-
1
-
-
0028299834
-
Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria
-
Bessler, M., Mason, P., Hillmen, P. & Luzzatto, L. (1994a) Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria. Lancet, 343, 951-952.
-
(1994)
Lancet
, vol.343
, pp. 951-952
-
-
Bessler, M.1
Mason, P.2
Hillmen, P.3
Luzzatto, L.4
-
2
-
-
0028057807
-
Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene
-
Bessler, M., Mason, P.J., Hillmen, P., Miyata, T., Yamada, N., Takeda, J., Luzzatto, L. & Kinoshita, T. (1994b) Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene. EMBO Journal, 13, 110-117.
-
(1994)
EMBO Journal
, vol.13
, pp. 110-117
-
-
Bessler, M.1
Mason, P.J.2
Hillmen, P.3
Miyata, T.4
Yamada, N.5
Takeda, J.6
Luzzatto, L.7
Kinoshita, T.8
-
3
-
-
0023104647
-
Acute myeloblastic leukemia in paroxysmal nocturnal hemoglobinuria: Evidence of evolution from the abnormal paroxysmal nocturnal hemoglobinuria clone
-
Devine, D.V., Gluck, W.L., Rosse, W.F. & Weinberg, J.B. (1987) Acute myeloblastic leukemia in paroxysmal nocturnal hemoglobinuria: evidence of evolution from the abnormal paroxysmal nocturnal hemoglobinuria clone. Journal of Clinical Investigation, 79, 314-317.
-
(1987)
Journal of Clinical Investigation
, vol.79
, pp. 314-317
-
-
Devine, D.V.1
Gluck, W.L.2
Rosse, W.F.3
Weinberg, J.B.4
-
4
-
-
0026645382
-
Multicenter randomized study comparing cyclosporin-A alone and anti-thymocyte globulin with prednisone for treatment of severe aplastic anemia
-
Gluckman, E., Esperou-Bourdeau, H., Baruchel, A., Boogaerts, M., Briere, J., Donadio, D., Leverger, G., Leporrier, M., Reiffers, J., Janvier, M., Michallet, M., Stryckmans, P., and the Cooperative Group on the Treatment of Aplastic Anemia (1992) Multicenter randomized study comparing cyclosporin-A alone and anti-thymocyte globulin with prednisone for treatment of severe aplastic anemia. Blood, 79, 2510-2546.
-
(1992)
Blood
, vol.79
, pp. 2510-2546
-
-
Gluckman, E.1
Esperou-Bourdeau, H.2
Baruchel, A.3
Boogaerts, M.4
Briere, J.5
Donadio, D.6
Leverger, G.7
Leporrier, M.8
Reiffers, J.9
Janvier, M.10
Michallet, M.11
Stryckmans, P.12
-
5
-
-
0020536466
-
Paroxysmal nocturnal hemoglobinuria and acute non-lymphocytic leukemia: A report of three cases exhibiting different cytologie types
-
Krause, J.R. (1983) Paroxysmal nocturnal hemoglobinuria and acute non-lymphocytic leukemia: a report of three cases exhibiting different cytologie types. Cancer, 51, 2078-2082.
-
(1983)
Cancer
, vol.51
, pp. 2078-2082
-
-
Krause, J.R.1
-
6
-
-
0023738967
-
Complete response to anti-lymphocyte globulin in a case of aplastic anemia-paroxysmal nocturnal hemoglubinuria syndrome
-
Kuminsky, G.D., Barazutti, L., Korin, J.D., Blasetti, A., Tartas, N.E., Sanchez, J.C. & Avalo, S. (1988) Complete response to anti-lymphocyte globulin in a case of aplastic anemia-paroxysmal nocturnal hemoglubinuria syndrome. American Journal of Hematology, 29, 123.
-
(1988)
American Journal of Hematology
, vol.29
, pp. 123
-
-
Kuminsky, G.D.1
Barazutti, L.2
Korin, J.D.3
Blasetti, A.4
Tartas, N.E.5
Sanchez, J.C.6
Avalo, S.7
-
7
-
-
0028234052
-
Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: A clonal disease originating from within a clonal disease
-
Longo, L., Bessler, M., Beris, P., Swirsky, D. & Luzzatto, L. (1994) Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal disease. British Journal of Haematology, 87, 401-403.
-
(1994)
British Journal of Haematology
, vol.87
, pp. 401-403
-
-
Longo, L.1
Bessler, M.2
Beris, P.3
Swirsky, D.4
Luzzatto, L.5
-
9
-
-
0024325872
-
Paroxysmal nocturnal hemoglobinuria
-
Rotoli, B. & Luzzatto, L. (1989) Paroxysmal nocturnal hemoglobinuria. Seminars in Hematology, 26, 201-207.
-
(1989)
Seminars in Hematology
, vol.26
, pp. 201-207
-
-
Rotoli, B.1
Luzzatto, L.2
-
10
-
-
0028012242
-
The target gene in paroxysmal nocturnal hemoglobinuria
-
Schwartz, R.S. (1994) The target gene in paroxysmal nocturnal hemoglobinuria. New England Journal of Medicine, 330, 283-284.
-
(1994)
New England Journal of Medicine
, vol.330
, pp. 283-284
-
-
Schwartz, R.S.1
-
11
-
-
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., Lido, Y., Endo, Y., Fujita, T., Takahashi, M., Kitani, T. & Kinoshita, T. (1995) Deficiency of the GPI-anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria. Cell. 73, 703-711.
-
(1995)
Cell
, vol.73
, pp. 703-711
-
-
Takeda, J.1
Miyata, T.2
Kawagoe, K.3
Lido, Y.4
Endo, Y.5
Fujita, T.6
Takahashi, M.7
Kitani, T.8
Kinoshita, T.9
-
12
-
-
0028229227
-
Myelodysplasia following paroxysmal nocturnal haemoglobinuria: Evidence for the emergence of a separate clone
-
Van Kamp, H., Smit, J.W., van den Berg, E., Halie, M.R. & Vellenga, E. (1994) Myelodysplasia following paroxysmal nocturnal haemoglobinuria: evidence for the emergence of a separate clone. British Journal of Haematology, 87, 399-400.
-
(1994)
British Journal of Haematology
, vol.87
, pp. 399-400
-
-
Van Kamp, H.1
Smit, J.W.2
Van Den Berg, E.3
Halie, M.R.4
Vellenga, E.5
|