CSF Proteomic Profiling Reveals Altered Pathways in Myotonic Dystrophy Type 1 (P2-11.029)

To identify myotonic dystrophy type 1 (DM1) biomarkers through a comprehensive proteomic evaluation of cerebrospinal fluid (CSF) from patients.

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Publication Details

Journal
Neurology
Published
2025-04-07
DOI
https://doi.org/10.1212/wnl.0000000000211981
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.00
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article

CSF Proteomic Profiling Reveals Altered Pathways in Myotonic Dystrophy Type 1 (P2-11.029)

Jacinda B. Sampson, Katharine A. Hagerman, John Day, Tahereh Kamali et al.
Neurology
Genetic Neurodegenerative Diseases
article

CSF Proteomic Profiling Reveals Altered Pathways in Myotonic Dystrophy Type 1 (P2-11.029)

Jacinda B. Sampson, Katharine A. Hagerman, John Day, Tahereh Kamali, Marwa Zafarullah, Lisa Ghiglieri
article en

Abstract

To identify myotonic dystrophy type 1 (DM1) biomarkers through a comprehensive proteomic evaluation of cerebrospinal fluid (CSF) from patients.

NeurologyVol. 104(7_Supplement_1)
Stanford University (US)
Openalex Percentile: Top 92%
Genetic Neurodegenerative Diseases
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