244 related articles for article (PubMed ID: 27342998)
1. Amniotic fluid glycosaminoglycans in the prenatal diagnosis of mucopolysaccharidoses - A useful biomarker.
Akella RR; Kadali S
Clin Chim Acta; 2016 Sep; 460():63-6. PubMed ID: 27342998
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of mucopolysaccharidoses type II by two-dimensional electrophoresis and mass spectrometry in amniotic fluid.
Aboulnasr AA; Elnouri A; Abdel Sameea G; Gouda AS; Ibrahim MM; Shalabi TA; Gaber KR
J Obstet Gynaecol Res; 2022 Mar; 48(3):682-687. PubMed ID: 35026871
[TBL] [Abstract][Full Text] [Related]
3. An improved determination of total glycosaminoglycans in body fluids by formation of complexes with quinacrine: changes in amniotic fluid total glycosaminoglycans during normal pregnancies and in pregnancies at risk for mucopolysaccharidoses.
Mitra SK; Blau K
Clin Chim Acta; 1978 Oct; 89(1):127-34. PubMed ID: 101319
[TBL] [Abstract][Full Text] [Related]
4. A method for the determination of amniotic-fluid glycosaminoglycans and its application to the prenatal diagnosis of Hurler and Sanfilippo diseases.
Whiteman P; Henderson H
Clin Chim Acta; 1977 Aug; 79(1):99-105. PubMed ID: 408055
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of mucopolysaccharidosis by two-dimensional electrophoresis of amniotic fluid glycosaminoglycans.
Mossman J; Patrick AD
Prenat Diagn; 1982 Jul; 2(3):169-76. PubMed ID: 6815629
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of mucopolysaccharidoses (MPS): the first Egyptian experience.
Aboul Nasr A; Fateen E
Bratisl Lek Listy; 2004; 105(9):310-4. PubMed ID: 15633892
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of mucopolysaccharidosis by continuous, monodimensional electrophoresis of amniotic fluid glycosaminoglycans.
Sun NH; Wang FY; Wu YC; Ning Y
Chin Med J (Engl); 1991 Dec; 104(12):1022-4. PubMed ID: 1782812
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of Sanfilippo disease type B.
Kleijer WJ; Huijmans JG; Blom W; Gorska D; Kubalska J; Walasek M; Zaremba J
Hum Genet; 1984; 66(4):287-8. PubMed ID: 6427096
[TBL] [Abstract][Full Text] [Related]
9. Prenatal tests for Sanfilippo disease type B in four pregnancies.
Mossman J; Young EP; Patrick AD; Fensom AH; Ellis M; Benson PF; Der Kaloustian VM
Prenat Diagn; 1983 Oct; 3(4):347-50. PubMed ID: 6419220
[TBL] [Abstract][Full Text] [Related]
10. Glycosaminoglycan accumulation and excretion in the mucopolysaccharidoses: characterization and basis of a diagnostic test for MPS.
Byers S; Rozaklis T; Brumfield LK; Ranieri E; Hopwood JJ
Mol Genet Metab; 1998 Dec; 65(4):282-90. PubMed ID: 9889015
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of mucolipidosis II (I-cell disease).
Gehler J; Cantz M; Stoeckenius M; Spranger J
Eur J Pediatr; 1976 Jun; 122(3):201-6. PubMed ID: 819273
[TBL] [Abstract][Full Text] [Related]
12. The early laboratory diagnosis of mucopolysaccharidoses.
Lorincz AE; Hurst RE; Kolodny EH
Ann Clin Lab Sci; 1982; 12(4):258-66. PubMed ID: 6814341
[No Abstract] [Full Text] [Related]
13. Glycosaminoglycan levels in dried blood spots of patients with mucopolysaccharidoses and mucolipidoses.
Kubaski F; Suzuki Y; Orii K; Giugliani R; Church HJ; Mason RW; Dũng VC; Ngoc CT; Yamaguchi S; Kobayashi H; Girisha KM; Fukao T; Orii T; Tomatsu S
Mol Genet Metab; 2017 Mar; 120(3):247-254. PubMed ID: 28065440
[TBL] [Abstract][Full Text] [Related]
14. [Postnatal and prenatal diagnosis of mucopolysaccharidosis type II (Hunter syndrome)].
Zhang WM; Shi HP; Li BT; Zhao SM; Qi QW; Sun NH; Huang SZ
Zhonghua Er Ke Za Zhi; 2006 Sep; 44(9):644-7. PubMed ID: 17217652
[TBL] [Abstract][Full Text] [Related]
15. Rapid prenatal testing for human beta-glucuronidase deficiency (MPS VII).
Natowicz MR; Isman F; Prence EM; Cedrone P; Allen JJ
Genet Test; 2003; 7(3):241-3. PubMed ID: 14642000
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of the Hunter syndrome and the introduction of a new fluorimetric enzyme assay.
Keulemans JL; Sinigerska I; Garritsen VH; Huijmans JG; Voznyi YV; van Diggelen OP; Kleijer WJ
Prenat Diagn; 2002 Nov; 22(11):1016-21. PubMed ID: 12424767
[TBL] [Abstract][Full Text] [Related]
17. Postnatal and prenatal diagnosis of Maroteaux-Lamy syndrome.
Rogoyski A; Czartoryska B; Kleijer WJ; Niermeijer MF; Tronowska TD; Gorska D; Polatynska-Krzyspiak B; Zaremba J
Acta Anthropogenet; 1985; 9(1-3):109-16. PubMed ID: 3939668
[TBL] [Abstract][Full Text] [Related]
18. Diagnostic screening for mucopolysaccharidoses by the dimethylmethylene blue method and two dimensional electrophoresis.
Chuang CK; Lin SP; Chung SF
Zhonghua Yi Xue Za Zhi (Taipei); 2001 Jan; 64(1):15-22. PubMed ID: 11310367
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of Hunter syndrome.
Archer IM; Kingston HM; Harper PS
Prenat Diagn; 1984; 4(3):195-200. PubMed ID: 6431402
[TBL] [Abstract][Full Text] [Related]
20. Glycosaminoglycan analysis in amniotic fluid and in cultured fibroblasts from normal and holoprosencephalic human embryonic organs.
Stabellini G; Del Borrello E; De Mattei M; Calastrini C; Orsini LF; Franchina M
Prenat Diagn; 1997 Nov; 17(11):1077-80. PubMed ID: 9399358
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
