-
1
-
-
0028299834
-
Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria
-
Besslcr. M.. Mason, P., Hillmen, P. & Luzzatto, L. (1994) Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria. Lancet, 343, 951-953.
-
(1994)
Lancet
, vol.343
, pp. 951-953
-
-
Besslcr, M.1
Mason, P.2
Hillmen, P.3
Luzzatto, L.4
-
2
-
-
0015457605
-
Paroxysmal nocturnal haemoglobinuria: Clinical manifestations, haematology, and nature of the disease
-
Dacie, J.V. & Lewis, S.M. (1972) Paroxysmal nocturnal haemoglobinuria: clinical manifestations, haematology, and nature of the disease. Series Haeinatologica, 5, 3-23.
-
(1972)
Series Haeinatologica
, vol.5
, pp. 3-23
-
-
Dacie, J.V.1
Lewis, S.M.2
-
3
-
-
0029032667
-
Flow cytometric analysis of decay-accelerating factor (CD55) on neutrophils from aplastic anaemia patients
-
Fores. R., Alcocer. M., Diez-Martin, J.L. & Fernandez. M.N. (1995) Flow cytometric analysis of decay-accelerating factor (CD55) on neutrophils from aplastic anaemia patients. British Journal of Ilaematologij. 90. 728-730.
-
(1995)
British Journal of Ilaematologij.
, vol.90
, pp. 728-730
-
-
Fores, R.1
Alcocer, M.2
Diez-Martin, J.L.3
Fernandez, M.N.4
-
4
-
-
0028962569
-
Aplastic anemia and paroxysmal nocturnal hemoglobinuria: Search for a pathogenetic link
-
Griscelli-Bennaceur, A., Gluckman, E., Scrobohaci, M.L., Jonveaux, P., Vu, T., Bazarbachi, A., Carosella. E.D., Sigaux, F. & Socie, G. (1995) Aplastic anemia and paroxysmal nocturnal hemoglobinuria: search for a pathogenetic link. Blood, 85,1354-1363.
-
(1995)
Blood
, pp. 1354-1363
-
-
Griscelli-Bennaceur, A.1
Gluckman, E.2
Scrobohaci, M.L.3
Jonveaux, P.4
Vu, T.5
Bazarbachi, A.6
Carosella, E.D.7
Sigaux, F.8
Socie, G.9
-
5
-
-
0028290901
-
Characterization of genomic PIG-A gene: A gene for glycosylphosphatidylinositol-anchor biosynthesis and paroxysmal nocturnal hemoglobinuria
-
Iida, Y., Takeda. J., Miyata. T.. Inoue. N.. Nishimurîi. J., Kitani, T., Maeda, K. & Kinoshita, T. (1994) Characterization of genomic PIG-A gene: a gene for glycosylphosphatidylinositol-anchor biosynthesis and paroxysmal nocturnal hemoglobinuria. Blood, 83. 3126-3131.
-
(1994)
Blood
, vol.83
, pp. 3126-3131
-
-
Iida, Y.1
Takeda, J.2
Miyata, T.3
Inoue, N.4
Nishimurîi, J.5
Kitani, T.6
Maeda, K.7
Kinoshita, T.8
-
6
-
-
0023784162
-
Different distribution of decay-accelerating factor on hematopoietic progenitors from normal individuals and patients with paroxysmal nocturnal hemoglobinuria
-
Kanamaru, A., Okuda, K., Ueda, E., Kitani, T., Kinoshita, T. & Nagai, K. (1988) Different distribution of decay-accelerating factor on hematopoietic progenitors from normal individuals and patients with paroxysmal nocturnal hemoglobinuria. Blood, 72, 507-511.
-
(1988)
Blood
, vol.72
, pp. 507-511
-
-
Kanamaru, A.1
Okuda, K.2
Ueda, E.3
Kitani, T.4
Kinoshita, T.5
Nagai, K.6
-
7
-
-
0030932540
-
-
Luzzatto. L., Bessler, M. & Rotoli, B. (1997) Somatic mutations in paroxysmal nocturnal hemoglobinuria: a blessing in disguise? Cell, 88, 1-4.
-
(1997)
Somatic Mutations in Paroxysmal Nocturnal Hemoglobinuria: a Blessing in Disguise? Cell
, vol.88
, pp. 1-4
-
-
Luzzatto, L.1
Bessler, M.2
Rotoli, B.3
-
8
-
-
33847519081
-
-
Maciejewski, J.P.. Sloand, E.M., Sato, T., Andersen, S. & Young, N.S. (1997) Impaired hematopoiesis in paroxysmal nocturnal
-
(1997)
Impaired Hematopoiesis in Paroxysmal Nocturnal
-
-
Maciejewski, J.P.1
Sloand, E.M.2
Sato, T.3
Andersen, S.4
Young, N.S.5
-
9
-
-
0031042052
-
-
hemoglobinuria/aplastic anemia is not associated with a selective proliferative defect in the glycosylphosphatidylinositol-anchored protein-deficient clone. Blood, 89, 1173-1181.
-
(1173)
, pp. 1181
-
-
Blood, B.1
-
10
-
-
0028944403
-
Paroxysmal nocturnal hemoglobinuria clone in bone marrow of patients with pancytopenia
-
Nakakuma, H., Nagakura, S.. Iwamoto. N.. Kawaguchi. T., Hidaka, M.. Horikawa, K., Kagimoto, X, Shido, T. & Takatsuki, K. (1995) Paroxysmal nocturnal hemoglobinuria clone in bone marrow of patients with pancytopenia. Blood, 85, 1371-1376.
-
(1995)
Blood
, vol.85
, pp. 1371-1376
-
-
Nakakuma, H.1
Nagakura, S.2
Iwamoto, N.3
Kawaguchi, T.4
Hidaka, M.5
Horikawa, K.6
Kagimoto, X.7
Shido, T.8
Takatsuki, K.9
-
11
-
-
0030942613
-
A patient with paroxysmal nocturnal hemoglobinuria bearing four independent PIG-A mutant clones
-
Nishimura, J., Inoue, N., \Vada, H., Ueda, E., Pramoonjago, P., Hirota, T., Machii. T., Kageyama, T., Kanamaru, A., Takeda. J., Kinoshita, T. & Kitani. T. (1997) A patient with paroxysmal nocturnal hemoglobinuria bearing four independent PIG-A mutant clones. Blood. 89, 3470-3476.
-
(1997)
Blood.
, vol.89
, pp. 3470-3476
-
-
Nishimura, J.1
Inoue, N.2
Vada, H.3
Ueda, E.4
Pramoonjago, P.5
Hirota, T.6
Machii, T.7
Kageyama, T.8
Kanamaru, A.9
Takeda, J.10
Kinoshita, T.11
Kitani, T.12
-
12
-
-
0029054191
-
Flow cytometric analysis of homologous restriction factor 20 kD (HRF20) expression on progeny cells during differentiation from haemopoietic progenitors in paroxysmal nocturnal haemoglobinuria
-
Nishimura, T.. Kanamaru, A., Kakishita, E. & Nagai, K. (1995) Flow cytometric analysis of homologous restriction factor 20 kD (HRF20) expression on progeny cells during differentiation from haemopoietic progenitors in paroxysmal nocturnal haemoglobinuria. British Journal of Haematology. 90, 293-299.
-
(1995)
British Journal of Haematology.
, vol.90
, pp. 293-299
-
-
Nishimura, T.1
Kanamaru, A.2
Kakishita, E.3
Nagai, K.4
-
13
-
-
0025243780
-
Expression of decay-accelerating factor on hematopoietic progenitors and their progeny cells grown in cultures with fractionated bone marrow cells from normal individuals and patients with paroxysmal nocturnal hemoglobinuria
-
Okuda, K., Kanamaru, A., Ueda, E., Kitani, T., Okada, N.. Okada. H., Kakishita, E. & Nagai, K. (1990) Expression of decay-accelerating factor on hematopoietic progenitors and their progeny cells grown in cultures with fractionated bone marrow cells from normal individuals and patients with paroxysmal nocturnal hemoglobinuria. Experimental Hematology. 18, 1132-1136.
-
(1990)
Experimental Hematology.
, vol.18
, pp. 1132-1136
-
-
Okuda, K.1
Kanamaru, A.2
Ueda, E.3
Kitani, T.4
Okada, N.5
Okada, H.6
Kakishita, E.7
Nagai, K.8
-
14
-
-
0021170116
-
Two populations of erythroid cell progenitors in paroxysmal nocturnal hemoglobinuria
-
Rotoli, B., Robledo, R., Scarpato, N. & Luzzatto, L. (1984) Two populations of erythroid cell progenitors in paroxysmal nocturnal hemoglobinuria. Blood, 64, 847-851.
-
(1984)
Blood
, vol.64
, pp. 847-851
-
-
Rotoli, B.1
Robledo, R.2
Scarpato, N.3
Luzzatto, L.4
-
15
-
-
0028897137
-
A pathogenetic link between aplastic anemia and paroxysmal nocturnal hemoglobinuria is suggested by a high frequency of aplastic anemia patients with a deficiency of phosphatidylinositol glycan anchored proteins
-
Schrezenmeier, H., Hertenstein, B., Wagner, B., Raghavachar, A. & Heimpel, II. (1995) A pathogenetic link between aplastic anemia and paroxysmal nocturnal hemoglobinuria is suggested by a high frequency of aplastic anemia patients with a deficiency of phosphatidylinositol glycan anchored proteins. Experimental Eematology, 23, 81-87.
-
(1995)
Experimental Eematology
, vol.23
, pp. 81-87
-
-
Schrezenmeier, H.1
Hertenstein, B.2
Wagner, B.3
Raghavachar, A.4
Heimpel, I.I.5
-
16
-
-
0028295447
-
Development of the glycosylphosphatidylinositol-anchoring defect characteristic for paroxysmal nocturnal hemoglobinuria in patients with aplastic anemia
-
Schubert, J., Vogt, H.G., Zielinska-Skowronek, M., Freund, M., Kaltwasser, J.P., Hoetzer, D. & Schmidt, R.E. (1994) Development of the glycosylphosphatidylinositol-anchoring defect characteristic for paroxysmal nocturnal hemoglobinuria in patients with aplastic anemia. Blood, 83, 2323-2328.
-
(1994)
Blood
, vol.83
, pp. 2323-2328
-
-
Schubert, J.1
Vogt, H.G.2
Zielinska-Skowronek, M.3
Freund, M.4
Kaltwasser, J.P.5
Hoetzer, D.6
Schmidt, R.E.7
-
17
-
-
0027310539
-
Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria
-
Takeda, J.. Miyata, T., Kawagoe, K., lida. Y., Endo, Y., Fujita, T., Takahashi, M., Kitani, T. & Kinoshita, T. (1993) Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria. Cell, 73, 703-711.
-
(1993)
Cell
, vol.73
, pp. 703-711
-
-
Takeda, J.1
Miyata, T.2
Kawagoe, K.3
Lida, Y.4
Endo, Y.5
Fujita, T.6
Takahashi, M.7
Kitani, T.8
Kinoshita, T.9
-
18
-
-
0026596863
-
The problem of clonality in aplastic anemia: Dr Dameshek's riddle, restated
-
Young, N.S. (1992) The problem of clonality in aplastic anemia: Dr Dameshek's riddle, restated. Blood, 79, 1385-1392.
-
(1992)
Blood
, vol.79
, pp. 1385-1392
-
-
Young, N.S.1
|