Motor unit number index: A potential electrophysiological biomarker for pediatric spinal muscular atrophy-Reference-Cited by-同舟云学术

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Motor unit number index: A potential electrophysiological biomarker for pediatric spinal muscular atrophy

Published:2021-09 Issue:4 Volume:64 Page:445-453
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle & Nerve

Author:

Boulay Christophe¹²³,Delmont Emilien²⁴,Audic Frédérique¹²,Chabrol Brigitte¹²⁵,Attarian Shahram²⁵

Affiliation:

1. Neuropediatric Department Children Timone University Hospital, Aix‐Marseille University Marseille France

2. Reference Center for Neuromuscular Diseases and ALS Timone University Hospital Aix‐Marseille University Marseille France

3. Aix‐Marseille University, CNRS, ISM UMR 7287 Marseille France

4. Aix‐Marseille University, UMR 7286, Medicine Faculty Marseille France

5. Aix‐Marseille University, Inserm UMR S 910, Medical Genetics and Functional Genomics Marseille France

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.27372

Reference59 articles.

1. Identification and characterization of a spinal muscular atrophy-determining gene

2. Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care

3. 209th ENMC International Workshop: Outcome Measures and Clinical Trial Readiness in Spinal Muscular Atrophy 7–9 November 2014, Heemskerk, The Netherlands

4. Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy

5. Longitudinal characterization of biomarkers for spinal muscular atrophy

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1. Could the motor unit number index be an early prognostic biomarker for amyotrophic lateral sclerosis?;Clinical Neurophysiology;2024-07

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3. Neurophysiological Characteristics in Type II and Type III 5q Spinal Muscular Atrophy Patients: Impact of Nusinersen Treatment;Drug Design, Development and Therapy;2024-03

4. Correlations between clinical motor scores and CMAP in patients with type 2 spinal muscular amyotrophy treated with nusinersen;Archives de Pédiatrie;2024-01

5. Long‐term follow‐up of 64 children with classical infantile‐onset Pompe disease since 2004: A French real‐life observational study;European Journal of Neurology;2023-06-10

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