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PUBMED FOR HANDHELDS

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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 10. Warfarin embryopathy in siblings.
    Harrod MJ, Sherrod PS.
    Obstet Gynecol; 1981 May 15; 57(5):673-6. PubMed ID: 7194462
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  • 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
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  • 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
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  • 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
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  • 16. Warfarin embryopathy.
    Chan KY, Gilbert-Barness E, Tiller G.
    Pediatr Pathol Mol Med; 2003 May 15; 22(4):277-83. PubMed ID: 14692224
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  • 20. Punctate epiphyses: a radiological sign not a disease.
    Poznanski AK.
    Pediatr Radiol; 1994 May 15; 24(6):418-24, 436. PubMed ID: 7700718
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