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Journal Abstract Search

129 related items for PubMed ID: 7937589

  • 1. Prenatal diagnosis of femur-fibula-ulna complex by ultrasonography in a male fetus at 24 weeks of gestation.
    Capece G, Fasolino A, Della Monica M, Lonardo F, Scarano G, Neri G.
    Prenat Diagn; 1994 Jun; 14(6):502-5. PubMed ID: 7937589
    [Abstract] [Full Text] [Related]

  • 2. [Femur-fibula-ulna (FFU) complex in the 33rd week of gestation: ultrasonography, radiology, pathology and differential diagnosis. Case report].
    Guschmann M, Becker R, Urban M, Entezami M, Hese S, Vogel M.
    Klin Padiatr; 2001 Jun; 213(5):301-5. PubMed ID: 11582532
    [Abstract] [Full Text] [Related]

  • 3. Prenatal ultrasound diagnosis of a femur-fibula-ulna complex during the first half of pregnancy.
    Florio I, Wisser J, Huch R, Huch A.
    Fetal Diagn Ther; 1999 Jun; 14(5):310-2. PubMed ID: 10529577
    [Abstract] [Full Text] [Related]

  • 4. Prenatal diagnosis of femur-fibula-ulna complex by ultrasound examination at 20 weeks of gestation.
    Geipel A, Berg C, Germer U, Krokowski M, Smrcek J, Gembruch U.
    Ultrasound Obstet Gynecol; 2003 Jul; 22(1):79-81. PubMed ID: 12858309
    [Abstract] [Full Text] [Related]

  • 5. Femur- fibula- ulna complex.
    Geniets C, Vanhoenacker F, Blaumeiser B, Parizel PM.
    JBR-BTR; 2006 Jul; 89(3):130-1. PubMed ID: 16883757
    [No Abstract] [Full Text] [Related]

  • 6. The femur, fibula, ulna (FFU) complex in siblings.
    Zlotogora J, Rosenmann E, Menashe M, Robin GC, Cohen T.
    Clin Genet; 1983 Dec; 24(6):449-52. PubMed ID: 6652959
    [Abstract] [Full Text] [Related]

  • 7. A case of femur-fibular-ulna complex with peculiar metaphyseal changes.
    Ludwig K, Tenconi R, Salmaso R.
    Fetal Pediatr Pathol; 2010 Dec; 29(4):255-60. PubMed ID: 20594150
    [Abstract] [Full Text] [Related]

  • 8. A local outbreak of femoral hypoplasia or aplasia and femoral fibula-ulnar-complex.
    Robert JM, Guibaud P, Robert E.
    J Genet Hum; 1981 Dec; 29(4):379-94. PubMed ID: 7328413
    [Abstract] [Full Text] [Related]

  • 9. FFU complex: an analysis of 491 cases.
    Lenz W, Zygulska M, Horst J.
    Hum Genet; 1993 May; 91(4):347-56. PubMed ID: 8500790
    [Abstract] [Full Text] [Related]

  • 10. Craniosynostosis with wormian bone, bowing of the long bones, unilateral short femur, and focal fibula deficiency: a prenatal diagnostic dilemma.
    Tonni G, Lituania M, Rosignoli L.
    J Clin Ultrasound; 2013 Sep; 41(7):448-52. PubMed ID: 23090838
    [Abstract] [Full Text] [Related]

  • 11. Severe hypoplasia of the right femur, ipsilateral agenesia of the fibula and twisted right foot in a 24-week-old fetus with proximal femoral focal deficiency (PFFD).
    La Torre R, Mastrone M, Coacci F, Labi L, Palma E, Di Giusto M, Patella A, Cosmi EV.
    Clin Exp Obstet Gynecol; 2003 Sep; 30(1):65-6. PubMed ID: 12731749
    [Abstract] [Full Text] [Related]

  • 12. Ultrasound-guided interscalene brachial plexus block in a child with femur fibula ulna syndrome.
    Jan van Geffen G, Tielens L, Gielen M.
    Paediatr Anaesth; 2006 Mar; 16(3):330-2. PubMed ID: 16490101
    [Abstract] [Full Text] [Related]

  • 13. Femur-fibula-ulna complex.
    Furness J, Henman P, Sturgiss S.
    Arch Dis Child Fetal Neonatal Ed; 2013 Nov; 98(6):F479. PubMed ID: 23645575
    [No Abstract] [Full Text] [Related]

  • 14. Proximal focal femoral deficiency, contralateral hip dysplasia in association with contralateral ulnar hypoplasia and clefthand: a case report and review of literatures of PFFD and/or FFU.
    Kalaycioglu A, Aynaci O.
    Okajimas Folia Anat Jpn; 2001 Aug; 78(2-3):83-9. PubMed ID: 11732209
    [Abstract] [Full Text] [Related]

  • 15. Unilateral and asymmetric limb defects in man: delineation of the femur-fibula-ulna complex.
    Lenz W, Feldmann U.
    Birth Defects Orig Artic Ser; 1977 Aug; 13(1):269-85. PubMed ID: 851600
    [No Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of Weyers syndrome (deficient ulnar and fibular rays with bilateral hydronephrosis).
    Elejalde BR, de Elejalde MM, Booth C, Kaye C, Hollison L.
    Am J Med Genet; 1985 Jul; 21(3):439-44. PubMed ID: 3895927
    [Abstract] [Full Text] [Related]

  • 17. Familial aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits in an inbred Pakistani Muslim family: a possible new autosomal recessive disorder with overlapping manifestations of the syndromes of Fuhrmann, Al-Awadi, and Raas-Rothschild.
    Kumar D, Duggan MB, Mueller RF, Karbani G.
    Am J Med Genet; 1997 May 16; 70(2):107-13. PubMed ID: 9128926
    [Abstract] [Full Text] [Related]

  • 18. Kallmann syndrome in three unrelated women and an association with femur-fibula-ulna dysostosis in one case.
    Gasztonyi Z, Barsi P, Czeizel AE.
    Am J Med Genet; 2000 Jul 31; 93(3):176-80. PubMed ID: 10925376
    [Abstract] [Full Text] [Related]

  • 19. Two sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity?
    Kardon NB, Dana LP, FitzGerald JM, Opitz JM.
    Am J Med Genet Suppl; 1986 Jul 31; 2():239-45. PubMed ID: 3146295
    [Abstract] [Full Text] [Related]

  • 20. Cross-sectional study of fetal long-bone length in an Iranian population at 17-25 weeks of gestation.
    Kasraeian M, Shahraki HR, Asadi N, Vafaei H, Sameni S.
    Int J Gynaecol Obstet; 2017 Apr 31; 137(1):20-25. PubMed ID: 28083947
    [Abstract] [Full Text] [Related]

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