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Richard G. Grundy

University of Nottingham
H指数:63
被引数:1.5万

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THE MANAGEMENT OF PEDIATRIC AND ADOLESCENT SPINAL EPENDYMOMA; A 20-YEAR NATIONAL EVALUATION INVOLVING UNITED KINGDOM PEDIATRIC ONCOLOGY PRIMARY TREATMENT CENTERS ON BEHALF OF THE UK CHILDREN'S CANCER AND LEUKAEMIA GROUP (CCLG)
2024-06-180
OAAI
Metabolite profiles of medulloblastoma for rapid and non-invasive detection of molecular disease groups

髓母细胞瘤的代谢物谱,用于分子疾病组的快速和无创检测

2024-02-012
OAAI
OPTIMISING BIOMARKERS FOR ACCURATE EPENDYMOMA DIAGNOSIS, PROGNOSTICATION AND STRATIFICATION WITHIN INTERNATIONAL CLINICAL TRIALS: A BIOMECA STUDY
2023-06-121
OAAI
A MULTICENTER STUDY OF POOR PROGNOSIS CHROMOSOME 1Q GAIN AND/OR 6Q LOSS IN POSTERIOR FOSSA A EPENDYMOMA SHOWS INCREASED PREVALENCE FROM 20% AT DIAGNOSIS TO 60% AT FIRST RECURRENCE
2023-06-120
OAAI
Significant increase of high-risk chromosome 1q gain and 6q loss at recurrence in posterior fossa group A ependymoma: A multicenter study

后颅窝A组室管膜瘤复发时高危染色体1q增加和6q丢失显著增加: 一项多中心研究

2023-05-295
OA
Lineage switching of the cellular distribution of BRAFV600E in multisystem Langerhans cell histiocytosis
2023-05-157
OAAI
Pediatric-type high-grade neuroepithelial tumors with CIC gene fusion share a common DNA methylation signature

具有CIC基因融合的儿科型高级别神经上皮肿瘤具有共同的DNA甲基化特征

2023-03-248
OAAI
Optimizing biomarkers for accurate ependymoma diagnosis, prognostication, and stratification within International Clinical Trials: A BIOMECA study
2023-03-142
OAAI
Recurrent posterior fossa group A (PFA) ependymoma in a young child with constitutional mismatch repair deficiency (CMMRD)

患有宪法错配修复缺陷 (CMMRD) 的幼儿复发性后颅窝A组 (PFA) 室管膜瘤

2022-11-186
OAAI
Recurrent ACVR1 mutations in posterior fossa ependymoma

后颅窝室管膜瘤的复发性ACVR1突变

2022-05-198
OA