{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,9,10]],"date-time":"2024-09-10T21:51:56Z","timestamp":1726005116720},"reference-count":27,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[1983,3,30]],"date-time":"1983-03-30T00:00:00Z","timestamp":417830400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Inher Metab Disea"],"published-print":{"date-parts":[[1983,12]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Urine samples from patients with different types of glycoprotein storage disease were chromatographed by gel filtration and the fractions analysed for sialic acid. Patients with mucolipidoses I and II excreted the largest amounts of bound sialic acid. One patient with GM<jats:sub>1<\/jats:sub> gangliosidosis showed an abnormal level of sialyloligosaccharide excretion. Other patients showed normal results. With the present method mucolipidoses I and II, together with GM<jats:sub>1<\/jats:sub> gangliosidosis, are readily distinguished from other possible oligosaccharidurias.<\/jats:p>","DOI":"10.1007\/bf02310870","type":"journal-article","created":{"date-parts":[[2006,2,15]],"date-time":"2006-02-15T15:54:22Z","timestamp":1140018862000},"page":"153-157","source":"Crossref","is-referenced-by-count":3,"title":["The simple detection of neuraminic acid\u2010containing urinary oligosaccharides in patients with glycoprotein storage diseases"],"prefix":"10.1002","volume":"6","author":[{"given":"A. C.","family":"Sewell","sequence":"first","affiliation":[{"name":"Department of Biochemistry Royal Gwent Hospital  Newport Gwent NPT 2UB"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[1983,3,30]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/0006-291X(79)91183-5"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF02179146"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1016\/0006-291X(77)90363-1"},{"key":"e_1_2_1_5_1","doi-asserted-by":"publisher","DOI":"10.1093\/clinchem\/24.9.1576"},{"key":"e_1_2_1_6_1","first-page":"179","article-title":"Clinical and biochemical delineation of aspartylglycosaminuria as observed in two members of an Italian family","volume":"36","author":"Gehler J.","year":"1981","journal-title":"Helv. Paediatr. Acta"},{"key":"e_1_2_1_7_1","first-page":"258","article-title":"Morquio syndrome (mucopolysaccharidosis IVB) associated with \u03b2\u2010galactosidase deficiency. Report of two cases","volume":"32","author":"Gr\u00f6be H.","year":"1980","journal-title":"Am. J. Hum. Genet."},{"key":"e_1_2_1_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/0009-8981(75)90119-9"},{"key":"e_1_2_1_9_1","doi-asserted-by":"publisher","DOI":"10.1203\/00006450-197210000-00002"},{"key":"e_1_2_1_10_1","first-page":"1","article-title":"Sialidosis: a review of human neuraminidase deficiency","volume":"31","author":"Lowden J. A.","year":"1979","journal-title":"Am. J. Hum. Genet."},{"key":"e_1_2_1_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/B978-0-12-356101-5.50026-2"},{"key":"e_1_2_1_12_1","doi-asserted-by":"publisher","DOI":"10.1016\/0009-8981(81)90337-5"},{"key":"e_1_2_1_13_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1978.tb02061.x"},{"key":"e_1_2_1_14_1","doi-asserted-by":"publisher","DOI":"10.3891\/acta.chem.scand.21-1670"},{"key":"e_1_2_1_15_1","doi-asserted-by":"publisher","DOI":"10.1016\/0009-8981(78)90129-8"},{"key":"e_1_2_1_16_1","doi-asserted-by":"publisher","DOI":"10.1002\/ana.410030309"},{"key":"e_1_2_1_17_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0021-9258(18)71120-4"},{"key":"e_1_2_1_18_1","doi-asserted-by":"publisher","DOI":"10.1016\/0009-8981(79)90221-3"},{"key":"e_1_2_1_19_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00496087"},{"key":"e_1_2_1_20_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320010104"},{"key":"e_1_2_1_21_1","first-page":"13","volume-title":"Les Oligosaccharidoses","author":"Strecker G.","year":"1977"},{"key":"e_1_2_1_22_1","doi-asserted-by":"publisher","DOI":"10.1016\/0014-5793(78)81239-3"},{"key":"e_1_2_1_23_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1432-1033.1977.tb11540.x"},{"key":"e_1_2_1_24_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00273261"},{"key":"e_1_2_1_25_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1471-4159.1963.tb08933.x"},{"key":"e_1_2_1_26_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1979.tb01010.x"},{"key":"e_1_2_1_27_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0021-9258(18)69851-5"},{"key":"e_1_2_1_28_1","doi-asserted-by":"publisher","DOI":"10.1016\/0006-291X(78)90915-4"}],"container-title":["Journal of Inherited Metabolic Disease"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1007\/BF02310870","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1007\/BF02310870","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,16]],"date-time":"2023-09-16T05:47:30Z","timestamp":1694843250000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1007\/BF02310870"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1983,3,30]]},"references-count":27,"journal-issue":{"issue":"4","published-print":{"date-parts":[[1983,12]]}},"alternative-id":["10.1007\/BF02310870"],"URL":"https:\/\/doi.org\/10.1007\/bf02310870","archive":["Portico"],"relation":{},"ISSN":["0141-8955","1573-2665"],"issn-type":[{"value":"0141-8955","type":"print"},{"value":"1573-2665","type":"electronic"}],"subject":[],"published":{"date-parts":[[1983,3,30]]}}}