Louis Viollet
Overview
Explore the profile of Louis Viollet including associated specialties, affiliations and a list of published articles.
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23
Citations
642
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Recent Articles
1.
Shulman M, Kong J, OGorman J, Ratti E, Rajagovindan R, Viollet L, et al.
Nat Aging
. 2023 Nov;
3(12):1591-1601.
PMID: 38012285
In Alzheimer's disease, the spread of aberrantly phosphorylated tau is an important criterion in the Braak staging of disease severity and correlates with disease symptomatology. Here, we report the results...
2.
Rosewich H, Sweney M, DeBrosse S, Ess K, Ozelius L, Andermann E, et al.
Neurol Genet
. 2017 Mar;
3(2):e139.
PMID: 28293679
Objective: -related neurologic disorders encompass a broad range of phenotypes that extend well beyond initial phenotypic criteria associated with alternating hemiplegia of childhood (AHC) and rapid-onset dystonia parkinsonism. Methods: In...
3.
Catteruccia M, Vuillerot C, Vaugier I, Leclair D, Azzi V, Viollet L, et al.
J Neuromuscul Dis
. 2016 Nov;
2(4):453-462.
PMID: 27858747
Background: Scoliosis is the most debilitating issue in SMA type 2 patients. No evidence confirms the efficacy of Garches braces (GB) to delay definitive spinal fusion. Objective: Compare orthopedic and...
4.
Viollet L, Glusman G, Murphy K, Newcomb T, Reyna S, Sweney M, et al.
PLoS One
. 2015 Sep;
10(8):e0137370.
PMID: 26322789
No abstract available.
5.
Viollet L, Glusman G, Murphy K, Newcomb T, Reyna S, Sweney M, et al.
PLoS One
. 2015 May;
10(5):e0127045.
PMID: 25996915
Mutations in ATP1A3 cause Alternating Hemiplegia of Childhood (AHC) by disrupting function of the neuronal Na+/K+ ATPase. Published studies to date indicate 2 recurrent mutations, D801N and E815K, and a...
6.
Lewelt A, Krosschell K, Stoddard G, Weng C, Xue M, Marcus R, et al.
Muscle Nerve
. 2015 Jan;
52(4):559-67.
PMID: 25597614
Introduction: Preliminary evidence in adults with spinal muscular atrophy (SMA) and in SMA animal models suggests exercise has potential benefits in improving or stabilizing muscle strength and motor function. Methods:...
7.
Viollet L, Melki J
Handb Clin Neurol
. 2013 Apr;
113:1395-411.
PMID: 23622363
Spinal muscular atrophies (SMA) are genetic disorders characterized by degeneration of lower motor neurons. The most frequent form is caused by mutations of the survival motor neuron 1 gene (SMN1)....
8.
Heinzen E, Swoboda K, Hitomi Y, Gurrieri F, Nicole S, de Vries B, et al.
Nat Genet
. 2012 Jul;
44(9):1030-4.
PMID: 22842232
Alternating hemiplegia of childhood (AHC) is a rare, severe neurodevelopmental syndrome characterized by recurrent hemiplegic episodes and distinct neurological manifestations. AHC is usually a sporadic disorder and has unknown etiology....
9.
Blumen S, Astord S, Robin V, Vignaud L, Toumi N, Cieslik A, et al.
Ann Neurol
. 2012 Apr;
71(4):509-19.
PMID: 22522442
Objective: Distal hereditary motor neuropathies (dHMN) form a clinically and genetically heterogeneous group of disorders, characterized by muscle weakness and atrophy predominating at the distal part of the limbs, due...
10.
Michot C, Hubert L, Romero N, Gouda A, Mamoune A, Mathew S, et al.
J Inherit Metab Dis
. 2012 Apr;
35(6):1119-28.
PMID: 22481384
Background: Recessive LPIN1 mutations were identified as a cause of severe rhabdomyolysis in pediatric patients. The human lipin family includes two other closely related members, lipin-2 and 3, which share...