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The number of prognostically detrimental mutations and prognosis in primary myelofibrosis: an international study of 797 patients
2014-01-01 Guglielmelli, P; Lasho, Tl; Rotunno, G; Score, J; Mannarelli, C; Pancrazzi, A; Biamonte, F; Pardanani, A; Zoi, K; Reiter, A; Duncombe, A; Fanelli, T; Pietra, D; Rumi, Elisa; Finke, C; Gangat, N; Ketterling, Rp; Knudson, Ra; Hanson, Ca; Bosi, A; Pereira, A; Manfredini, R; Cervantes, F; Barosi, G; Cazzola, Mario; Cross, Nc; Vannucchi, Am; Tefferi, A.
The origin of serum ferritin in acquired transfusional iron overload in adults. Studies with concanavalin A-sepharose absorption.
1982-01-01 Cazzola, Mario; Bergamaschi, G; Dezza, L; Barosi, G; Ascari, E.
The relevance of transfusion-dependency in the prognostic assessment of patients with myeloid neoplasms
2011-01-01 Malcovati, Luca; Cazzola, Mario
The role of JAK2 mutations in RARS and other MDS.
2008-01-01 Hellström Lindberg, E; Cazzola, Mario
The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts.
2008-01-01 Boultwood, J; Pellagatti, A; Nikpour, M; Pushkaran, B; Fidler, C; Cattan, H; Littlewood, Tj; Malcovati, Luca; DELLA PORTA, MATTEO GIOVANNI; Jädersten, M; Killick, S; Giagounidis, A; Bowen, D; Hellström Lindberg, E; Cazzola, Mario; Wainscoat, Js
The role of the JAK2 GGCC haplotype and the TET2 gene in familial myeloproliferative neoplasms.
2011-01-01 Olcaydu, D; Rumi, Elisa; Harutyunyan, A; Passamonti, F; Pietra, D; Pascutto, C; Berg, T; Jäger, R; Hammond, E; Cazzola, Mario; Kralovics, R.
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy
2021-01-01 Homan, Claire C; King-Smith, Sarah L; Lawrence, David M; Arts, Peer; Feng, Jinghua; Andrews, James; Armstrong, Mark; Ha, Thuong; Dobbins, Julia; Drazer, Michael W; Yu, Kai; Bödör, Csaba; Cantor, Alan; Cazzola, Mario; Degelman, Erin; Dinardo, Courtney D; Duployez, Nicolas; Favier, Remi; Fröhling, Stefan; Fitzgibbon, Jude; Klco, Jeffery M; Krämer, Alwin; Kurokawa, Mineo; Lee, Joanne; Malcovati, Luca; Morgan, Neil V; Natsoulis, Georges; Owen, Carolyn; Patel, Keyur P; Preudhomme, Claude; Raslova, Hana; Rienhoff, Hugh; Ripperger, Tim; Schulte, Rachael; Tawana, Kiran; Velloso, Elvira; Yan, Benedict; Liu, Paul; Godley, Lucy A; Schreiber, Andreas W; Hahn, Christopher N; Scott, Hamish S; Brown, Anna L
The shadowlands of MDS: idiopathic cytopenias of undetermined significance (ICUS) and clonal hematopoiesis of indeterminate potential (CHIP)
2015-01-01 Malcovati, Luca; Cazzola, Mario
The transporter ABCB7 is a mediator of the phenotype of acquired refractory anemia with ring sideroblasts
2013-01-01 Nikpour, M; Scharenberg, C; Liu, A; Conte, S; Karimi, M; Mortera Blanco, T; Giai, V; Fernandez Mercado, M; Papaemmanuil, E; Högstrand, K; Jansson, M; Vedin, I; Stephen Wainscoat, J; Campbell, P; Cazzola, Mario; Boultwood, J; Grandien, A; Hellström Lindberg, E.
The triplicated alpha-gene locus and heterozygous beta thalassaemia: a case of thalassaemia intermedia.
1983-01-01 Sampietro, M; Cazzola, Mario; Cappellini, Md; Fiorelli, G.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| The number of prognostically detrimental mutations and prognosis in primary myelofibrosis: an international study of 797 patients | 1-gen-2014 | Guglielmelli, P; Lasho, Tl; Rotunno, G; Score, J; Mannarelli, C; Pancrazzi, A; Biamonte, F; Pardanani, A; Zoi, K; Reiter, A; Duncombe, A; Fanelli, T; Pietra, D; Rumi, Elisa; Finke, C; Gangat, N; Ketterling, Rp; Knudson, Ra; Hanson, Ca; Bosi, A; Pereira, A; Manfredini, R; Cervantes, F; Barosi, G; Cazzola, Mario; Cross, Nc; Vannucchi, Am; Tefferi, A. | |
| The origin of serum ferritin in acquired transfusional iron overload in adults. Studies with concanavalin A-sepharose absorption. | 1-gen-1982 | Cazzola, Mario; Bergamaschi, G; Dezza, L; Barosi, G; Ascari, E. | |
| The relevance of transfusion-dependency in the prognostic assessment of patients with myeloid neoplasms | 1-gen-2011 | Malcovati, Luca; Cazzola, Mario | |
| The role of JAK2 mutations in RARS and other MDS. | 1-gen-2008 | Hellström Lindberg, E; Cazzola, Mario | |
| The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts. | 1-gen-2008 | Boultwood, J; Pellagatti, A; Nikpour, M; Pushkaran, B; Fidler, C; Cattan, H; Littlewood, Tj; Malcovati, Luca; DELLA PORTA, MATTEO GIOVANNI; Jädersten, M; Killick, S; Giagounidis, A; Bowen, D; Hellström Lindberg, E; Cazzola, Mario; Wainscoat, Js | |
| The role of the JAK2 GGCC haplotype and the TET2 gene in familial myeloproliferative neoplasms. | 1-gen-2011 | Olcaydu, D; Rumi, Elisa; Harutyunyan, A; Passamonti, F; Pietra, D; Pascutto, C; Berg, T; Jäger, R; Hammond, E; Cazzola, Mario; Kralovics, R. | |
| The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy | 1-gen-2021 | Homan, Claire C; King-Smith, Sarah L; Lawrence, David M; Arts, Peer; Feng, Jinghua; Andrews, James; Armstrong, Mark; Ha, Thuong; Dobbins, Julia; Drazer, Michael W; Yu, Kai; Bödör, Csaba; Cantor, Alan; Cazzola, Mario; Degelman, Erin; Dinardo, Courtney D; Duployez, Nicolas; Favier, Remi; Fröhling, Stefan; Fitzgibbon, Jude; Klco, Jeffery M; Krämer, Alwin; Kurokawa, Mineo; Lee, Joanne; Malcovati, Luca; Morgan, Neil V; Natsoulis, Georges; Owen, Carolyn; Patel, Keyur P; Preudhomme, Claude; Raslova, Hana; Rienhoff, Hugh; Ripperger, Tim; Schulte, Rachael; Tawana, Kiran; Velloso, Elvira; Yan, Benedict; Liu, Paul; Godley, Lucy A; Schreiber, Andreas W; Hahn, Christopher N; Scott, Hamish S; Brown, Anna L | |
| The shadowlands of MDS: idiopathic cytopenias of undetermined significance (ICUS) and clonal hematopoiesis of indeterminate potential (CHIP) | 1-gen-2015 | Malcovati, Luca; Cazzola, Mario | |
| The transporter ABCB7 is a mediator of the phenotype of acquired refractory anemia with ring sideroblasts | 1-gen-2013 | Nikpour, M; Scharenberg, C; Liu, A; Conte, S; Karimi, M; Mortera Blanco, T; Giai, V; Fernandez Mercado, M; Papaemmanuil, E; Högstrand, K; Jansson, M; Vedin, I; Stephen Wainscoat, J; Campbell, P; Cazzola, Mario; Boultwood, J; Grandien, A; Hellström Lindberg, E. | |
| The triplicated alpha-gene locus and heterozygous beta thalassaemia: a case of thalassaemia intermedia. | 1-gen-1983 | Sampietro, M; Cazzola, Mario; Cappellini, Md; Fiorelli, G. |
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Opzioni
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Tipologia
- 1 Contributo su Rivista 483
- 1 Contributo su Rivista::1.1 Arti... 469
- 1 Contributo su Rivista::1.5 Abst... 14
Data di pubblicazione
- 2020 - 2024 26
- 2010 - 2019 170
- 2000 - 2009 127
- 1990 - 1999 77
- 1980 - 1989 73
- 1974 - 1979 10
Editore
- Macmillan Magazines Limited:Porte... 4
- Blackwell Science Limited:PO Box ... 3
- American Society of Hematology:19... 2
- American Society for Biochemistry... 1
- Elsevier Science Incorporated / N... 1
- John Wiley & Sons Incorporated:Cu... 1
- Marcel Dekker Incorporated:270 Ma... 1
Rivista
- HAEMATOLOGICA 103
- BLOOD 96
- BRITISH JOURNAL OF HAEMATOLOGY 54
- LEUKEMIA 35
- AMERICAN JOURNAL OF HEMATOLOGY 17
- AMERICAN JOURNAL OF HEMATOLOGY 11
- JOURNAL OF CLINICAL ONCOLOGY 10
- SCANDINAVIAN JOURNAL OF HAEMATOLOGY 9
- THE NEW ENGLAND JOURNAL OF MEDICINE 9
- BLOOD 6
Keyword
- Myelodysplastic syndrome 60
- Anemia 45
- Iron 31
- Myeloproliferative neoplasm 28
- JAK2 22
- prognosis 19
- Erythropoietin 18
- Erythropoiesis 17
- mutation 17
- MYELODYSPLASTIC SYNDROME 17
Lingua
- eng 477
- ita 2
- spa 1
Accesso al fulltext
- no fulltext 483