Hillmen P - Search Results

1

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

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

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

Natural history of paroxysmal nocturnal hemoglobinuria.

Hillmen P, Lewis SM, Bessler M, Luzzatto L, Dacie JV. Hillmen P, et al. N Engl J Med. 1995 Nov 9;333(19):1253-8. doi: 10.1056/NEJM199511093331904. N Engl J Med. 1995. PMID: 7566002 Free article.

5

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.

6

Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria.

Bessler M, Mason P, Hillmen P, Luzzatto L. Bessler M, et al. Among authors: hillmen p. Lancet. 1994 Apr 16;343(8903):951-3. doi: 10.1016/s0140-6736(94)90068-x. Lancet. 1994. PMID: 7909012

7

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

8

Genomic organization of the X-linked gene (PIG-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related autosomal pseudogene mapped to 12q21.

Bessler M, Hillmen P, Longo L, Luzzatto L, Mason PJ. Bessler M, et al. Among authors: hillmen p. Hum Mol Genet. 1994 May;3(5):751-7. doi: 10.1093/hmg/3.5.751. Hum Mol Genet. 1994. PMID: 8081362

9

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

10

Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene.

Bessler M, Mason PJ, Hillmen P, Miyata T, Yamada N, Takeda J, Luzzatto L, Kinoshita T. Bessler M, et al. Among authors: hillmen p. EMBO J. 1994 Jan 1;13(1):110-7. doi: 10.1002/j.1460-2075.1994.tb06240.x. EMBO J. 1994. PMID: 8306954 Free PMC article.

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