Richards SJ - Search Results

1

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

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

2

The glycosylphosphatidylinositol anchor and paroxysmal nocturnal haemoglobinuria/aplasia model.

Hall C, Richards SJ, Hillmen P. Hall C, et al. Among authors: richards sj. Acta Haematol. 2002;108(4):219-30. doi: 10.1159/000065658. Acta Haematol. 2002. PMID: 12432218 Review.

3

Recent advances in the diagnosis, monitoring, and management of patients with paroxysmal nocturnal hemoglobinuria.

Richards SJ, Hill A, Hillmen P. Richards SJ, et al. Cytometry B Clin Cytom. 2007 Sep;72(5):291-8. doi: 10.1002/cyto.b.20358. Cytometry B Clin Cytom. 2007. PMID: 17549742 Free article. Review.

4

Immunophenotypic analysis of PNH cells.

Richards SJ, Hillmen P. Richards SJ, et al. Curr Protoc Cytom. 2002 May;Chapter 6:Unit 6.11. doi: 10.1002/0471142956.cy0611s20. Curr Protoc Cytom. 2002. PMID: 18770768

5

Development and evaluation of a stabilized whole-blood preparation as a process control material for screening of paroxysmal nocturnal hemoglobinuria by flow cytometry.

Richards SJ, Whitby L, Cullen MJ, Dickinson AJ, Granger V, Reilly JT, Hillmen P, Barnett D. Richards SJ, et al. Cytometry B Clin Cytom. 2009 Jan;76(1):47-55. doi: 10.1002/cyto.b.20438. Epub 2008 Sep 5. Cytometry B Clin Cytom. 2009. PMID: 18777525 Free article.

6

Immunophenotypic assessment of PNH clones in major and minor cell lineages in the peripheral blood of patients with paroxysmal nocturnal hemoglobinuria.

Richards SJ, Dickinson AJ, Newton DJ, Hillmen P. Richards SJ, et al. Cytometry B Clin Cytom. 2022 Nov;102(6):487-497. doi: 10.1002/cyto.b.22094. Epub 2022 Sep 22. Cytometry B Clin Cytom. 2022. PMID: 36134740 Free article.

7

Circulating primitive stem cells in paroxysmal nocturnal hemoglobinuria (PNH) are predominantly normal in phenotype but granulocyte colony-stimulating factor treatment mobilizes mainly PNH stem cells.

Johnson RJ, Rawstron AC, Richards S, Morgan GJ, Norfolk DR, Hillmen SO. Johnson RJ, et al. Blood. 1998 Jun 15;91(12):4504-8. Blood. 1998. PMID: 9616145 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: richards s. 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

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

Richards SJ, Norfolk DR, Swirsky DM, Hillmen P. Richards SJ, et al. 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. Blood. 1999 Oct 15;94(8):2790-9. Blood. 1999. PMID: 10515882 Free article.

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