Hillmen P - Search Results

1

Analysis of T cells in paroxysmal nocturnal hemoglobinuria provides direct evidence that thymic T-cell production declines with age.

Richards SJ, Morgan GJ, Hillmen P. Richards SJ, et al. Among authors: hillmen p. Blood. 1999 Oct 15;94(8):2790-9. Blood. 1999. PMID: 10515882 Free article.

2

Clonal origin of abnormal granulocytes in paroxysmal nocturnal hemoglobinuria.

Bessler M, Hillmen P, Luzzatto L. Bessler M, et al. Among authors: hillmen p. Blood. 1992 Aug 1;80(3):844-5. Blood. 1992. PMID: 1638035 Free article. No abstract available.

3

Expression of recombinant transmembrane CD59 in paroxysmal nocturnal hemoglobinuria B cells confers resistance to human complement.

Rother RP, Rollins SA, Mennone J, Chodera A, Fidel SA, Bessler M, Hillmen P, Squinto SP. Rother RP, et al. Among authors: hillmen p. Blood. 1994 Oct 15;84(8):2604-11. Blood. 1994. PMID: 7522635 Free article.

4

Production and characterization of lymphoblastoid cell lines with the paroxysmal nocturnal hemoglobinuria phenotype.

Hillmen P, Bessler M, Crawford DH, Luzzatto L. Hillmen P, et al. Blood. 1993 Jan 1;81(1):193-9. Blood. 1993. PMID: 7678064 Free article.

5

Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type.

Nafa K, Mason PJ, Hillmen P, Luzzatto L, Bessler M. Nafa K, et al. Among authors: hillmen p. Blood. 1995 Dec 15;86(12):4650-5. Blood. 1995. PMID: 8541557 Free article.

6

Both paroxysmal nocturnal hemoglobinuria (PNH) type II cells and PNH type III cells can arise from different point mutations involving the same codon of the PIG-A gene.

Rollinson S, Richards S, Norfolk D, Bibi K, Morgan G, Hillmen P. Rollinson S, et al. Among authors: hillmen p. Blood. 1997 Apr 15;89(8):3069-71. Blood. 1997. PMID: 9108434 Free article. No abstract available.

7

Lymphocyte subset analysis and glycosylphosphatidylinositol phenotype in patients with paroxysmal nocturnal hemoglobinuria.

Richards SJ, Norfolk DR, Swirsky DM, Hillmen P. Richards SJ, et al. Among authors: hillmen p. Blood. 1998 Sep 1;92(5):1799-806. Blood. 1998. PMID: 9716611 Free article.

8

The PNH phenotype cells that emerge in most patients after CAMPATH-1H therapy are present prior to treatment.

Rawstron AC, Rollinson SJ, Richards S, Short MA, English A, Morgan GJ, Hale G, Hillmen P. Rawstron AC, et al. Among authors: hillmen p. Br J Haematol. 1999 Oct;107(1):148-53. doi: 10.1046/j.1365-2141.1999.01676.x. Br J Haematol. 1999. PMID: 10520035 Free article.

9

Implications of recent insights into the pathophysiology of paroxysmal nocturnal haemoglobinuria.

Hillmen P, Richards SJ. Hillmen P, et al. Br J Haematol. 2000 Mar;108(3):470-9. doi: 10.1046/j.1365-2141.2000.01802.x. Br J Haematol. 2000. PMID: 10759701 Free article. Review. No abstract available.

10

Application of flow cytometry to the diagnosis of paroxysmal nocturnal hemoglobinuria.

Richards SJ, Rawstron AC, Hillmen P. Richards SJ, et al. Among authors: hillmen p. Cytometry. 2000 Aug 15;42(4):223-33. Cytometry. 2000. PMID: 10934341 Review.

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