Literature DB >> 285767

An improved thin-layer chromatographic method for urinary oligosaccharide screening.

A C Sewell.   

Abstract

A modified thin-layer chromatographic screening method is presented for the rapid diagnosis of glycoprotein storage disorders based upon excess oligosaccharide excretion. The system has been used successfully in the diagnosis of mannosidosis, GM1 gangliosidosis, mucolipidoses types I and III, aspartyl-glycosaminuria and fucosidosis.

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Year:  1979        PMID： 285767     DOI： 10.1016/0009-8981(79)90221-3

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN： 0009-8981            Impact factor:   3.786


  29 in total

1.  Comprehensive urinary screening for inborn errors of complex carbohydrate metabolism.

Authors:  A C Sewell; J Gehler; J Spranger
Journal:  Klin Wochenschr       Date:  1979-06-01

2.  Normomorphic sialidosis in two female adults with severe neurologic disease and without sialyl oligosacchariduria.

Authors:  K Harzer; M Cantz; A C Sewell; S S Dhareshwar; W Roggendorf; R W Heckl; O Schofer; R Thumler; J Peiffer; W Schlote
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

3.  Sialuria: a second case.

Authors:  B Wilcken; N Don; R Greenaway; J Hammond; L Sosula
Journal:  J Inherit Metab Dis       Date:  1987       Impact factor: 4.982

4.  Urinary screening for disorders of heteroglycan metabolism. Results of 10 years experience with a comprehensive system.

Authors:  A C Sewell
Journal:  Klin Wochenschr       Date:  1988-01-15

5.  The simple detection of neuraminic acid-containing urinary oligosaccharides in patients with glycoprotein storage diseases.

Authors:  A C Sewell
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

6.  Absence of alpha-fucosidase activity in two sisters showing a different phenotype.

Authors:  H Christomanou; D Beyer
Journal:  Eur J Pediatr       Date:  1983-03       Impact factor: 3.183

Review 7.  Aspartylglycosaminuria: an inborn error of glycoprotein catabolism.

Authors:  C P Maury
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

8.  Prenatal diagnosis of GM1 gangliosidosis by detection of galactosyl-oligosaccharides in amniotic fluid with high-performance liquid chromatography.

Authors:  T G Warner; A D Robertson; A K Mock; W G Johnson; J S O'Brien
Journal:  Am J Hum Genet       Date:  1983-09       Impact factor: 11.025

9.  Chemical chaperone therapy for brain pathology in G(M1)-gangliosidosis.

Authors:  Junichiro Matsuda; Osamu Suzuki; Akihiro Oshima; Yoshie Yamamoto; Akira Noguchi; Kazuhiro Takimoto; Masayuki Itoh; Yuji Matsuzaki; Yosuke Yasuda; Seiichiro Ogawa; Yuko Sakata; Eiji Nanba; Katsumi Higaki; Yoshimi Ogawa; Lika Tominaga; Kousaku Ohno; Hiroyuki Iwasaki; Hiroshi Watanabe; Roscoe O Brady; Yoshiyuki Suzuki
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-15       Impact factor: 11.205

10.  Amniotic fluid glycoasparagines in fetal aspartylglycosaminuria.

Authors:  I Mononen; V Kaartinen; T Mononen
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982
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