-
1
-
-
0032323907
-
Molecular genetics and cytogenetics of myeloproliferative disorders
-
Bench, A.J., Nacheva, E.P., Champion, K.M. Green, A.R. (1998) Molecular genetics and cytogenetics of myeloproliferative disorders. Baillière's Clinical Haematology, 11, 819 848.
-
(1998)
Baillière's Clinical Haematology
, vol.11
, pp. 819-848
-
-
Bench, A.J.1
Nacheva, E.P.2
Champion, K.M.3
Green, A.R.4
-
2
-
-
0037229094
-
Mutations in SBDS are associated with Shwachman-Diamond syndrome
-
Boocock, G.R.B., Morrison, J.A., Popovic, M., Richards, N., Ellis, L., Durie, P.R. Rommens, J.M. (2003) Mutations in SBDS are associated with Shwachman-Diamond syndrome. Nature Genetics, 33, 97 101.
-
(2003)
Nature Genetics
, vol.33
, pp. 97-101
-
-
Boocock, G.R.B.1
Morrison, J.A.2
Popovic, M.3
Richards, N.4
Ellis, L.5
Durie, P.R.6
Rommens, J.M.7
-
4
-
-
2942720402
-
Submicroscopic deletions in 5q-associated malignancies
-
Crescenzi, B., La Starza, R., Romoli, S., Beacci, D., Matteucci, C., Barba, G., Aventin, A., Marynen, P., Ciolli, S., Nozzoli, C., Martelli, M.F. Mecucci, C. (2004) Submicroscopic deletions in 5q-associated malignancies. Haematologica, 89, 281 285.
-
(2004)
Haematologica
, vol.89
, pp. 281-285
-
-
Crescenzi, B.1
La Starza, R.2
Romoli, S.3
Beacci, D.4
Matteucci, C.5
Barba, G.6
Aventin, A.7
Marynen, P.8
Ciolli, S.9
Nozzoli, C.10
Martelli, M.F.11
Mecucci, C.12
-
5
-
-
33847222196
-
FIP1L1-PDGFRA in CEL and BCR-ABL1 in CML affect different leukemic cells
-
Crescenzi, B., Chase, A., La Starza, R., Beacci, D., Rosti, V., Gallì, A., Specchia, G., Martelli, M.F., Vandenberghe, P., Cools, J., Jones, A.V., Cross, N.C.P., Marynen, P. Mecucci, C. (2007) FIP1L1-PDGFRA in CEL and BCR-ABL1 in CML affect different leukemic cells. Leukemia, 21, 397 402.
-
(2007)
Leukemia
, vol.21
, pp. 397-402
-
-
Crescenzi, B.1
Chase, A.2
La Starza, R.3
Beacci, D.4
Rosti, V.5
Gallì, A.6
Specchia, G.7
Martelli, M.F.8
Vandenberghe, P.9
Cools, J.10
Jones, A.V.11
Cross, N.C.P.12
Marynen, P.13
Mecucci, C.14
-
6
-
-
18744386071
-
Does isochromosome 7q mandate bone marrow transplant in children with Shwachman-Diamond syndrome?
-
Cunningham, J., Sales, M., Pearce, A., Howard, J., Stallings, R., Telford, N., Wilkie, R., Huntly, B., Thomas, A., O'Marcaigh, A., Will, A. Pratt, N. (2002) Does isochromosome 7q mandate bone marrow transplant in children with Shwachman-Diamond syndrome? British Journal of Haematology, 119, 1062 1069.
-
(2002)
British Journal of Haematology
, vol.119
, pp. 1062-1069
-
-
Cunningham, J.1
Sales, M.2
Pearce, A.3
Howard, J.4
Stallings, R.5
Telford, N.6
Wilkie, R.7
Huntly, B.8
Thomas, A.9
O'Marcaigh, A.10
Will, A.11
Pratt, N.12
-
7
-
-
0036042153
-
Shwachman-Diamond syndrome
-
Dror, Y. (2002) Shwachman-Diamond syndrome. British Journal of Haematology, 118, 701 713.
-
(2002)
British Journal of Haematology
, vol.118
, pp. 701-713
-
-
Dror, Y.1
-
8
-
-
0033230361
-
Shwachman-Diamond syndrome: An inherited preleukemic bone marrow failure disorder with aberrant hematopoietic progenitors and faulty marrow microenviroment
-
Dror, Y. Freedman, M.H. (1999) Shwachman-Diamond syndrome: an inherited preleukemic bone marrow failure disorder with aberrant hematopoietic progenitors and faulty marrow microenviroment. Blood, 94, 3048 3054.
-
(1999)
Blood
, vol.94
, pp. 3048-3054
-
-
Dror, Y.1
Freedman, M.H.2
-
9
-
-
0031702803
-
Malignant myeloid transformation with isochromosome 7q in Shwachman-Diamond syndrome
-
Dror, Y., Squire, J., Durie, P. Freedman, M.H. (1998) Malignant myeloid transformation with isochromosome 7q in Shwachman-Diamond syndrome. Leukemia, 12, 1591 1595.
-
(1998)
Leukemia
, vol.12
, pp. 1591-1595
-
-
Dror, Y.1
Squire, J.2
Durie, P.3
Freedman, M.H.4
-
10
-
-
0036325553
-
Clonal evolution in marrows of patients with Shwachman-Diamond syndrome: A prospective 5-year follow-up study
-
Dror, Y., Durie, P., Ginzberg, H., Herman, R., Banerjee, A., Champagne, M., Shannon, K., Malkin, D. Freedman, M.H. (2002) Clonal evolution in marrows of patients with Shwachman-Diamond syndrome: a prospective 5-year follow-up study. Experimental Hematology, 30, 659 669.
-
(2002)
Experimental Hematology
, vol.30
, pp. 659-669
-
-
Dror, Y.1
Durie, P.2
Ginzberg, H.3
Herman, R.4
Banerjee, A.5
Champagne, M.6
Shannon, K.7
Malkin, D.8
Freedman, M.H.9
-
11
-
-
0030897009
-
International scoring system for evaluation prognosis in myelodysplastic syndromes
-
Greenberg, P., Cox, C., Le Beau, M.M., Fenaux, P., Morel, P., Sanz, G., Sanz, M., Vallespi, T., Hamblin, T., Oscier, D., Ohyashiki, K., Toyama, K., Aul, C., Mufti, G. Bennet, J. (1997) International scoring system for evaluation prognosis in myelodysplastic syndromes. Blood, 89, 2079 2088.
-
(1997)
Blood
, vol.89
, pp. 2079-2088
-
-
Greenberg, P.1
Cox, C.2
Le Beau, M.M.3
Fenaux, P.4
Morel, P.5
Sanz, G.6
Sanz, M.7
Vallespi, T.8
Hamblin, T.9
Oscier, D.10
Ohyashiki, K.11
Toyama, K.12
Aul, C.13
Mufti, G.14
Bennet, J.15
-
12
-
-
0022393713
-
Cytogenetic studies in 174 consecutive patients with preleukemic or myelodysplastic syndromes
-
Knapp, R.H., Dewald, G.W. Pierre, R.V. (1985) Cytogenetic studies in 174 consecutive patients with preleukemic or myelodysplastic syndromes. Mayo Clinic Proceedings, 60, 507 516.
-
(1985)
Mayo Clinic Proceedings
, vol.60
, pp. 507-516
-
-
Knapp, R.H.1
Dewald, G.W.2
Pierre, R.V.3
-
13
-
-
0029929155
-
Haematological abnormalities in Shwachman-Diamond syndrome
-
Smith, O.P., Hann, I.M., Chessells, J.M., Reeves, B.R. Milla, P. (1996) Haematological abnormalities in Shwachman-Diamond syndrome. British Journal of Haematology, 94, 279 284.
-
(1996)
British Journal of Haematology
, vol.94
, pp. 279-284
-
-
Smith, O.P.1
Hann, I.M.2
Chessells, J.M.3
Reeves, B.R.4
Milla, P.5
-
14
-
-
0036786023
-
Intermittent 20q- and consistent i(7q) in a patient with Shwachman-Diamond syndrome
-
Smith, A., Shaw, P.J., Webster, B., Lammi, A., Gaskin, K., Diaz, S. Sharma, P. (2002) Intermittent 20q- and consistent i(7q) in a patient with Shwachman-Diamond syndrome. Pediatric Hematology and Oncology, 19, 525 528.
-
(2002)
Pediatric Hematology and Oncology
, vol.19
, pp. 525-528
-
-
Smith, A.1
Shaw, P.J.2
Webster, B.3
Lammi, A.4
Gaskin, K.5
Diaz, S.6
Sharma, P.7
-
15
-
-
0028295411
-
Deletion of chromosome 20q in myelodysplasia can occur in a multipotent precursor of both myeloid cells and B cells
-
White, N.J., Nacheva, E., Asimakopoulos, F.A., Bloxham, D., Paul, B. Green, A.R. (1994) Deletion of chromosome 20q in myelodysplasia can occur in a multipotent precursor of both myeloid cells and B cells. Blood, 83, 2809 2816.
-
(1994)
Blood
, vol.83
, pp. 2809-2816
-
-
White, N.J.1
Nacheva, E.2
Asimakopoulos, F.A.3
Bloxham, D.4
Paul, B.5
Green, A.R.6
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