177 related articles for article (PubMed ID: 1527990)
1. Prenatal diagnosis of Hurler disease by analysis of alpha-iduronidase in chorionic villi.
Young EP
J Inherit Metab Dis; 1992; 15(2):224-30. PubMed ID: 1527990
[TBL] [Abstract][Full Text] [Related]
2. Use of 4-trifluoromethylumbelliferyl-alpha-L-iduronide as a new substrate for detection of alpha-L-iduronidase deficiency in human tissues and for rapid prenatal diagnosis of Hurler disease.
Tsvetkova IV; Karpova EA; Voznyi YV; Zolotukhina TV; Biryukov VV; Semyachkina AN
J Inherit Metab Dis; 1991; 14(2):134-9. PubMed ID: 1909400
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of the Hurler syndrome: report on 40 pregnancies at risk.
Kleijer WJ; Thompson EJ; Niermeijer MF
Prenat Diagn; 1983 Jul; 3(3):179-86. PubMed ID: 6413967
[TBL] [Abstract][Full Text] [Related]
4. Antenatal diagnosis of mucopolysaccharidosis type I (Hurler's disease) is not possible by electron microscopy of uncultured amniotic fluid cells.
Hug G; Soukup S; Chuck G; Ryan M
J Med Genet; 1984 Oct; 21(5):359-63. PubMed ID: 6438322
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. Correct prenatal diagnosis of a Hurler fetus where amniotic fluid cell cultures were of maternal origin.
Mossman J; Patrick AD; Fensom AH; Tansley LR; Benson PF; Der Kaloustian VM; Dudin G
Prenat Diagn; 1981 Apr; 1(2):121-4. PubMed ID: 6810332
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of two Hurler fetuses using an improved assay for methylumbelliferyl-alpha-L-iduronidase.
Stirling JL; Robinson D; Fensom AH; Benson PF; Baker JE; Button LR
Lancet; 1979 Jul; 2(8132):37. PubMed ID: 87908
[No Abstract] [Full Text] [Related]
8. Prenatal diagnosis of mucopolysaccharidosis I: A special difficulty arising from an unusually low enzyme activity in mother's cells.
Gatti R; Borrone C; Filocamo M; Pannone N; Di Natale P
Prenat Diagn; 1985; 5(2):149-54. PubMed ID: 3921950
[TBL] [Abstract][Full Text] [Related]
9. Comparative study of 15 lysosomal enzymes in chorionic villi and cultured amniotic fluid cells. Early prenatal diagnosis in seven pregnancies at risk for lysosomal storage diseases.
Gatti R; Lombardo C; Filocamo M; Borrone C; Porro E
Prenat Diagn; 1985; 5(5):329-36. PubMed ID: 3934658
[TBL] [Abstract][Full Text] [Related]
10. Cardiac puncture of fetus with Hurler's disease avoiding abortion of unaffected co-twin.
Aberg A; Mitelman F; Cantz M; Gehler J
Lancet; 1978 Nov; 2(8097):990-1. PubMed ID: 82009
[No Abstract] [Full Text] [Related]
11. Prenatal diagnosis of Hurler's syndrome--biochemical studies on the affected fetus.
Ikeno T; Minami R; Wagatsuma K; Fujibayashi S; Nakao T; Abo K; Tsugawa S; Taniguchi S; Takasago Y
Hum Genet; 1981; 59(4):353-9. PubMed ID: 6800929
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of the Hurler syndrome.
Pedersen C; Schwartz M; Güttler F; Hobolth N
Dan Med Bull; 1979 Nov; 26(7):357-9. PubMed ID: 160864
[No Abstract] [Full Text] [Related]
13. Antenatal diagnosis of Hurler's syndrome.
Henderson HE; Nelson MM
S Afr Med J; 1977 Feb; 51(8):241-3. PubMed ID: 403618
[TBL] [Abstract][Full Text] [Related]
14. [Use of 4-methylumbelliferryl-alpha-L-iduronide and 4-trifluoromethylumbelliferryl-alpha-L-iduronide for detecting alpha-L-iduronidase deficiencies in human tissue and for rapid prenatal diagnosis of Hurler disease].
Tsvetkova IV; Karpova EA; Voznyĭ IaV; Zolotukhina TV; Biriukov VB; Semiachkina AN
Vopr Med Khim; 1991; 37(1):74-7. PubMed ID: 1907053
[TBL] [Abstract][Full Text] [Related]
15. The Hurler syndrome: detection of patients and heterozygotes using a microassay for alpha-L-iduronidase in fibroblasts.
Kleijer WJ; Hensing-Wolffers GM; Thompson EJ; Niermeijer MF
Clin Chim Acta; 1981 Oct; 116(1):47-54. PubMed ID: 6797759
[TBL] [Abstract][Full Text] [Related]
16. Early prenatal diagnosis of Hurler's syndrome with termination of pregnancy and confirmatory findings on the fetus.
Crawfurd M; Dean MF; Hunt DM; Johnson DR; MacDonald RR; Muir H; Wright EA; Wright CR
J Med Genet; 1973 Jun; 10(2):144-53. PubMed ID: 4268390
[TBL] [Abstract][Full Text] [Related]
17. Exclusion of citrullinaemia in the first trimester of pregnancy by direct assay of argininosuccinate synthetase in chorionic villi.
Christensen E; Brandt NJ; Philip J; Bang J
Prenat Diagn; 1985; 5(4):299-301. PubMed ID: 4048069
[TBL] [Abstract][Full Text] [Related]
18. First-trimester prenatal diagnosis of aspartylglucosaminuria.
Aula P; Mattila K; Piiroinen O; Ammälä P; Von Koskull H
Prenat Diagn; 1989 Sep; 9(9):617-20. PubMed ID: 2798347
[TBL] [Abstract][Full Text] [Related]
19. Diagnosis of classical Morquio's disease: N-acetylgalactosamine 6-sulphate sulphatase activity in cultured fibroblasts, leukocytes, amniotic cells and chorionic villi.
Yuen M; Fensom AH
J Inherit Metab Dis; 1985; 8(2):80-6. PubMed ID: 3939537
[TBL] [Abstract][Full Text] [Related]
20. Immunoquantification and enzyme kinetics of alpha-L-iduronidase in cultured fibroblasts from normal controls and mucopolysaccharidosis type I patients.
Ashton LJ; Brooks DA; McCourt PA; Muller VJ; Clements PR; Hopwood JJ
Am J Hum Genet; 1992 Apr; 50(4):787-94. PubMed ID: 1550122
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
