Suchergebnisse - "Petit, Emilien"

PubPharm (7)

1

Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias

enthalten in: American journal of human genetics | 2023

von Cunha, P. | Petit, E. | Coutelier, M. | +69

2

Baseline Clinical and Blood Biomarkers in Patients With Preataxic and Early-Stage Disease Spinocerebellar Ataxia 1 and 3

enthalten in: Neurology | 2023

von Tezenas du Montcel, S. | Petit, E. | Olubajo, T. | +13

3

Clinically Meaningful Magnetic Resonance Endpoints Sensitive to Preataxic Spinocerebellar Ataxia Types 1 and 3

enthalten in: Annals of neurology | 2023

von Chandrasekaran, J. | Petit, E. | Park, Y. | +56

4

Intermediate repeat expansions of TBP and STUB1 : Genetic modifier or pure digenic inheritance in spinocerebellar ataxias?

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2023

von Barbier, M. | Davoine, C. | Petit, E. | +19

5

Temporal Dynamics of the Scale for the Assessment and Rating of Ataxia in Spinocerebellar Ataxias

enthalten in: Movement disorders : official journal of the Movement Disorder Society | 2023

von Moulaire, P. | Poulet, P. | Petit, E. | +5

6

Clinically Meaningful Magnetic Resonance Endpoints Sensitive to Preataxic Spinocerebellar Ataxia Types1 and3

enthalten in: Annals of Neurology | 2023

von Chandrasekaran, J. | Petit, E. | Park, Y. | +22

7

Plasma neurofilament light chain predicts cerebellar atrophy and clinical progression in spinocerebellar ataxia

enthalten in: Neurobiology of disease | 2021

von Coarelli, G. | Darios, F. | Petit, E. | +6

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