Jawad AF - Search Results

1

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. McElhinney DB, et al. Among authors: jawad af. Pediatrics. 2003 Dec;112(6 Pt 1):e472. doi: 10.1542/peds.112.6.e472. Pediatrics. 2003. PMID: 14654648

2

Lack of correlation between impaired T cell production, immunodeficiency, and other phenotypic features in chromosome 22q11.2 deletion syndromes.

Sullivan KE, Jawad AF, Randall P, Driscoll DA, Emanuel BS, McDonald-McGinn DM, Zackai EH. Sullivan KE, et al. Among authors: jawad af. Clin Immunol Immunopathol. 1998 Feb;86(2):141-6. doi: 10.1006/clin.1997.4463. Clin Immunol Immunopathol. 1998. PMID: 9473376 Free article.

3

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. Goldmuntz E, et al. Among authors: jawad af. J Am Coll Cardiol. 1998 Aug;32(2):492-8. doi: 10.1016/s0735-1097(98)00259-9. J Am Coll Cardiol. 1998. PMID: 9708481 Free article.

4

Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.

Gerdes M, Solot C, Wang PP, Moss E, LaRossa D, Randall P, Goldmuntz E, Clark BJ 3rd, Driscoll DA, Jawad A, Emanuel BS, McDonald-McGinn DM, Batshaw ML, Zackai EH. Gerdes M, et al. Am J Med Genet. 1999 Jul 16;85(2):127-33. Am J Med Genet. 1999. PMID: 10406665

5

Longitudinal analysis of lymphocyte function and numbers in the first year of life in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

Sullivan KE, McDonald-McGinn D, Driscoll DA, Emanuel BS, Zackai EH, Jawad AF. Sullivan KE, et al. Among authors: jawad af. Clin Diagn Lab Immunol. 1999 Nov;6(6):906-11. doi: 10.1128/CDLI.6.6.906-911.1999. Clin Diagn Lab Immunol. 1999. PMID: 10548584 Free PMC article.

6

Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

Jawad AF, McDonald-Mcginn DM, Zackai E, Sullivan KE. Jawad AF, et al. J Pediatr. 2001 Nov;139(5):715-23. doi: 10.1067/mpd.2001.118534. J Pediatr. 2001. PMID: 11713452

7

Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome.

Bearden CE, Jawad AF, Lynch DR, Sokol S, Kanes SJ, McDonald-McGinn DM, Saitta SC, Harris SE, Moss E, Wang PP, Zackai E, Emanuel BS, Simon TJ. Bearden CE, et al. Among authors: jawad af. Am J Psychiatry. 2004 Sep;161(9):1700-2. doi: 10.1176/appi.ajp.161.9.1700. Am J Psychiatry. 2004. PMID: 15337663

8

The 22q11.2 deletion in African-American patients: an underdiagnosed population?

McDonald-McGinn DM, Minugh-Purvis N, Kirschner RE, Jawad A, Tonnesen MK, Catanzaro JR, Goldmuntz E, Driscoll D, Larossa D, Emanuel BS, Zackai EH. McDonald-McGinn DM, et al. Am J Med Genet A. 2005 Apr 30;134(3):242-6. doi: 10.1002/ajmg.a.30069. Am J Med Genet A. 2005. PMID: 15754359 Free PMC article.

9

Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome.

Bearden CE, Jawad AF, Lynch DR, Monterossso JR, Sokol S, McDonald-McGinn DM, Saitta SC, Harris SE, Moss E, Wang PP, Zackai E, Emanuel BS, Simon TJ. Bearden CE, et al. Among authors: jawad af. Child Neuropsychol. 2005 Feb;11(1):109-17. doi: 10.1080/09297040590911239. Child Neuropsychol. 2005. PMID: 15846854 Free PMC article.

10

Neo-aortic valvar function after the arterial switch.

Marino BS, Wernovsky G, McElhinney DB, Jawad A, Kreb DL, Mantel SF, van der Woerd WL, Robbers-Visser D, Novello R, Gaynor JW, Spray TL, Cohen MS. Marino BS, et al. Cardiol Young. 2006 Oct;16(5):481-9. doi: 10.1017/S1047951106000953. Cardiol Young. 2006. PMID: 16984700

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