These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

83 related articles for article (PubMed ID: 6770331)

  • 21. 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]  

  • 22. 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]  

  • 23. Histopathological diagnosis of a type vii mucopolysaccharidosis after pregnancy termination.
    Delbecque K; Gaillez S; Schaaps JP
    Fetal Pediatr Pathol; 2009; 28(1):1-8. PubMed ID: 19116811
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Prenatal diagnosis of Maroteaux-Lamy syndrome.
    Van Dyke DL; Fluharty AL; Schafer IA; Shapiro LJ; Kihara H; Weiss L
    Am J Med Genet; 1981; 8(2):235-42. PubMed ID: 6792921
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Prenatal diagnosis of hereditary lysosomal diseases].
    Mirenburg TV; Aronovich EL; Lebedeva TV; Akhunov VS; Krasnopol'skaia KD
    Vopr Med Khim; 1988; 34(4):41-6. PubMed ID: 3143186
    [TBL] [Abstract][Full Text] [Related]  

  • 27. First experience of enzyme replacement therapy with idursulfase in Spanish patients with Hunter syndrome under 5 years of age: case observations from the Hunter Outcome Survey (HOS).
    Alcalde-Martín C; Muro-Tudelilla JM; Cancho-Candela R; Gutiérrez-Solana LG; Pintos-Morell G; Martí-Herrero M; Munguira-Aguado P; Galán-Gómez E
    Eur J Med Genet; 2010; 53(6):371-7. PubMed ID: 20709629
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal metachromatic leukodystrophy.
    Wiesmann UN; Meier C; Spycher MA; Schmid W; Bischoff A; Gautier E; Herschlowitz N
    Helv Paediatr Acta; 1975 May; 30(1):31-42. PubMed ID: 239916
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis of Hunter syndrome using fetal plasma.
    Lissens W; Van Lierde M; Decaluwe J; Foulon W; Evrard P; Van Hoof F; Freund M; Liebaers I
    Prenat Diagn; 1988 Jan; 8(1):59-62. PubMed ID: 3125535
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutations of the iduronate-2-sulfatase (IDS) gene in patients with Hunter syndrome (mucopolysaccharidosis II).
    Schröder W; Wulff K; Wehnert M; Seidlitz G; Herrmann FH
    Hum Mutat; 1994; 4(2):128-31. PubMed ID: 7981716
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Hunter syndrome: prenatal diagnosis in maternal serum.
    Zlotogora J; Bach G
    Am J Hum Genet; 1986 Feb; 38(2):253-60. PubMed ID: 3080875
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Iduronate sulfatase activity in serum, lymphocytes, and fibroblasts--simplified diagnosis of the Hunter syndrome.
    Liebaers I; Neufeld E
    Pediatr Res; 1976 Aug; 10(8):733-6. PubMed ID: 821034
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Intrauterine diagnosis of the hurler and hunter syndromes.
    Fratantoni JC; Neufeld EF; Uhlendorf BW; Jacobson CB
    N Engl J Med; 1969 Mar; 280(13):686-8. PubMed ID: 4179670
    [No Abstract]   [Full Text] [Related]  

  • 35. [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]  

  • 36. Treatment related observations in solid tissues, fibroblast cultured and amniotic fluid cells of type II glycogenosis, Hurler disease and metachromatic leukodystrophy.
    Hug G; Schubert WK; Soukup S
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):160-83. PubMed ID: 4215475
    [No Abstract]   [Full Text] [Related]  

  • 37. Iduronate sulfatase in amniotic fluid: an aid in the prenatal diagnosis of the hunter syndrome.
    Liebaers I; Di Natale P; Neufeld EF
    J Pediatr; 1977 Mar; 90(3):423-5. PubMed ID: 402458
    [No Abstract]   [Full Text] [Related]  

  • 38. Mucopolysaccharidosis type II in females: case report and review of literature.
    Tuschl K; Gal A; Paschke E; Kircher S; Bodamer OA
    Pediatr Neurol; 2005 Apr; 32(4):270-2. PubMed ID: 15797184
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Prenatal diagnosis of globoid-cell leukodystrophy (Krabbe's disease) (author's transl)].
    Harzer K; Benz HU; Knörr-Gärtner H; Jonatha WD; Knörr K
    Dtsch Med Wochenschr; 1976 May; 101(21):821-7. PubMed ID: 1269411
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Methylamine accumulation in cultured cells as a measure of the aqueous storage compartment in the laboratory diagnosis of genetic lysosomal diseases.
    Kopitz J; Harzer K; Kohlschütter A; Zöller B; Blenck N; Cantz M
    Am J Med Genet; 1996 May; 63(1):198-202. PubMed ID: 8723110
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.