BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

534 related articles for article (PubMed ID: 16674934)

  • 1. Lysosomal storage diseases in non-immune hydrops fetalis pregnancies.
    Kooper AJ; Janssens PM; de Groot AN; Liebrand-van Sambeek ML; van den Berg CJ; Tan-Sindhunata GB; van den Berg PP; Bijlsma EK; Smits AP; Wevers RA
    Clin Chim Acta; 2006 Sep; 371(1-2):176-82. PubMed ID: 16674934
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Hydrops fetalis as an indication for a systematic investigation into the presence of lysosomal storage diseases].
    Janssens PM; de Groot AN; de Jong JG; Liebrand-van Sambeek ML; Smits A; Wevers RA
    Ned Tijdschr Geneeskd; 2004 Feb; 148(6):264-8. PubMed ID: 15004952
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lysosomal storage diseases presenting as transient or persistent hydrops fetalis.
    Bonduelle M; Lissens W; Goossens A; De Catte L; Foulon W; Denis R; Jauniaux E; Liebaers I
    Genet Couns; 1991; 2(4):227-32. PubMed ID: 1799421
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Determination of oligosaccharides and glycolipids in amniotic fluid by electrospray ionisation tandem mass spectrometry: in utero indicators of lysosomal storage diseases.
    Ramsay SL; Maire I; Bindloss C; Fuller M; Whitfield PD; Piraud M; Hopwood JJ; Meikle PJ
    Mol Genet Metab; 2004 Nov; 83(3):231-8. PubMed ID: 15542394
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hydrops fetalis: lysosomal storage disorders in extremis.
    Stone DL; Sidransky E
    Adv Pediatr; 1999; 46():409-40. PubMed ID: 10645471
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Amniotic fluid for screening of lysosomal storage diseases presenting in utero (mainly as non-immune hydrops fetalis).
    Piraud M; Froissart R; Mandon G; Bernard A; Maire I
    Clin Chim Acta; 1996 Apr; 248(2):143-55. PubMed ID: 8740579
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Recurrent nonimmune hydrops fetalis: a rare presentation of sialic acid storage disease.
    Lefebvre G; Wehbe G; Heron D; Vautjoer Brouzes D; Choukroun JB; Darbois Y
    Genet Couns; 1999; 10(3):277-84. PubMed ID: 10546100
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fast protocol for the diagnosis of lysosomal diseases in nonimmune hydrops fetalis.
    Gort L; Granell MR; Fernández G; Carreto P; Sanchez A; Coll MJ
    Prenat Diagn; 2012 Dec; 32(12):1139-42. PubMed ID: 22991067
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Histological, biochemical, and genetic characterization of early-onset fulminating sialidosis type 2 in a Korean neonate with hydrops fetalis.
    Lee BH; Kim YM; Kim JH; Kim GH; Lee BS; Kim CJ; Yoo HJ; Yoo HW
    Brain Dev; 2014 Feb; 36(2):171-5. PubMed ID: 23433491
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inborn errors of metabolism in a cohort of pregnancies with non-immune hydrops fetalis: a single center experience.
    Bruwer Z; Al Riyami N; Al Dughaishi T; Al Murshedi F; Al Sayegh A; Al Kindy A; Meftah D; Al Kharusi K; Al Foori A; Al Yarubi N; Scott P; Al-Thihli K
    J Perinat Med; 2018 Nov; 46(9):968-974. PubMed ID: 28822227
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mucopolysaccharidosis type VII as a cause of recurrent non-immune hydrops fetalis.
    Cheng Y; Verp MS; Knutel T; Hibbard JU
    J Perinat Med; 2003; 31(6):535-7. PubMed ID: 14711113
    [TBL] [Abstract][Full Text] [Related]  

  • 12. beta-Glucuronidase deficiency as a cause of fetal hydrops.
    Kagie MJ; Kleijer WJ; Huijmans JG; Maaswinkel-Mooy P; Kanhai HH
    Am J Med Genet; 1992 Mar; 42(5):693-5. PubMed ID: 1632440
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nonimmune hydrops fetalis associated with genetic abnormalities.
    Jauniaux E; Van Maldergem L; De Munter C; Moscoso G; Gillerot Y
    Obstet Gynecol; 1990 Mar; 75(3 Pt 2):568-72. PubMed ID: 2406672
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal eradication of Hb Bart's hydrops fetalis.
    Tongsong T; Wanapirak C; Sirivatanapa P; Sa-nguansermsri T; Sirichotiyakul S; Piyamongkol W; Chanprapaph P; Steger HF; Sekararithi R; Tuggapichitti A
    J Reprod Med; 2001 Jan; 46(1):18-22. PubMed ID: 11209626
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Non-immune hydrops fetalis: A prospective study of 53 cases.
    Moreno CA; Kanazawa T; Barini R; Nomura ML; Andrade KC; Gomes CP; Heinrich JK; Giugliani R; Burin M; Cavalcanti DP
    Am J Med Genet A; 2013 Dec; 161A(12):3078-86. PubMed ID: 24039125
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of lysosomal storage diseases using fetal blood.
    Groener JE; de Graaf FL; Poorthuis BJ; Kanhai HH
    Prenat Diagn; 1999 Oct; 19(10):930-3. PubMed ID: 10521818
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Investigation of lysosomal storage diseases in nonimmune hydrops fetalis.
    Burin MG; Scholz AP; Gus R; Sanseverino MT; Fritsh A; Magalhães JA; Timm F; Barrios P; Chesky M; Coelho JC; Giugliani R
    Prenat Diagn; 2004 Aug; 24(8):653-7. PubMed ID: 15305357
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical spectrum of infantile free sialic acid storage disease.
    Lemyre E; Russo P; Melançon SB; Gagné R; Potier M; Lambert M
    Am J Med Genet; 1999 Feb; 82(5):385-91. PubMed ID: 10069709
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Diagnosis of lysosomal storage diseases with fetal presentation].
    Bouvier R; Maire I
    Ann Pathol; 1997 Sep; 17(4):277-80. PubMed ID: 9409888
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants.
    Siriratmanawong N; Pinmuang-Ngam C; Fucharoen G; Fucharoen S
    Fetal Diagn Ther; 2007; 22(4):264-8. PubMed ID: 17369692
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 27.