Hillmen P - Search Results

1

The management of pregnancy in paroxysmal nocturnal haemoglobinuria on long term eculizumab.

Kelly R, Arnold L, Richards S, Hill A, Bomken C, Hanley J, Loughney A, Beauchamp J, Khursigara G, Rother RP, Chalmers E, Fyfe A, Fitzsimons E, Nakamura R, Gaya A, Risitano AM, Schubert J, Norfolk D, Simpson N, Hillmen P. Kelly R, et al. Among authors: hillmen p. Br J Haematol. 2010 May;149(3):446-50. doi: 10.1111/j.1365-2141.2010.08099.x. Epub 2010 Feb 11. Br J Haematol. 2010. PMID: 20151973 Free article.

2

Two distinct patterns of glycosylphosphatidylinositol (GPI) linked protein deficiency in the red cells of patients with paroxysmal nocturnal haemoglobinuria.

Hillmen P, Hows JM, Luzzatto L. Hillmen P, et al. Br J Haematol. 1992 Mar;80(3):399-405. doi: 10.1111/j.1365-2141.1992.tb08151.x. Br J Haematol. 1992. PMID: 1374629

3

Primary thrombocythaemia in pregnancy.

Beard J, Hillmen P, Anderson CC, Lewis SM, Pearson TC. Beard J, et al. Among authors: hillmen p. Br J Haematol. 1991 Mar;77(3):371-4. doi: 10.1111/j.1365-2141.1991.tb08586.x. Br J Haematol. 1991. PMID: 2012762 Review.

4

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.

5

Mutations in the PIG-A gene causing partial deficiency of GPI-linked surface proteins (PNH II) in patients with paroxysmal nocturnal haemoglobinuria.

Bessler M, Mason PJ, Hillmen P, Luzzatto L. Bessler M, et al. Among authors: hillmen p. Br J Haematol. 1994 Aug;87(4):863-6. doi: 10.1111/j.1365-2141.1994.tb06754.x. Br J Haematol. 1994. PMID: 7986731

6

Tissue plasminogen activator for hepatic vein thrombosis in paroxysmal nocturnal haemoglobinuria.

McMullin MF, Hillmen P, Jackson J, Ganly P, Luzzatto L. McMullin MF, et al. Among authors: hillmen p. J Intern Med. 1994 Jan;235(1):85-9. doi: 10.1111/j.1365-2796.1994.tb01037.x. J Intern Med. 1994. PMID: 8283166

7

Serum erythropoietin levels in paroxysmal nocturnal haemoglobinuria: implications for therapy.

McMullin MF, Hillmen P, Elder GE, Lappin TR, Luzzatto L. McMullin MF, et al. Among authors: hillmen p. Br J Haematol. 1996 Mar;92(4):815-7. doi: 10.1046/j.1365-2141.1996.421961.x. Br J Haematol. 1996. PMID: 8616071

8

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.

9

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.

10

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.

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