Gaspar HB - Search Results

1

Autologous Ex Vivo Lentiviral Gene Therapy for Adenosine Deaminase Deficiency.

Kohn DB, Booth C, Shaw KL, Xu-Bayford J, Garabedian E, Trevisan V, Carbonaro-Sarracino DA, Soni K, Terrazas D, Snell K, Ikeda A, Leon-Rico D, Moore TB, Buckland KF, Shah AJ, Gilmour KC, De Oliveira S, Rivat C, Crooks GM, Izotova N, Tse J, Adams S, Shupien S, Ricketts H, Davila A, Uzowuru C, Icreverzi A, Barman P, Campo Fernandez B, Hollis RP, Coronel M, Yu A, Chun KM, Casas CE, Zhang R, Arduini S, Lynn F, Kudari M, Spezzi A, Zahn M, Heimke R, Labik I, Parrott R, Buckley RH, Reeves L, Cornetta K, Sokolic R, Hershfield M, Schmidt M, Candotti F, Malech HL, Thrasher AJ, Gaspar HB. Kohn DB, et al. Among authors: gaspar hb. N Engl J Med. 2021 May 27;384(21):2002-2013. doi: 10.1056/NEJMoa2027675. Epub 2021 May 11. N Engl J Med. 2021. PMID: 33974366 Free PMC article. Clinical Trial.

2

Intrinsic defects of B cell function in X-linked severe combined immunodeficiency.

White H, Thrasher A, Veys P, Kinnon C, Gaspar HB. White H, et al. Among authors: gaspar hb. Eur J Immunol. 2000 Mar;30(3):732-7. doi: 10.1002/1521-4141(200003)30:3<732::AID-IMMU732>3.0.CO;2-L. Eur J Immunol. 2000. PMID: 10741387 Free article.

3

Diagnosis of X-linked lymphoproliferative disease by analysis of SLAM-associated protein expression.

Gilmour KC, Cranston T, Jones A, Davies EG, Goldblatt D, Thrasher A, Kinnon C, Nichols KE, Gaspar HB. Gilmour KC, et al. Among authors: gaspar hb. Eur J Immunol. 2000 Jun;30(6):1691-7. doi: 10.1002/1521-4141(200006)30:6<1691::AID-IMMU1691>3.0.CO;2-K. Eur J Immunol. 2000. PMID: 10898506 Free article.

4

Severe combined immunodeficiency--molecular pathogenesis and diagnosis.

Gaspar HB, Gilmour KC, Jones AM. Gaspar HB, et al. Arch Dis Child. 2001 Feb;84(2):169-73. doi: 10.1136/adc.84.2.169. Arch Dis Child. 2001. PMID: 11159300 Free PMC article. Review. No abstract available.

5

Protein assays for diagnosis of Wiskott-Aldrich syndrome and X-linked thrombocytopenia.

Qasim W, Gilmour KC, Heath S, Ashton E, Cranston T, Thomas A, Finn A, Davies EG, Thrasher AJ, Kinnon C, Jones A, Gaspar HB. Qasim W, et al. Among authors: gaspar hb. Br J Haematol. 2001 Jun;113(4):861-5. doi: 10.1046/j.1365-2141.2001.02832.x. Br J Haematol. 2001. PMID: 11442475 Free article.

6

Cognitive and behavioral abnormalities in adenosine deaminase deficient severe combined immunodeficiency.

Rogers MH, Lwin R, Fairbanks L, Gerritsen B, Gaspar HB. Rogers MH, et al. Among authors: gaspar hb. J Pediatr. 2001 Jul;139(1):44-50. doi: 10.1067/mpd.2001.115023. J Pediatr. 2001. PMID: 11445793

7

Defective expression of the interleukin-2/interleukin-15 receptor beta subunit leads to a natural killer cell-deficient form of severe combined immunodeficiency.

Gilmour KC, Fujii H, Cranston T, Davies EG, Kinnon C, Gaspar HB. Gilmour KC, et al. Among authors: gaspar hb. Blood. 2001 Aug 1;98(3):877-9. doi: 10.1182/blood.v98.3.877. Blood. 2001. PMID: 11468191 Free article.

8

X-linked lymphoproliferative disease: three atypical cases.

Nistala K, Gilmour KC, Cranston T, Davies EG, Goldblatt D, Gaspar HB, Jones AM. Nistala K, et al. Among authors: gaspar hb. Clin Exp Immunol. 2001 Oct;126(1):126-30. doi: 10.1046/j.1365-2249.2001.01599.x. Clin Exp Immunol. 2001. PMID: 11678908 Free PMC article.

9

T cell transduction and suicide with an enhanced mutant thymidine kinase.

Qasim W, Thrasher AJ, Buddle J, Kinnon C, Black ME, Gaspar HB. Qasim W, et al. Among authors: gaspar hb. Gene Ther. 2002 Jun;9(12):824-7. doi: 10.1038/sj.gt.3301690. Gene Ther. 2002. PMID: 12040465

10

X-linked lymphoproliferative disease: clinical, diagnostic and molecular perspective.

Gaspar HB, Sharifi R, Gilmour KC, Thrasher AJ. Gaspar HB, et al. Br J Haematol. 2002 Dec;119(3):585-95. doi: 10.1046/j.1365-2141.2002.03851.x. Br J Haematol. 2002. PMID: 12437631 Free article. Review. No abstract available.

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