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Journal Abstract Search

135 related items for PubMed ID: 8500790

  • 1. 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]

  • 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 May; 213(5):301-5. PubMed ID: 11582532
    [Abstract] [Full Text] [Related]

  • 3. 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 May; 2():239-45. PubMed ID: 3146295
    [Abstract] [Full Text] [Related]

  • 4. [Defects of the femur and fibula with amelia, peromelia or ulnar defects of the arm. A syndrome].
    Kühne D, Lenz W, Petersen D, Schönenberg H.
    Humangenetik; 1967 May; 3(3):244-63. PubMed ID: 6074386
    [No Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. 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]

  • 7. Humeroradial synostosis, ulnar aplasia and oligodactyly, with contralateral amelia, in a child with prenatal cocaine exposure.
    Marles SL, Reed M, Evans JA.
    Am J Med Genet A; 2003 Jan 01; 116A(1):85-9. PubMed ID: 12476458
    [Abstract] [Full Text] [Related]

  • 8. 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 01; 78(2-3):83-9. PubMed ID: 11732209
    [Abstract] [Full Text] [Related]

  • 9. A local outbreak of femoral hypoplasia or aplasia and femoral fibula-ulnar-complex.
    Robert JM, Guibaud P, Robert E.
    J Genet Hum; 1981 Dec 01; 29(4):379-94. PubMed ID: 7328413
    [Abstract] [Full Text] [Related]

  • 10. 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 01; 14(6):502-5. PubMed ID: 7937589
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 14(5):310-2. PubMed ID: 10529577
    [Abstract] [Full Text] [Related]

  • 12. [Thalidomide (Contergan) induced limb deficiency in Hungary?].
    Gidai J, Bács E, Czeizel E.
    Orv Hetil; 2009 Jun 21; 150(25):1179-81. PubMed ID: 19497840
    [Abstract] [Full Text] [Related]

  • 13. Unilateral and asymmetric limb defects in man: delineation of the femur-fibula-ulna complex.
    Lenz W, Feldmann U.
    Birth Defects Orig Artic Ser; 1977 Jun 21; 13(1):269-85. PubMed ID: 851600
    [No Abstract] [Full Text] [Related]

  • 14. 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 21; 22(1):79-81. PubMed ID: 12858309
    [Abstract] [Full Text] [Related]

  • 15. Causal study of isolated ulnar-fibular deficiency in Hungary, 1975-1984.
    Czeizel AE, Vitéz M, Kodaj I, Lenz W.
    Am J Med Genet; 1993 Jun 01; 46(4):427-33. PubMed ID: 8357016
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 16(3):330-2. PubMed ID: 16490101
    [Abstract] [Full Text] [Related]

  • 17. Hemimelia in Brachmann-de Lange syndrome (BDLS): a patient with severe deficiency of the upper and lower limbs.
    Pfeiffer RA, Correll J.
    Am J Med Genet; 1993 Nov 15; 47(7):1014-7. PubMed ID: 8291514
    [Abstract] [Full Text] [Related]

  • 18. A case with proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H) associated with urogenital anomalies.
    Ergin H, Semerci CN, Bican M, Düzcan F, Yagci AB, Erdogan KM, Tufan AC.
    Turk J Pediatr; 2006 Nov 15; 48(4):380-2. PubMed ID: 17290579
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Familial occurrence of bifid femur and monodactylous ectrodactyly.
    Gollop TR, Lucchesi E, Martins RM, Nione AS.
    Am J Med Genet; 1980 Jul 31; 7(3):319-22. PubMed ID: 7468656
    [Abstract] [Full Text] [Related]

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