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Journal Abstract Search

161 related items for PubMed ID: 15966048

  • 1. Prenatal magnetic resonance imaging of Galloway-Mowat syndrome.
    Chen CP, Chang TY, Lin SP, Huang JK, Tsai JD, Chiu NC, Wang W.
    Prenat Diagn; 2005 Jun; 25(6):525-7. PubMed ID: 15966048
    [No Abstract] [Full Text] [Related]

  • 2. Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findings.
    Chen CP, Lin SP, Liu YP, Tsai JD, Chen CY, Shih SL, Tsai FJ, Wu PC, Wang W.
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):212-6. PubMed ID: 21791310
    [Abstract] [Full Text] [Related]

  • 3. Perinatal imaging findings of Galloway-Mowat syndrome.
    Chen CP, Lin SP, Tsai JD, Huang JK, Yen JL, Tseng CC, Wang W.
    Genet Couns; 2007 Jun; 18(3):353-5. PubMed ID: 18019379
    [No Abstract] [Full Text] [Related]

  • 4. [Primordial growth deficiency--a case report for the diagnosis of early intrauterine growth retardation].
    Klug PW, Krainer F.
    Z Geburtshilfe Perinatol; 1986 Jun; 190(3):137-9. PubMed ID: 3532596
    [Abstract] [Full Text] [Related]

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  • 6. Late-onset growth restriction in Galloway-Mowat syndrome: a case report.
    Kang L, Kuo PL, Lee KH, Liu YC, Chang CH, Chang FM, Lin SJ.
    Prenat Diagn; 2005 Feb; 25(2):159-62. PubMed ID: 15712336
    [Abstract] [Full Text] [Related]

  • 7.
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  • 8. Early prenatal diagnosis of cloacal exstrophy with fetal magnetic resonance imaging.
    Gobbi D, Fascetti Leon F, Tregnaghi A, Gamba PG, Midrio P.
    Fetal Diagn Ther; 2008 Feb; 24(4):437-9. PubMed ID: 19023209
    [Abstract] [Full Text] [Related]

  • 9. Galloway-Mowat syndrome.
    Akhtar N, Kiran S, Hafeez F.
    J Coll Physicians Surg Pak; 2008 Aug; 18(8):520-1. PubMed ID: 18798594
    [Abstract] [Full Text] [Related]

  • 10. Fetal hemophagocytic lymphohistiocytosis in a premature infant.
    Nitta A, Suzumura H, Watabe Y, Okuya M, Nakajima D, Kurosawa H, Sugita K, Arisaka O.
    J Pediatr; 2007 Jul; 151(1):98. PubMed ID: 17586201
    [No Abstract] [Full Text] [Related]

  • 11. The association between oligohydramnios and intrauterine growth retardation.
    Lin CC, Sheikh Z, Lopata R.
    Obstet Gynecol; 1990 Dec; 76(6):1100-4. PubMed ID: 2234721
    [Abstract] [Full Text] [Related]

  • 12. [The value of the symphysis-fundus measurement in prenatal care].
    Feiks A, Gring H, Gruber W.
    Gynakol Rundsch; 1988 Dec; 28 Suppl 2():135-7. PubMed ID: 3234902
    [No Abstract] [Full Text] [Related]

  • 13. [Ultrasonic studies in fetal growth retardation].
    Ruseva R, Marinov B.
    Akush Ginekol (Sofiia); 1985 Dec; 24(4):76-82. PubMed ID: 3904500
    [No Abstract] [Full Text] [Related]

  • 14. Correlation of measured amnionic fluid volume to sonographic and magnetic resonance predictions.
    Zaretsky MV, McIntire DD, Reichel TF, Twickler DM.
    Am J Obstet Gynecol; 2004 Dec; 191(6):2148-53. PubMed ID: 15592305
    [Abstract] [Full Text] [Related]

  • 15. [Fetal behavior and motor activity].
    Gnirs J, Schneider KT.
    Gynakologe; 1994 Jun; 27(3):136-45. PubMed ID: 7926956
    [No Abstract] [Full Text] [Related]

  • 16. Evaluation of antepartum fetal well-being by measuring growth.
    Tropper PJ, Fox HE.
    Clin Perinatol; 1982 Jun; 9(2):271-84. PubMed ID: 6749371
    [No Abstract] [Full Text] [Related]

  • 17. Detection of fetal lactate with two-dimensional-localized proton magnetic resonance spectroscopy.
    Robinson JN, Cleary-Goldman J, Arias-Mendoza F, Cruz-Lobo J, Tempany C, Mulkern RV, Feinberg BB, Brown TR.
    Obstet Gynecol; 2004 Nov; 104(5 Pt 2):1208-10. PubMed ID: 15516455
    [Abstract] [Full Text] [Related]

  • 18. Fowler-like syndrome with extreme oligohydramnios, growth restriction and without muscular hypoplasia.
    Halder A, Panigrahi I, Pal L.
    Indian Pediatr; 2003 May; 40(5):418-23. PubMed ID: 12768045
    [Abstract] [Full Text] [Related]

  • 19. Late-onset nephrotic syndrome and severe cerebellar atrophy in Galloway-Mowat syndrome.
    Steiss JO, Gross S, Neubauer BA, Hahn A.
    Neuropediatrics; 2005 Oct; 36(5):332-5. PubMed ID: 16217710
    [Abstract] [Full Text] [Related]

  • 20. Prenatal genetic diagnosis of Neu-Laxova syndrome.
    Wood AM, Mottola AT, Rhee EH, Kuller JA.
    J Obstet Gynaecol; 2018 Apr; 38(3):413-414. PubMed ID: 28903583
    [No Abstract] [Full Text] [Related]

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