Results 41 to 50 of about 249,622 (267)

Lower-Dimensional Model of the Flow and Transport Processes in Thin Domains by Numerical Averaging Technique

open access: yesFluids, 2023
In this work, we present a lower-dimensional model for flow and transport problems in thin domains with rough walls. The full-order model is given for a fully resolved geometry, wherein we consider Stokes flow and a time-dependent diffusion–convection ...
Maria Vasilyeva   +2 more
doaj   +1 more source

"THE CORPUS LUTEUM.' [PDF]

open access: yesThe Lancet, 1886
n ...
openaire   +1 more source

SPG4 and Dementia: Expanding the Clinical Spectrum

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza   +19 more
wiley   +1 more source

¿COMO NUESTROS PADRES HAN CREÍDO? JÓVENES EVANGÉLICOS Y DESAFILIACIÓN ECLESIAL EN MÉXICO

open access: yesRevista Cultura & Religión, 2014
Recientemente los estudios que articulan el fenómeno juvenil con el religioso han tenido que plantearse la problemática de la distancia creciente que tienen los jóvenes con las instancias religiosas convencionales.
Ariel Corpus
doaj  

ON CORPUS LINGUISTICS AND THE NATIONAL CORPUS

open access: yes, 2023
In this article, the formation and development of corpus linguistics, the main concepts and issues, the creation of corpora, the requirements for the formation of the linguistic base of corpora, the educational corpus of the Uzbek language, the stages of development of corpus linguistics, the contributions of our scientists to corpus linguistics, the ...
Abduvohidov, Behruz, Abdualimova, G.H.
openaire   +1 more source

Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone   +8 more
wiley   +1 more source

Understanding Further the Phenotypic Spectrum of Central Nervous System Inflammatory Demyelinating Disorders Using Unsupervised Clustering

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Central nervous system (CNS) inflammatory demyelinating syndromes, including multiple sclerosis (MS), aquaporin‐4 antibody–positive neuromyelitis optica spectrum disorder (AQP4 + NMOSD), and myelin oligodendrocyte glycoprotein (MOG) antibody–associated disease (MOGAD), occasionally overlap.
Bade Gulec   +6 more
wiley   +1 more source

Empowering criminal justice majors: developing communication skills for a post-COVID era

open access: yesHumanities & Social Sciences Communications
This study explores integrating virtual reality (VR) simulations and applied improvisational theater techniques into criminal justice education to address evolving communication challenges, particularly in the wake of the COVID-19 pandemic. Grounded in a
Callie Shaw   +4 more
doaj   +1 more source

Influence of Loop Current and eddy shedding on subseasonal sea level variability along the western Gulf Coast

open access: yesFrontiers in Marine Science, 2023
Mechanisms that generate subseasonal (1-2 months) events of sea level rise along the western Gulf Coast are investigated using the data collected by a dense tide gauge network: Texas Coastal Ocean Observation Network (TCOON) and National Water Level ...
Toshiaki Shinoda   +2 more
doaj   +1 more source

Movement Disorders in Aicardi–Goutières Syndrome and Response to Immunomodulation

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT This study characterizes movement disorders and treatment responses in seven children with Aicardi–Goutières syndrome (AGS). We retrospectively evaluated motor phenotypes, neuroimaging, and interferon signatures in patients treated with baricitinib or anifrolumab. Spasticity affected all patients, while dystonia was present in 4/7.
Enrique Gonzalez Saez‐Diez   +10 more
wiley   +1 more source

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