Rosse WF - Search Results

1

A case report: IgG autoanti-N as a cause of severe autoimmune hemolytic anemia.

Combs MR, Telen MJ, Hall SE, Rosse WF. Combs MR, et al. Among authors: rosse wf. Immunohematology. 1990;6(4):83-6. Immunohematology. 1990. PMID: 15946002

2

Captopril-enhanced binding of PlA1 (HPA-1a) antibodies in posttransfusion purpura.

Bepler G, Hoffman SE, Thompson BP, Telen MJ, Rosse WF. Bepler G, et al. Among authors: rosse wf. Transfusion. 1991 Oct;31(8):752-5. doi: 10.1046/j.1537-2995.1991.31892023503.x. Transfusion. 1991. PMID: 1926322

3

Identification of human erythrocyte blood group antigens on decay-accelerating factor (DAF) and an erythrocyte phenotype negative for DAF.

Telen MJ, Hall SE, Green AM, Moulds JJ, Rosse WF. Telen MJ, et al. Among authors: rosse wf. J Exp Med. 1988 Jun 1;167(6):1993-8. doi: 10.1084/jem.167.6.1993. J Exp Med. 1988. PMID: 2455016 Free PMC article.

4

The use of monoclonal antibodies and flow cytometry in the diagnosis of paroxysmal nocturnal hemoglobinuria.

Hall SE, Rosse WF. Hall SE, et al. Among authors: rosse wf. Blood. 1996 Jun 15;87(12):5332-40. Blood. 1996. PMID: 8652849 Free article.

5

Evidence that several high-frequency human blood group antigens reside on phosphatidylinositol-linked erythrocyte membrane proteins.

Telen MJ, Rosse WF, Parker CJ, Moulds MK, Moulds JJ. Telen MJ, et al. Among authors: rosse wf. Blood. 1990 Apr 1;75(7):1404-7. Blood. 1990. PMID: 2317557 Free article.

6

Immunophenotypic analysis of reticulocytes in paroxysmal nocturnal hemoglobinuria.

Ware RE, Rosse WF, Hall SE. Ware RE, et al. Among authors: rosse wf. Blood. 1995 Aug 15;86(4):1586-9. Blood. 1995. PMID: 7543308 Free article.

7

Paroxysmal nocturnal hemoglobinuria with onset in childhood and adolescence.

Ware RE, Hall SE, Rosse WF. Ware RE, et al. Among authors: rosse wf. N Engl J Med. 1991 Oct 3;325(14):991-6. doi: 10.1056/NEJM199110033251403. N Engl J Med. 1991. PMID: 1886636 Free article.

8

Glycosyl-phosphatidylinositol anchor synthesis in paroxysmal nocturnal hemoglobinuria: partial or complete defect in an early step.

Norris J, Hall S, Ware RE, Kamitani T, Chang HM, Yeh E, Rosse WF. Norris J, et al. Among authors: rosse wf. Blood. 1994 Feb 1;83(3):816-21. Blood. 1994. PMID: 7507735 Free article.

9

Defective glycosylphosphatidylinositol anchor synthesis in paroxysmal nocturnal hemoglobinuria granulocytes.

Mahoney JF, Urakaze M, Hall S, DeGasperi R, Chang HM, Sugiyama E, Warren CD, Borowitz M, Nicholson-Weller A, Rosse WF, et al. Mahoney JF, et al. Among authors: rosse wf. Blood. 1992 Mar 15;79(6):1400-3. Blood. 1992. PMID: 1372185 Free article.

10

Separation of the acetylcholinesterase-deficient red cells in paroxysmal nocturnal hemoglobinuria.

Chow FL, Hall SE, Rosse WF, Telen MJ. Chow FL, et al. Among authors: rosse wf. Blood. 1986 Apr;67(4):893-7. Blood. 1986. PMID: 3955235 Free article.

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