Results 111 to 120 of about 54,906 (291)
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To determine whether myelin‐sensitive quantitative MRI reveals microstructural abnormalities in normal‐appearing cortex (NACtx) in myelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD), indicating that conventional MRI underestimates remission residual cortical injury.
Valentina Camera +20 more
wiley +1 more source
On the Uniqueness of the Standard Genetic Code
Life, 2017 In this work, we determine the biological and mathematical properties that are sufficient and necessary to uniquely determine both the primeval RNY (purine-any base-pyrimidine) code and the standard genetic code (SGC). These properties are: the evolution
Gabriel S. Zamudio, Marco V. José
doaj +1 more source
Monthly Notices of the Royal Astronomical Society, 1935 Moller, Chr., Chandrasekhar, S.
openaire +2 more sources
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To investigate which baseline clinical and imaging characteristics best predict TSPO‐PET‐measurable reduction in glial activation following treatment of multiple sclerosis (MS), to utilize this information for designing more efficient biomarker‐based clinical trials targeting glial activation.
Marlene T. Morch +5 more
wiley +1 more source
The declination degeneracy in interferometric astrometry
, 2012 Context. Interferometric astrometry at radio and optical wavelengths serves as a fundamental and high-precision method for measuring the positions of celestial objects and for geodetic and Earth orientation measurements. Aims. We determine the
D. Buscher
core +1 more source
Exact Solutions and Degenerate Properties of Spin Chains with Reducible Hamiltonians
Condensed Matter, 2018 The Jordan–Wigner transformation plays an important role in spin models. However, the non-locality of the transformation implies that a periodic chain of N spins is not mapped to a periodic or an anti-periodic chain of lattice fermions.
Shiung Fan
doaj +1 more source
Global Rather Than Vertical‐Selective Saccadic Abnormalities in Progressive Supranuclear Palsy
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To test whether vertical saccades are preferentially affected in Progressive Supranuclear Palsy (PSP). Methods PSP patients (n = 24) were compared to age‐matched controls (n = 94) and two degenerative groups (Alzheimer's disease, n = 20; Lewy body disease, n = 50).
Duy Duan Nguyen +6 more
wiley +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background Hereditary Spastic Paraplegia (HSP) comprises a group of rare genetic diseases characterized by length‐dependent axonal degeneration of the corticospinal tracts and dorsal columns, whose main clinical feature is spastic gait. Pathogenic variants in the SPG4 gene cause Spastic Paraplegia Type 4 (SPG4‐HSP), the most common form of HSP.
Gaia Fattorini +12 more
wiley +1 more source
Positive Fitted Finite Volume Method for Semilinear Parabolic Systems on Unbounded Domain
AxiomsThis work deals with a semilinear system of parabolic partial differential equations (PDEs) on an unbounded domain, related to environmental pollution modeling.
Miglena N. Koleva, Lubin G. Vulkov
doaj +1 more source
Progressive Parkinsonism in PPP2R5D‐Related Neurodevelopmental Disorder
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT PPP2R5D‐related neurodevelopmental disorder (Houge–Janssens syndrome type 1) is a rare autosomal dominant condition characterized by macrocephaly, intellectual disability, and epilepsy. Progressive parkinsonism is an emerging adult phenotype that neurologists should be aware of since timely genetic diagnosis opens the door to disease‐modifying
Katerina Bernardi +6 more
wiley +1 more source