Sullivan K - Search Results

1

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. Among authors: sullivan k. Genet Couns. 1999;10(1):11-24. Genet Couns. 1999. PMID: 10191425

2

Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.

McDonald-McGinn DM, Driscoll DA, Bason L, Christensen K, Lynch D, Sullivan K, Canning D, Zavod W, Quinn N, Rome J. McDonald-McGinn DM, et al. Among authors: sullivan k. Am J Med Genet. 1995 Oct 23;59(1):103-13. doi: 10.1002/ajmg.1320590122. Am J Med Genet. 1995. PMID: 8849001

3

Juvenile rheumatoid arthritis-like polyarthritis in chromosome 22q11.2 deletion syndrome (DiGeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome).

Sullivan KE, McDonald-McGinn DM, Driscoll DA, Zmijewski CM, Ellabban AS, Reed L, Emanuel BS, Zackai EH, Athreya BH, Keenan G. Sullivan KE, et al. Arthritis Rheum. 1997 Mar;40(3):430-6. doi: 10.1002/art.1780400307. Arthritis Rheum. 1997. PMID: 9082929

4

Arthritis associated with deletion of 22q11.2: more common than previously suspected.

Keenan GF, Sullivan KE, McDonald-McGinn DM, Zackai EH. Keenan GF, et al. Among authors: sullivan ke. Am J Med Genet. 1997 Sep 5;71(4):488. Am J Med Genet. 1997. PMID: 9286462 No abstract available.

5

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.

6

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. Among authors: sullivan ke. 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.

7

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. Among authors: sullivan k. Genet Test. 1997;1(2):99-108. doi: 10.1089/gte.1997.1.99. Genet Test. 1997. PMID: 10464633

8

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.

9

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. Among authors: sullivan ke. J Pediatr. 2001 Nov;139(5):715-23. doi: 10.1067/mpd.2001.118534. J Pediatr. 2001. PMID: 11713452

10

Graves' disease in patients with 22q11.2 deletion.

Kawame H, Adachi M, Tachibana K, Kurosawa K, Ito F, Gleason MM, Weinzimer S, Levitt-Katz L, Sullivan K, McDonald-McGinn DM. Kawame H, et al. Among authors: sullivan k. J Pediatr. 2001 Dec;139(6):892-5. doi: 10.1067/mpd.2001.119448. J Pediatr. 2001. PMID: 11743521

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