-
1
-
-
0001194004
-
Chronic hemolytic anemia with paroxysmal nocturnal haemoglobinuria. a study of the mechanism of hemolysis in relation to acid-base equilibrium
-
Ham TH. Chronic hemolytic anemia with paroxysmal nocturnal haemoglobinuria. A study of the mechanism of hemolysis in relation to acid-base equilibrium. N Engl J Med 1937;217:915.
-
(1937)
N Engl J Med
, vol.217
, pp. 915
-
-
Ham, T.H.1
-
2
-
-
50349141511
-
Paroxysmal nocturnal haemoglobinuria of the Marchiafava type
-
Dacie JV, Israels MCG, Wilkinson JF. Paroxysmal nocturnal haemoglobinuria of the Marchiafava type. Lancet 1938,1:479.
-
(1938)
Lancet
, vol.1
, pp. 479
-
-
Dacie, J.V.1
Israels, M.C.G.2
Wilkinson, J.F.3
-
3
-
-
0000035046
-
Paroxysmal nocturnal haemoglobinuria
-
Dacie JV. Paroxysmal nocturnal haemoglobinuria. Proc Roy Soc Med 1963;56:587.
-
(1963)
Proc Roy Soc Med
, vol.56
, pp. 587
-
-
Dacie, J.V.1
-
4
-
-
0014832992
-
Paroxysmal nocturnal haemoglobinuria: Evidence for monoclonal origin of abnormal red cells
-
Oni SB, Osunkoya BO, Luzzatto L. Paroxysmal nocturnal haemoglobinuria: evidence for monoclonal origin of abnormal red cells. Blood 1970;36:145.
-
(1970)
Blood
, vol.36
, pp. 145
-
-
Oni, S.B.1
Osunkoya, B.O.2
Luzzatto, L.3
-
5
-
-
0021170116
-
Two populations of erythroid cell progenitors in paroxysmal nocturnal haemoglobinuria
-
Rotoli B, Robledo R, Scarpato N, Luzzatto L. Two populations of erythroid cell progenitors in paroxysmal nocturnal haemoglobinuria. Blood 1984;64:847.
-
(1984)
Blood
, vol.64
, pp. 847
-
-
Rotoli, B.1
Robledo, R.2
Scarpato, N.3
Luzzatto, L.4
-
6
-
-
0028224269
-
Genomic organization of the X-linked gene (PGI-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related pseudogene mapped to 12q21
-
Bessler M, Hillmen P, Longo L, Luzzatto L, Mason PJ: Genomic organization of the X-linked gene (PGI-A) that is mutated in paroxysmal nocturnal haemoglobinuria and of a related pseudogene mapped to 12q21. Hum Mol Genet 1994;3:751.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 751
-
-
Bessler, M.1
Hillmen, P.2
Longo, L.3
Luzzatto, L.4
Mason, P.J.5
-
7
-
-
0027310539
-
Deficiency of the PIG-A gene in paroxysmal nocturnal haemoglobinuria
-
Takeda J, Miyata T, Kawagoe K, Kinoshita T. Deficiency of the PIG-A gene in paroxysmal nocturnal haemoglobinuria. Cell 1993;73:703.
-
(1993)
Cell
, vol.73
, pp. 703
-
-
Takeda, J.1
Miyata, T.2
Kawagoe, K.3
Kinoshita, T.4
-
8
-
-
0028057807
-
Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene
-
Bessler M, Mason PJ, Hillmen P, Miyata T, Yamada N, Luzzatto L, Kinoshitat T. Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene. EMBO J 1994;13:110-117.
-
(1994)
EMBO J
, vol.13
, pp. 110-117
-
-
Bessler, M.1
Mason, P.J.2
Hillmen, P.3
Miyata, T.4
Yamada, N.5
Luzzatto, L.6
Kinoshitat, T.7
-
9
-
-
85084770434
-
Mutations in the PIG-A gene causing paroxysmal nocturnal haemoglobinuria (PNH) are mainly of the frameshift type
-
in press
-
Nafa K, Mason PJ, Hillmen P, Luzzatto L, Bessler M: Mutations in the PIG-A gene causing paroxysmal nocturnal haemoglobinuria (PNH) are mainly of the frameshift type. Blood (in press).
-
Blood
-
-
Nafa, K.1
Mason, P.J.2
Hillmen, P.3
Luzzatto, L.4
Bessler, M.5
-
10
-
-
0028353422
-
Mutations within the PIG-A gene in patients with paroxysmal nocturnal haemoglobinuria
-
Ware RE, Rosee WF, Howard TA. Mutations within the PIG-A gene in patients with paroxysmal nocturnal haemoglobinuria. Blood 1994;83:2418.
-
(1994)
Blood
, vol.83
, pp. 2418
-
-
Ware, R.E.1
Rosee, W.F.2
Howard, T.A.3
-
11
-
-
85088325432
-
Somatic mutations in the PIG-A gene found in Japaneese patients with paroxysmal nocturnal haemoglobinuria
-
in press
-
Yamada N, Miyata T, Maeda K, Kitani T, Takeda J, Kinoshita T. Somatic mutations in the PIG-A gene found in Japaneese patients with paroxysmal nocturnal haemoglobinuria. Blood (in press).
-
Blood
-
-
Yamada, N.1
Miyata, T.2
Maeda, K.3
Kitani, T.4
Takeda, J.5
Kinoshita, T.6
-
12
-
-
0025866225
-
fc-gama-III receptors (FcRIII) on granulocytes: A new specific and sensitive test for paroxysmal nocturnal haemoglobinuria
-
Bessler M, Fehr J. fc-gama-III receptors (FcRIII) on granulocytes: a new specific and sensitive test for paroxysmal nocturnal haemoglobinuria. Eur J Haematol 1991;47:179.
-
(1991)
Eur J Haematol
, vol.47
, pp. 179
-
-
Bessler, M.1
Fehr, J.2
-
14
-
-
0025062074
-
The PIG-anchoring defect in NK lymphocytes of PNH patients
-
Schubert J, Uchiechowski P, Delany P, Tischler HJ, Kolanus W, Schmidt RE. The PIG-anchoring defect in NK lymphocytes of PNH patients. Blood 1990;76:1181.
-
(1990)
Blood
, vol.76
, pp. 1181
-
-
Schubert, J.1
Uchiechowski, P.2
Delany, P.3
Tischler, H.J.4
Kolanus, W.5
Schmidt, R.E.6
-
15
-
-
0028802443
-
Long-term follow up, survival and self-cure of a cohort of 80 patients with paroxysmal nocturnal haemoglobinuria
-
Hillmen P, Lewis SM, Bessler M, Luzzatto L, Davie JV. Long-term follow up, survival and self-cure of a cohort of 80 patients with paroxysmal nocturnal haemoglobinuria. N Engl J Med 1995;33:1253.
-
(1995)
N Engl J Med
, vol.33
, pp. 1253
-
-
Hillmen, P.1
Lewis, S.M.2
Bessler, M.3
Luzzatto, L.4
Davie, J.V.5
-
16
-
-
0023789856
-
Late haematological complications in severe aplastic anaemia
-
Tichelli A, Gratwohl A, Wurschl A, Nissen C, Speck B: Late haematological complications in severe aplastic anaemia. Br J Haematol 1988;69:413.
-
(1988)
Br J Haematol
, vol.69
, pp. 413
-
-
Tichelli, A.1
Gratwohl, A.2
Wurschl, A.3
Nissen, C.4
Speck, B.5
-
17
-
-
0016466742
-
Paroxysmal nocturnal haemoglobinuria
-
Sirchia G, Lewis SM. Paroxysmal nocturnal haemoglobinuria. Clin Haematol 1975;4:199.
-
(1975)
Clin Haematol
, vol.4
, pp. 199
-
-
Sirchia, G.1
Lewis, S.M.2
-
18
-
-
0025053264
-
Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal haemoglobinuria
-
Yamashina N, Ueda E, Kinoshita T, Takami T, Ojima A, Ono H, Tanaka H, Kondo N, Orii T, Okada N, Okada H, Inoue K, Kitani T. Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal haemoglobinuria. N Engl J Med 1990;323:1184.
-
(1990)
N Engl J Med
, vol.323
, pp. 1184
-
-
Yamashina, N.1
Ueda, E.2
Kinoshita, T.3
Takami, T.4
Ojima, A.5
Ono, H.6
Tanaka, H.7
Kondo, N.8
Orii, T.9
Okada, N.10
Okada, H.11
Inoue, K.12
Kitani, T.13
-
19
-
-
0029887115
-
The dual pathogenesis of paroxysmal nocturnal hemoglobinuria
-
Luzzatto L, Bessler M. The dual pathogenesis of paroxysmal nocturnal hemoglobinuria. Curr Opin Hemat 1996;3:101.
-
(1996)
Curr Opin Hemat
, vol.3
, pp. 101
-
-
Luzzatto, L.1
Bessler, M.2
-
20
-
-
0026537310
-
Two distinct patterns of glycosylphosphatidylinositol (GPI) linked protein deficiency demonstrable in the red cells of patients with paroxysmal nocturnal haemoglobinuria
-
Hillmen P, Hows JW, Luzzatto L. Two distinct patterns of glycosylphosphatidylinositol (GPI) linked protein deficiency demonstrable in the red cells of patients with paroxysmal nocturnal haemoglobinuria. Br J Haematol 1992;80:399.
-
(1992)
Br J Haematol
, vol.80
, pp. 399
-
-
Hillmen, P.1
Hows, J.W.2
Luzzatto, L.3
-
21
-
-
0026588963
-
Marrow transplantation for paroxysmal nocturnal haemoglobinuria
-
Kawahara K, Witherspoon RP, Storb R: Marrow transplantation for paroxysmal nocturnal haemoglobinuria. Amer J Hematol 1992;39:283.
-
(1992)
Amer J Hematol
, vol.39
, pp. 283
-
-
Kawahara, K.1
Witherspoon, R.P.2
Storb, R.3
-
22
-
-
0028275515
-
Tissue plasminogen activator for hepatic vein thrombosis in paroxysmal nocturnal haemoglobinuria
-
McMullin MF, Hillmen P, Jackson J, Ganly P, Luzzatto L: Tissue plasminogen activator for hepatic vein thrombosis in paroxysmal nocturnal haemoglobinuria. J Int Med 1994;235:85.
-
(1994)
J Int Med
, vol.235
, pp. 85
-
-
McMullin, M.F.1
Hillmen, P.2
Jackson, J.3
Ganly, P.4
Luzzatto, L.5
-
23
-
-
0023738967
-
Complete response to antilymphocyte globulin in a case of aplastic anemia-paroxysmal nocturnal hemoglobinuria syndrome
-
Kusminsky GD, Barazzutti L, Korin JD, Blasetti A, Tartas NE, Sgnchez Avalos JC. Complete response to antilymphocyte globulin in a case of aplastic anemia-paroxysmal nocturnal hemoglobinuria syndrome [letter]. Am J Hematol 1988;29:123.
-
(1988)
Am J Hematol
, vol.29
, pp. 123
-
-
Kusminsky, G.D.1
Barazzutti, L.2
Korin, J.D.3
Blasetti, A.4
Tartas, N.E.5
Sgnchez Avalos, J.C.6
-
24
-
-
0029933457
-
Correction of aplastic anaemia, complicating paroxysmal nocturnal haemoglobinuria: Absence of eradication of the PNH clone and dependence of response on cyclosporin a administration
-
Stoppa AM, Vey N, Sainty D, Arnoulet C, Camerlo J, Cappiello MA, Gastaut JA, Maraninchi D. Correction of aplastic anaemia, complicating paroxysmal nocturnal haemoglobinuria: absence of eradication of the PNH clone and dependence of response on cyclosporin A administration. Br J Haematol 1996;93:42.
-
(1996)
Br J Haematol
, vol.93
, pp. 42
-
-
Stoppa, A.M.1
Vey, N.2
Sainty, D.3
Arnoulet, C.4
Camerlo, J.5
Cappiello, M.A.6
Gastaut, J.A.7
Maraninchi, D.8
|