spranger JW, Wiedemann HR.
    Humangenetik; 1970 Apr 30; 9(2):113-39. PubMed ID: 4246487
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  • 37. Mannosidosis: isolation and comparison of mannose-containing oligosaccharides from gingiva and urine.
    Daniel PF, Defeudis DF, Lott IT.
    Eur J Biochem; 1981 Feb 30; 114(2):235-7. PubMed ID: 7215354
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  • 39. Urinary oligosaccharide screening detects type VI glycogen storage disease.
    Sewell AC.
    Clin Chem; 1986 Feb 30; 32(2):392. PubMed ID: 3455896
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  • 40. Analysis of urinary oligosaccharide excretion patterns by UHPLC/HRAM mass spectrometry for screening of lysosomal storage disorders.
    Hagemeijer MC, van den Bosch JC, Bongaerts M, Jacobs EH, van den Hout JMP, Oussoren E, Ruijter GJG.
    J Inherit Metab Dis; 2023 Mar 30; 46(2):206-219. PubMed ID: 36752951
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