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Patrick R. Benusiglio

pitie-salpetriere hospital
H指数:24
被引数:3,492

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Gliomas with pleomorphic and pseudopapillary features (GPAP) are circumscribed tumors with targetable mutations, prolonged survival, and frequent tumor predisposition

具有多形性和假乳头状特征的胶质瘤(GPAP)是边界清晰的肿瘤,具有可靶向的突变、生存期延长和频繁的肿瘤易感性

2026-09-300
OAAI
Correction: follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: data from the PRED-IdF network

更正:随访、癌症风险和Peutz-Jeghers综合征的死亡率:来自PRED-IdF网络的数据

2026-07-030
OA
Follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: Data from the PRED-IdF network

Peutz-Jeghers综合征的随访、癌症风险和死亡率:PRED-IdF网络的数据

2026-05-130
OAAI
French recommendations on multi-gene panel testing in renal cell carcinoma

法国关于肾细胞癌多基因 panel 检测的建议

2025-11-010
OAAI
A Specific Methylation Class Identifies BAP1-Deficient Meningiomas, Including Meningeal Tumours With Poorly Differentiated Nonrhabdoid Histology

一种特定的甲基化类别可识别BAP1缺陷型脑膜瘤,包括具有未分化非横纹样组织学的脑膜肿瘤。

2025-09-300
OAAI
The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)

PTEN错构瘤综合征(PHTS)中第二原发癌的风险

2025-05-240
OAAI
Features of colorectal adenomas among young patients with Lynch syndrome according to path_MMR: Results from the PRED-IdF registry
2024-04-011
PRE
Prediction of response to immune checkpoint blockade in patients with metastatic colorectal cancer with microsatellite instability
2023-08-0112
OA
Lynch syndrome: influence of additional susceptibility variants on cancer risk
2023-04-243
OA
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer

AXIN2种系在法国队列中的测试证实了致病变异是结直肠息肉病和癌症易感性的罕见原因

2022-12-214
OAAI
Cancer risks by sex and variant type in PTEN hamartoma tumor syndrome
2022-09-2818
OA
First estimates of diffuse gastric cancer risks for carriers of CTNNA1 germline pathogenic variants

首次估计CTNNA1种系致病变异携带者的弥漫性胃癌风险

2022-08-2912
PRE
Management of Pathogenic CDH1 Variant Carriers Within the FREGAT Network A Multicentric Retrospective Study
2022-07-201
PRE
Cancer risk and tumour spectrum in 172 patients with a germline SUFU pathogenic variation: a collaborative study of the SIOPE Host Genome Working Group
2022-06-298
OAAI