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Emilien Petit

Sorbonne Universite
H指数:9
被引数:286

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ATXN8OS Intermediate Expansion Acts as a Genetic Modifier in Spinocerebellar Ataxia Type 48 (SCA48/STUB1)

ATXN8OS 中间扩张在脊髓小脑共济失调48型(SCA48/<i>STUB1</i>)中作为遗传修饰因子发挥作用

2026-09-220
OAAI
Cerebellar cognitive-affective syndrome in Friedreich Ataxia

弗里德赖希共济失调中的小脑认知-情感综合征

2026-06-160
PRE
Value of MRI Outcomes for Preventive and Early-Stage Trials in Spinocerebellar Ataxias 1 and 3

MRI结局在预防性和早期阶段试验中的价值:脊髓小脑共济失调1型和3型

2026-02-100
OAAI
Predictive models for ataxia progression and conversion in spinocerebellar ataxia type 1 and 3

预测脊髓小脑共济失调1型和3型中进展和转化的模型

Brain
IF11.7
2025-10-280
PRE
Longitudinal Changes of Clinical, Imaging, and Fluid Biomarkers in Preataxic and Early Ataxic Spinocerebellar Ataxia Type 2 and 7 Carriers
2024-09-100
OAAI
Sensitivity of Advanced Magnetic Resonance Imaging to Progression over Six Months in Early Spinocerebellar Ataxia

早期脊髓小脑性共济失调的高级磁共振成像对六个月以上进展的敏感性

2024-07-260
OA
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias

非扩张性脊髓小脑共济失调的极端表型异质性

2023-07-0116
OAAI
Baseline Clinical and Blood Biomarker in Patients With Preataxic and Early-Stage Disease Spinocerebellar Ataxia 1 and 3

共济失调和早期疾病脊髓小脑共济失调1和3患者的基线临床和血液生物标志物

2023-04-2512
OA
Intermediate repeat expansions of TBP and STUB1: Genetic modifier or pure digenic inheritance in spinocerebellar ataxias?

TBP和STUB1的中间重复扩增: 脊髓小脑性共济失调中的遗传修饰还是纯的双基因遗传?

2023-02-0119
OAAI
Clinically Meaningful Magnetic Resonance Endpoints Sensitive to Preataxic Spinocerebellar Ataxia Types 1 and 3
2022-12-2922
OAAI