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David Sumerauer

Charles University and Motol University Hospital
H指数:28
被引数:4,818

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Pediatric ependymoma in the molecular era: real-world experience with diagnostic correlation and long-term clinical outcomes

儿科室管膜瘤在分子时代:与诊断相关的真实世界经验及长期临床结果

2026-08-050
OA
Molecular Landscape of Pediatric Low-Grade Gliomas: Insights From RNA-NGS and Bioinformatic Analysis

儿童低级别胶质瘤的分子景观:来自RNA-NGS和生物信息学分析的见解

2025-10-110
OAAI
Diffuse pediatric high-grade glioma of methylation-based RTK2A and RTK2B subclasses present distinct radiological and histomolecular features including Gliomatosis cerebri phenotype
2024-11-180
OAAI
AGE ABOVE 12 MONTHS, ABSENCE OF SYNCHRONOUS, MULTIFOCAL DISEASE AND PATHOGENIC GERMLINE VARIANTS AT C-TERMINI ARE POSITIVE PROGNOSTIC FACTORS IN CHILDREN WITH RTPS1 (RHABDOID-TUMOR-PREDISPOSITION-SYNDROME)
2024-06-180
OAAI
PEDIATRIC-TYPE DIFFUSE HIGH-GRADE GLIOMA OF METHYLATION-BASED RTK2A AND RTK2B SUBCLASSES PRESENT DISTINCT RADIOLOGICAL AND HISTOMOLECULAR FEATURES
2024-06-180
OAAI
Clinical and molecular study of radiation-induced gliomas
2024-02-072
OAAI
A multi-institutional retrospective pooled outcome analysis of molecularly annotated pediatric supratentorial ZFTA-fused ependymoma

分子标记的小儿幕上ZFTA融合室管膜瘤的多机构回顾性汇总结果分析

2023-05-126
OAAI
Integrated genomic analysis reveals actionable targets in pediatric spinal cord low-grade gliomas (vol 10, 143, 2022)
2022-11-110
OAAI
Integrated genomic analysis reveals actionable targets in pediatric spinal cord low-grade gliomas

整合基因组分析揭示了小儿脊髓低级别胶质瘤的可行靶点

2022-09-266
OAAI
ATRT-SHH comprises three molecular subgroups with characteristic clinical and histopathological features and prognostic significance
2022-04-3027
OAAI
Genomic predictors of response to PD-1 inhibition in children with germline DNA replication repair deficiency

生殖系DNA复制修复缺陷儿童对PD-1抑制反应的基因组预测因子

2022-01-0672
OAAI
Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B
2021-09-2026
OAAI
PATZ1 fusions define a novel molecularly distinct neuroepithelial tumor entity with a broad histological spectrum

PATZ1融合定义了一种具有广泛组织学谱的新型分子独特的神经上皮肿瘤实体

2021-08-2138
OAAI
Therapeutic implications of improved molecular diagnostics for rare CNS embryonal tumor entities: results of an international, retrospective study

改进分子诊断对罕见中枢神经系统胚胎性肿瘤实体的治疗意义: 一项国际回顾性研究的结果

2021-06-0223
OA
Pattern of Relapse and Treatment Response in WNT-Activated Medulloblastoma
2020-06-0125
OAAI