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Journal Abstract Search
219 related items for PubMed ID: 17676222
1. Second-trimester diagnosis of osteogenesis imperfecta associated with schizencephaly by sonography. Ozkur A, Kervancioglu R, Kervancioglu S, Dikensoy E, Bayram M. Saudi Med J; 2007 Aug; 28(8):1289-90. PubMed ID: 17676222 [Abstract] [Full Text] [Related]
2. A case of fetal osteogenesis imperfecta type 2A: longitudinal observation of natural course in utero and pitfalls for prenatal ultrasound diagnosis. Kimura I, Araki R, Yoshizato T, Miyamoto S. J Med Ultrason (2001); 2015 Oct; 42(4):565-70. PubMed ID: 26576983 [Abstract] [Full Text] [Related]
6. Anencephaly in a fetus with osteogenesis imperfecta: early diagnosis by transvaginal sonography. Bronshtein M, Weiner Z. Prenat Diagn; 1992 Oct; 12(10):831-4. PubMed ID: 1475252 [Abstract] [Full Text] [Related]
7. [Prenatal diagnosis of osteogenesis imperfecta. Report of a case]. Giancotti A, Cioni M, Careri I, Longo G, Lucantoni V, Pachì A. Minerva Ginecol; 1999 Dec; 51(12):505-8. PubMed ID: 10767999 [Abstract] [Full Text] [Related]
8. Management of osteogenesis imperfecta in pregnancy. A case report. Carlson JW, Harlass FE. J Reprod Med; 1993 Mar; 38(3):228-32. PubMed ID: 8487243 [Abstract] [Full Text] [Related]
11. [Update on prenatal diagnosis of osteogenesis imperfecta type II : an index case report diagnosed by ultrasonography in the first trimester]. Buisson O, Senat MV, Laurenceau N, Ville Y. J Gynecol Obstet Biol Reprod (Paris); 2002 Nov; 31(7):672-6. PubMed ID: 12457140 [Abstract] [Full Text] [Related]
13. [Prenatal diagnosis of osteogenesis imperfecta. Report of a case classified as the classical Ekman Lobstein type]. Chalubinski K, Schaller A. Ultraschall Med; 1994 Feb; 15(1):38-42. PubMed ID: 8165462 [Abstract] [Full Text] [Related]
14. First-trimester diagnosis of osteogenesis imperfecta associated with encephalocele by conventional and three-dimensional ultrasound. Ruano R, Picone O, Benachi A, Grebille AG, Martinovic J, Dumez Y, Dommergues M. Prenat Diagn; 2003 Jul; 23(7):539-42. PubMed ID: 12868078 [Abstract] [Full Text] [Related]
15. Osteogenesis imperfecta type I: second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the paucisymptomatic father. Chen CP, Su YN, Chang TY, Chern SR, Chen CY, Su JW, Wang W. Taiwan J Obstet Gynecol; 2012 Jun; 51(2):276-9. PubMed ID: 22795108 [Abstract] [Full Text] [Related]