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144 related items for PubMed ID: 20594150
1. A case of femur-fibular-ulna complex with peculiar metaphyseal changes. Ludwig K, Tenconi R, Salmaso R. Fetal Pediatr Pathol; 2010; 29(4):255-60. PubMed ID: 20594150 [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; 213(5):301-5. PubMed ID: 11582532 [Abstract] [Full Text] [Related]
3. 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]
4. 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]
5. 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 01; 13(1):269-85. PubMed ID: 851600 [No Abstract] [Full Text] [Related]
6. 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]
7. FFU complex: an analysis of 491 cases. Lenz W, Zygulska M, Horst J. Hum Genet; 1993 May 01; 91(4):347-56. PubMed ID: 8500790 [Abstract] [Full Text] [Related]
8. 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]
9. 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 Jun 01; 48(4):380-2. PubMed ID: 17290579 [Abstract] [Full Text] [Related]
11. 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 01; 22(1):79-81. PubMed ID: 12858309 [Abstract] [Full Text] [Related]
12. Absence of fibula and ulna with oligodactyly, contractures, right-angle bowing of femora, abnormal facial morphology, cleft lip/palate and brain malformation in two sibs: a possibly new lethal syndrome. Pfeiffer RA, Stöss H, Voight HJ, Wündisch GF. Am J Med Genet; 1988 Apr 01; 29(4):901-8. PubMed ID: 3400735 [Abstract] [Full Text] [Related]
14. Proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H): a model of a developmental field defect. Sorge G, Ardito S, Genuardi M, Pavone V, Rizzo R, Conti G, Neri G, Katz BE, Opitz JM. Am J Med Genet; 1995 Feb 13; 55(4):427-32. PubMed ID: 7762582 [Abstract] [Full Text] [Related]
15. 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 13; 78(2-3):83-9. PubMed ID: 11732209 [Abstract] [Full Text] [Related]
16. Fibular aplasia with ectrodactyly--broadening the clinical spectrum. Gieruszczak-Bialek D, Oldak M, Skorka A, Waligora J, Korniszewski L. Eur J Med Genet; 2006 Aug 13; 49(1):83-6. PubMed ID: 16473314 [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. A local outbreak of femoral hypoplasia or aplasia and femoral fibula-ulnar-complex. Robert JM, Guibaud P, Robert E. J Genet Hum; 1981 Dec 16; 29(4):379-94. PubMed ID: 7328413 [Abstract] [Full Text] [Related]
19. Dysmelia. A classification and a pattern of malformation in a group of congenital defects of the limbs. Henkel L, Willert HG. J Bone Joint Surg Br; 1969 Aug 16; 51(3):399-414. PubMed ID: 5820783 [No Abstract] [Full Text] [Related]
20. Two rare developmental defects of the lower limbs with confirmation of the Lewin and Opitz hypothesis on the fibular and tibial developmental fields. Pavone L, Viljoen D, Ardito S, Rizzo R, Neri G, Longo G, Beighton P. Am J Med Genet; 1989 Jun 16; 33(2):161-4. PubMed ID: 2764023 [Abstract] [Full Text] [Related] Page: [Next] [New Search]