These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

348 related items for PubMed ID: 11419896

  • 1. Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching.
    McElhinney DB, Clark BJ, Weinberg PM, Kenton ML, McDonald-McGinn D, Driscoll DA, Zackai EH, Goldmuntz E.
    J Am Coll Cardiol; 2001 Jun 15; 37(8):2114-9. PubMed ID: 11419896
    [Abstract] [Full Text] [Related]

  • 2. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion.
    Momma K, Kondo C, Matsuoka R.
    J Am Coll Cardiol; 1996 Jan 15; 27(1):198-202. PubMed ID: 8522695
    [Abstract] [Full Text] [Related]

  • 3. Laterality of the aortic arch and anomalies of the subclavian artery-reliable indicators for 22q11.2 deletion syndromes?
    Rauch R, Rauch A, Koch A, Zink S, Kaulitz R, Girisch M, Singer H, Hofbeck M.
    Eur J Pediatr; 2004 Nov 15; 163(11):642-5. PubMed ID: 15300432
    [Abstract] [Full Text] [Related]

  • 4. Cardiovascular anomalies in patients diagnosed with a chromosome 22q11 deletion beyond 6 months of age.
    McElhinney DB, McDonald-McGinn D, Zackai EH, Goldmuntz E.
    Pediatrics; 2001 Dec 15; 108(6):E104. PubMed ID: 11731631
    [Abstract] [Full Text] [Related]

  • 5. Aortic arch anomalies associated with chromosome 22q11 deletion (CATCH 22).
    Momma K, Matsuoka R, Takao A.
    Pediatr Cardiol; 1999 Dec 15; 20(2):97-102. PubMed ID: 9986884
    [Abstract] [Full Text] [Related]

  • 6. Frequency of 22q11 deletions in patients with conotruncal defects.
    Goldmuntz E, Clark BJ, Mitchell LE, Jawad AF, Cuneo BF, Reed L, McDonald-McGinn D, Chien P, Feuer J, Zackai EH, Emanuel BS, Driscoll DA.
    J Am Coll Cardiol; 1998 Aug 15; 32(2):492-8. PubMed ID: 9708481
    [Abstract] [Full Text] [Related]

  • 7. Chromosome 22q11 deletion in patients with ventricular septal defect: frequency and associated cardiovascular anomalies.
    McElhinney DB, Driscoll DA, Levin ER, Jawad AF, Emanuel BS, Goldmuntz E.
    Pediatrics; 2003 Dec 15; 112(6 Pt 1):e472. PubMed ID: 14654648
    [Abstract] [Full Text] [Related]

  • 8. Aortic arch anomalies detected in foetal life by echocardiography.
    Oztunc F, Ugan Atik S, Dedeoglu R, Yuksel MA, Madazlı R.
    J Obstet Gynaecol; 2018 Jul 15; 38(5):647-651. PubMed ID: 29430994
    [Abstract] [Full Text] [Related]

  • 9. Patterns of right aortic arch and mirror-image branching of the brachiocephalic vessels without associated anomalies.
    McElhinney DB, Hoydu AK, Gaynor JW, Spray TL, Goldmuntz E, Weinberg PM.
    Pediatr Cardiol; 2001 Jul 15; 22(4):285-91. PubMed ID: 11455394
    [Abstract] [Full Text] [Related]

  • 10. Anatomic patterns of conotruncal defects associated with deletion 22q11.
    Marino B, Digilio MC, Toscano A, Anaclerio S, Giannotti A, Feltri C, de Ioris MA, Angioni A, Dallapiccola B.
    Genet Med; 2001 Jul 15; 3(1):45-8. PubMed ID: 11339377
    [Abstract] [Full Text] [Related]

  • 11. Chromosome 22q11 deletion in patients with truncus arteriosus.
    McElhinney DB, Driscoll DA, Emanuel BS, Goldmuntz E.
    Pediatr Cardiol; 2003 Jul 15; 24(6):569-73. PubMed ID: 12947506
    [Abstract] [Full Text] [Related]

  • 12. Persistent fifth aortic arch associated with 22q11.2 deletion syndrome.
    Lee ML, Chen HN, Chen M, Tsao LY, Wang BT, Lee MH, Chiu IS.
    J Formos Med Assoc; 2006 Apr 15; 105(4):284-9. PubMed ID: 16618608
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome.
    Momma K.
    Am J Cardiol; 2010 Jun 01; 105(11):1617-24. PubMed ID: 20494672
    [Abstract] [Full Text] [Related]

  • 15. Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery.
    Ziolkowska L, Kawalec W, Turska-Kmiec A, Krajewska-Walasek M, Brzezinska-Rajszys G, Daszkowska J, Maruszewski B, Burczynski P.
    Eur J Pediatr; 2008 Oct 01; 167(10):1135-40. PubMed ID: 18172682
    [Abstract] [Full Text] [Related]

  • 16. [Double aortic arch: prenatal case report].
    Budziszewska P, Kuka D, Sodowski M, Sodowski K, Jeanty P, Skrzypulec V.
    Ginekol Pol; 2009 Sep 01; 80(9):712-5. PubMed ID: 19886248
    [Abstract] [Full Text] [Related]

  • 17. Interruption of the aortic arch associated with deletion of chromosome 22q11 is associated with a subarterial and doubly committed ventricular septal defect in Japanese patients.
    Momma K, Ando M, Matsuoka R, Joo K.
    Cardiol Young; 1999 Sep 01; 9(5):463-7. PubMed ID: 10535824
    [Abstract] [Full Text] [Related]

  • 18. Cardiovascular anomalies in patients with chromosome 22q11.2 deletion: a Korean multicenter study.
    Park IS, Ko JK, Kim YH, Yoo HW, Seo EJ, Choi JY, Gil HY, Kim SJ.
    Int J Cardiol; 2007 Jan 08; 114(2):230-5. PubMed ID: 16824627
    [Abstract] [Full Text] [Related]

  • 19. [Prenatally detected aortic arch anomalies and their consequences after birth].
    Tidrenczel Z, P Tardy E, Ladányi A, Hajdú J, Böjtös I, Sarkadi E, Simon J, Demeter J.
    Orv Hetil; 2023 Jul 16; 164(28):1111-1120. PubMed ID: 37454329
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 18.