Gaspar HB - Search Results

1

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.

2

Absence of expression of the Wiskott-Aldrich syndrome protein in peripheral blood cells of Wiskott-Aldrich syndrome patients.

MacCarthy-Morrogh L, Gaspar HB, Wang YC, Katz F, Thompson L, Layton M, Jones AM, Kinnon C. MacCarthy-Morrogh L, et al. Among authors: gaspar hb. Clin Immunol Immunopathol. 1998 Jul;88(1):22-7. doi: 10.1006/clin.1998.4557. Clin Immunol Immunopathol. 1998. PMID: 9683546

3

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.

4

Immunogenetics: changing the face of immunodeficiency.

Jones AM, Gaspar HB. Jones AM, et al. Among authors: gaspar hb. J Clin Pathol. 2000 Jan;53(1):60-5. doi: 10.1136/jcp.53.1.60. J Clin Pathol. 2000. PMID: 10767859 Free PMC article. Review.

5

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.

6

Nonmyeloablative stem cell transplantation for congenital immunodeficiencies.

Amrolia P, Gaspar HB, Hassan A, Webb D, Jones A, Sturt N, Mieli-Vergani G, Pagliuca A, Mufti G, Hadzic N, Davies G, Veys P. Amrolia P, et al. Among authors: gaspar hb. Blood. 2000 Aug 15;96(4):1239-46. Blood. 2000. PMID: 10942363 Free article.

7

Rapid protein-based assays for the diagnosis of T-B+ severe combined immunodeficiency.

Gilmour KC, Cranston T, Loughlin S, Gwyther J, Lester T, Espanol T, Hernandez M, Savoldi G, Davies EG, Abinun M, Kinnon C, Jones A, Gaspar HB. Gilmour KC, et al. Among authors: gaspar hb. Br J Haematol. 2001 Mar;112(3):671-6. doi: 10.1046/j.1365-2141.2001.02578.x. Br J Haematol. 2001. PMID: 11260071 Free article.

8

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.

9

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

10

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.

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