Unconditional flocking for weak solutions to self-organized systems of Euler-type with all-to-all interaction kernel [PDF]
, 2023 Debora Amadori, Cleopatra Christoforou
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Cognitive impairment, fatigue, and depression are common in multiple sclerosis (MS), potentially due to disruption of regional functional connectivity caused by white matter (WM) lesions. We explored whether WM lesions functionally connected to specific brain regions contribute to these MS‐related manifestations.
Alessandro Franceschini +7 more
wiley +1 more source
Besov Regularity of Weak solutions to a Class of Nonlinear Elliptic Equations [PDF]
Huimin Cheng, Xuechang Zhou
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Very weak solutions of the Navier-Stokes equations in exterior domains with nonhomogeneous data [PDF]
, 2007 Reinhard Farwig +2 more
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A remark on weak-strong uniqueness for suitable weak solutions of the Navier–Stokes equations
, 2022 Pierre Gilles Lemarié–Rieusset
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Weak solutions of non-isothermal nematic liquid crystal flow in dimension three [PDF]
, 2020 Hengrong Du, Yimei Li, Changyou Wang
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Existence of a weak solution to a regularized moving boundary fluid-structure interaction problem with poroelastic media [PDF]
, 2023 Jeffrey Kuan +2 more
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INF2‐Related Charcot–Marie–Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background INF2 mutations cause focal segmental glomerulosclerosis (FSGS) and Charcot–Marie–Tooth disease (CMT). Accurate genetic diagnosis is critical, as INF2‐related FSGS is typically resistant to immunotherapy yet rarely recurs after transplantation, and its associated neuropathy can mimic treatable immune‐mediated disorders such as ...
Chikashi Yano +27 more
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Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco +18 more
wiley +1 more source