Unilateral problems for the Klein-Gordon operator with nonlinearity of Kirchhoff-Carrier type
Electronic Journal of Differential Equations, 2015 This work concerns the unilateral problem for the Klein-Gordon operator $$ \mathbb{L}=\frac{\partial^2 u}{\partial t^2}-M(|\nabla u|^2)\Delta u+M_1(|u|^2)u-f.
Carlos Raposo +3 more
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Shadow Analysis of an Approximate Rotating Black Hole Solution with Weakly Coupled Global Monopole Charge [PDF]
Mohsen Fathi
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Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Amyotrophic lateral sclerosis (ALS) is a neuromuscular disease. Super oxide dismutase 1 (SOD1) gene mutations cause ALS, and the D90A mutation is associated with primarily upper motor neuron (UMN) loss. Objective Our goal is to reveal the early cellular events in ALS pathology and identify potential pharmacokinetic biomarkers, using well ...
Mukesh Gautam +6 more
wiley +1 more source
Weighted $W^{1,p}$- estimates for weak solutions of degenerate elliptic\n equations with coefficients degenerate in one variable [PDF]
, 2016 Tadele Mengesha, Tuoc Phan
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini +13 more
wiley +1 more source
A global weak solution to the full bosonic string heat flow
, 2017 Volker Branding
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Nonuniqueness of weak solutions of the nonlinear Schroedinger equation [PDF]
, 2005 Michael Christ
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SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas +18 more
wiley +1 more source
Higher derivatives of suitable weak solutions of the hypodissipative Navier-Stokes equations [PDF]
, 2020 Hyunju Kwon, Wojciech S. Ożański
openalex
Relapsing–Remitting Multiple Sclerosis Is Associated With a Dysbiotic Oral Microbiome
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Multiple sclerosis (MS) is a chronic autoimmune disorder characterized by inflammation, demyelination, and neurological impairment. While the gut microbiota's role in MS is extensively studied, the association between the oral microbiota and MS remains underexplored, particularly in North American cohorts.
Sukirth M. Ganesan +12 more
wiley +1 more source