arrow
M

Mario Cazzola

University of Pavia
H指数:117
被引数:7.7万

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Defining remission and relapse after allogeneic hematopoietic cell transplantation in myelodysplastic/myeloproliferative neoplasms and optimization of transplantation outcomes: Recommendations from the EBMT practice harmonisation and guidelines committee

定义异基因造血细胞移植后骨髓增生异常/骨髓增生性肿瘤的缓解和复发,并优化移植结果:EBMT实践协调与指南委员会的建议

2026-04-010
PRE
A Precision Medicine Approach to the Myelodysplastic Syndrome with Isolated Deletion 5q, Fifty Years After Its Discovery

孤立性5q缺失骨髓增生异常综合征的精准医学研究进展——发现五十周年纪念

Blood
IF23.1
2025-08-060
PRE
A precision medicine approach to the myelodysplastic syndrome with isolated deletion 5q, 50 years after its discovery

孤立性5q缺失骨髓增生异常综合征的精准医学研究,自其发现以来的50年

Blood
IF23.1
2025-08-060
PRE
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41
2023-10-1213
OAAI
Implementation and adoption of a web tool to support precision diagnostic and treatment decisions for patient with myelodysplastic syndromes

实施和采用网络工具以支持骨髓增生异常综合征患者的精确诊断和治疗决策

2023-04-040
PRE
Pseudouridine-modified tRNA fragments repress aberrant protein synthesis and predict leukaemic progression in myelodysplastic syndrome

假尿苷修饰的tRNA片段抑制异常蛋白质合成并预测骨髓增生异常综合征的白血病进展

2022-03-1563
OAAI
PD-L1 overexpression correlates with JAK2-V617F mutational burden and is associated with 9p uniparental disomy in myeloproliferative neoplasms
2022-01-2114
OAAI
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
2021-07-0832
OAAI
Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes (vol 26, pg 1549, 2020)

TP53等位基因状态对骨髓增生异常综合征基因组稳定性、临床表现和预后的影响 (第26卷,1549页,2020)

2021-05-045
OAAI
Gene expression profile correlates with molecular and clinical features in patients with myelofibrosis
2021-03-0510
OA
Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes (vol 26, pg 1549, 2020)

TP53等位基因状态对骨髓增生异常综合征基因组稳定性、临床表现和预后的影响 (第26卷,1549页,2020)

2021-02-092
OAAI
Co-mutation pattern, clonal hierarchy, and clone size concur to determine disease phenotype of SRSF2P95-mutated neoplasms
LEUKEMIA
IF13.4
2020-12-2120
PREAI
Implications ofTP53allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes

Tp53等位基因状态对骨髓增生异常综合征基因组稳定性、临床表现和预后的影响

2020-08-03406
OAAI