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Journal Abstract Search

193 related items for PubMed ID: 10535835

  • 1. Interruption of the aortic arch at the isthmus with DiGeorge syndrome and 22q11.2 deletion.
    Takahashi K, Kuwahara T, Nagatsu M.
    Cardiol Young; 1999 Sep; 9(5):516-8. PubMed ID: 10535835
    [Abstract] [Full Text] [Related]

  • 2. 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; 9(5):463-7. PubMed ID: 10535824
    [Abstract] [Full Text] [Related]

  • 3.
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  • 4. Interrupted aortic arch type C associated with DiGeorge syndrome in 22q11.2 deletion: first case detected in Japan.
    Fujii I, Ueno Y, Kurano R, Goto Y.
    Pediatr Int; 2005 Dec; 47(6):698-700. PubMed ID: 16354229
    [No Abstract] [Full Text] [Related]

  • 5. 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 Dec; 3(1):45-8. PubMed ID: 11339377
    [Abstract] [Full Text] [Related]

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

  • 7. 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; 32(2):492-8. PubMed ID: 9708481
    [Abstract] [Full Text] [Related]

  • 8. Interrupted right aortic arch in DiGeorge syndrome.
    Moerman P, Dumoulin M, Lauweryns J, Van der Hauwaert LG.
    Br Heart J; 1987 Sep; 58(3):274-8. PubMed ID: 3663429
    [Abstract] [Full Text] [Related]

  • 9. The genetic implication for preceding generations of the prenatal diagnosis of interrupted aortic arch in association with unsuspected DiGeorge anomaly.
    Puder KS, Humes RA, Gold RL, Bawle EV, Goyert GL.
    Am J Obstet Gynecol; 1995 Jul; 173(1):239-41. PubMed ID: 7631695
    [Abstract] [Full Text] [Related]

  • 10. Ventricular septal defect and deletion of chromosome 22q11: anatomical types and aortic arch anomalies.
    Toscano A, Anaclerio S, Digilio MC, Giannotti A, Fariello G, Dallapiccola B, Marino B.
    Eur J Pediatr; 2002 Feb; 161(2):116-7. PubMed ID: 11954747
    [No Abstract] [Full Text] [Related]

  • 11. DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.
    Wilson DI, Cross IE, Goodship JA, Coulthard S, Carey AH, Scambler PJ, Bain HH, Hunter AS, Carter PE, Burn J.
    Br Heart J; 1991 Oct; 66(4):308-12. PubMed ID: 1747284
    [Abstract] [Full Text] [Related]

  • 12. Incidence and significance of 22q11.2 hemizygosity in patients with interrupted aortic arch.
    Rauch A, Hofbeck M, Leipold G, Klinge J, Trautmann U, Kirsch M, Singer H, Pfeiffer RA.
    Am J Med Genet; 1998 Jul 24; 78(4):322-31. PubMed ID: 9714433
    [Abstract] [Full Text] [Related]

  • 13. The relationship of the outlet septum to the aortic outflow tract in hearts with interruption of the aortic arch.
    al-Marsafawy HM, Ho SY, Redington AN, Anderson RH.
    J Thorac Cardiovasc Surg; 1995 Jun 24; 109(6):1225-36. PubMed ID: 7776687
    [Abstract] [Full Text] [Related]

  • 14. Isolated innominate artery in 22q11 microdeletion.
    Duke C, Chan KC.
    Pediatr Cardiol; 2001 Jun 24; 22(1):80-2. PubMed ID: 11123139
    [Abstract] [Full Text] [Related]

  • 15. Mirror-image type D interrupted aortic arch: a novel cardiac phenotype providing some perspective in the del22q11.2 syndrome.
    Lee ML, Chen M, Yang AD, Chiu IS.
    Int J Cardiol; 2010 Jun 11; 141(3):e47-50. PubMed ID: 19136166
    [Abstract] [Full Text] [Related]

  • 16. 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 11; 163(11):642-5. PubMed ID: 15300432
    [Abstract] [Full Text] [Related]

  • 17. A new embryonic linkage between chromosome 22q11 deletion and a right ductus from a right aortic arch in a neonate with DiGeorge syndrome.
    Lee ML, Chaou WT, Wang YM, Fang W, Chiu IS.
    Int J Cardiol; 2001 Jul 11; 79(2-3):315-6. PubMed ID: 11488286
    [No Abstract] [Full Text] [Related]

  • 18. 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 11; 112(6 Pt 1):e472. PubMed ID: 14654648
    [Abstract] [Full Text] [Related]

  • 19. Familial 22q11.2 deletion: an infant with interrupted aortic arch and DiGeorge syndrome delivered from by a mother with tetralogy of Fallot.
    Ito T, Okubo T, Sato H.
    Eur J Pediatr; 2002 Mar 11; 161(3):173-4. PubMed ID: 11998920
    [Abstract] [Full Text] [Related]

  • 20. Neonatal Death Caused by Interrupted Aortic Arch Associated With 22q11.2 Deletion Syndrome: An Autopsy Case Report.
    Shinkawa N, Yamaguchi M, Ozaki M, Yukawa N.
    Am J Forensic Med Pathol; 2019 Jun 11; 40(2):178-182. PubMed ID: 30562178
    [Abstract] [Full Text] [Related]

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