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Journal Abstract Search
231 related items for PubMed ID: 9382132
1. Vitamin K deficiency embryopathy: a phenocopy of the warfarin embryopathy due to a disorder of embryonic vitamin K metabolism. Menger H, Lin AE, Toriello HV, Bernert G, Spranger JW. Am J Med Genet; 1997 Oct 17; 72(2):129-34. PubMed ID: 9382132 [Abstract] [Full Text] [Related]
2. Chondrodysplasia Punctata: A Case Report of Fetal Warfarin Syndrome. Songmen S, Panta OB, Paudel SS, Ghimire RK. J Nepal Health Res Counc; 2017 Jan 17; 15(1):81-84. PubMed ID: 28714498 [Abstract] [Full Text] [Related]
3. [Warfarin fetopathy]. Bony C, Zyka F, Tiran-Rajaofera I, Attali T, De Napoli S, Alessandri JL. Arch Pediatr; 2002 Jul 17; 9(7):705-8. PubMed ID: 12162160 [Abstract] [Full Text] [Related]
4. Cervical spine abnormalities and instability with myelopathy in warfarin-related chondrodysplasia: 17-year follow-up. Takano H, Smith WL, Sato Y, Kao SC. Pediatr Radiol; 1998 Jul 17; 28(7):497-9. PubMed ID: 9662566 [Abstract] [Full Text] [Related]
5. Chondrodysplasia punctata associated with malabsorption from bariatric procedures. Kang L, Marty D, Pauli RM, Mendelsohn NJ, Prachand V, Waggoner D. Surg Obes Relat Dis; 2010 Jul 17; 6(1):99-101. PubMed ID: 19640801 [No Abstract] [Full Text] [Related]
6. Cervical spine stenosis and possible vitamin K deficiency embryopathy in an unusual case of chondrodysplasia punctata and an updated classification system. Eash DD, Weaver DD, Brunetti-Pierri N. Am J Med Genet A; 2003 Sep 15; 122A(1):70-5. PubMed ID: 12949976 [Abstract] [Full Text] [Related]
7. Phenocopy of warfarin syndrome in an infant born to a mother with sickle cell anemia and severe transfusional iron overload. Xie Y, Pivnick EK, Cohen HL, Adams-Graves PE, Pourcyrous M, Aygun B, Hankins JS. J Pediatr Hematol Oncol; 2013 Aug 15; 35(6):e265-8. PubMed ID: 23018567 [Abstract] [Full Text] [Related]
10. Warfarin embryopathy in siblings. Harrod MJ, Sherrod PS. Obstet Gynecol; 1981 May 15; 57(5):673-6. PubMed ID: 7194462 [Abstract] [Full Text] [Related]
11. Maternal vitamin K deficient embryopathy: association with hyperemesis gravidarum and Crohn disease. Toriello HV, Erick M, Alessandri JL, Bailey D, Brunetti-Pierri N, Cox H, Fryer A, Marty D, McCurdy C, Mulliken JB, Murphy H, Omlor J, Pauli RM, Ranells JD, Sanchez-Valle A, Tobiasz A, Van Maldergem L, Lin AE. Am J Med Genet A; 2013 Mar 15; 161A(3):417-29. PubMed ID: 23404932 [Abstract] [Full Text] [Related]
14. Fetotoxicity of warfarin anticoagulation. Mehndiratta S, Suneja A, Gupta B, Bhatt S. Arch Gynecol Obstet; 2010 Sep 15; 282(3):335-7. PubMed ID: 20111969 [Abstract] [Full Text] [Related]
15. Common phenotype and etiology in warfarin embryopathy and X-linked chondrodysplasia punctata (CDPX). Savarirayan R. Pediatr Radiol; 1999 May 15; 29(5):322. PubMed ID: 10382206 [No Abstract] [Full Text] [Related]
16. Warfarin embryopathy. Chan KY, Gilbert-Barness E, Tiller G. Pediatr Pathol Mol Med; 2003 May 15; 22(4):277-83. PubMed ID: 14692224 [Abstract] [Full Text] [Related]