McDonald-McGinn D - Search Results

1

Diagnosis of 22q11.2 deletion syndrome and artemis deficiency in two children with T-B-NK+ immunodeficiency.

Heimall J, Keller M, Saltzman R, Bunin N, McDonald-McGinn D, Zakai E, de Villartay JP, Moshous D, Ariue B, McCarthy EA, Devlin BH, Parikh S, Buckley RH, Markert ML. Heimall J, et al. J Clin Immunol. 2012 Oct;32(5):1141-4. doi: 10.1007/s10875-012-9741-9. Epub 2012 Aug 3. J Clin Immunol. 2012. PMID: 22864628

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. Clin Immunol Immunopathol. 1998 Feb;86(2):141-6. doi: 10.1006/clin.1997.4463. Clin Immunol Immunopathol. 1998. PMID: 9473376 Free article.

3

Increased prevalence of immunoglobulin A deficiency in patients with the chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

Smith CA, Driscoll DA, Emanuel BS, McDonald-McGinn DM, Zackai EH, Sullivan KE. Smith CA, et al. Clin Diagn Lab Immunol. 1998 May;5(3):415-7. doi: 10.1128/CDLI.5.3.415-417.1998. Clin Diagn Lab Immunol. 1998. PMID: 9606003 Free PMC article.

4

The Philadelphia story: the 22q11.2 deletion: report on 250 patients.

McDonald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Solot C, Wang P, Jacobs I, Handler S, Knightly C, Heher K, Wilson M, Ming JE, Grace K, Driscoll D, Pasquariello P, Randall P, Larossa D, Emanuel BS, Zackai EH. McDonald-McGinn DM, et al. Genet Couns. 1999;10(1):11-24. Genet Couns. 1999. PMID: 10191425

5

The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients.

McDonald-McGinn DM, LaRossa D, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Wang P, Solot C, Schultz P, Lynch D, Bingham P, Keenan G, Weinzimer S, Ming JE, Driscoll D, Clark BJ 3rd, Markowitz R, Cohen A, Moshang T, Pasquariello P, Randall P, Emanuel BS, Zackai EH. McDonald-McGinn DM, et al. Genet Test. 1997;1(2):99-108. doi: 10.1089/gte.1997.1.99. Genet Test. 1997. PMID: 10464633

6

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. 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.

7

The 22q11.2 deletion syndrome.

Emanuel BS, McDonald-McGinn D, Saitta SC, Zackai EH. Emanuel BS, et al. Adv Pediatr. 2001;48:39-73. Adv Pediatr. 2001. PMID: 11480765 Review.

8

Safety of live viral vaccines in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

Perez EE, Bokszczanin A, McDonald-McGinn D, Zackai EH, Sullivan KE. Perez EE, et al. Pediatrics. 2003 Oct;112(4):e325. doi: 10.1542/peds.112.4.e325. Pediatrics. 2003. PMID: 14523220

9

Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.

Staple L, Andrews T, McDonald-McGinn D, Zackai E, Sullivan KE. Staple L, et al. Pediatr Allergy Immunol. 2005 May;16(3):226-30. doi: 10.1111/j.1399-3038.2005.00259.x. Pediatr Allergy Immunol. 2005. PMID: 15853951

10

Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome.

Goldmuntz E, Driscoll DA, Emanuel BS, McDonald-McGinn D, Mei M, Zackai E, Mitchell LE. Goldmuntz E, et al. Birth Defects Res A Clin Mol Teratol. 2009 Feb;85(2):125-9. doi: 10.1002/bdra.20501. Birth Defects Res A Clin Mol Teratol. 2009. PMID: 18770859 Free PMC article.

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