Results 81 to 90 of about 7,905,524 (289)

The Role of Calcitonin Gene‐Related Peptide in High‐Altitude Headache: A Prospective Field Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective High‐altitude headache (HAH) is a common neurological condition associated with rapid ascent to high altitude. The pathophysiological mechanisms underlying HAH remain incompletely understood. Calcitonin gene‐related peptide (CGRP), a neuropeptide implicated in migraine pathophysiology, may play a key role in the pathophysiology of ...
Roman Schniepp   +4 more
wiley   +1 more source

Kazakistan-Türkiye İlişkilerinin Gelişiminde Akıllı Güç

open access: yesİmgelem
Bu çalışmada Kazakistan-Türkiye ilişkilerinin gelişimine etki eden faktörlerin neler olduğu incelenmektedir. Günümüzdeki Kazakistan-Türkiye ilişkilerinin çok boyutlu olduğu ve ne yumuşak ne de sert güç perspektifinden iki ülke ilişkilerini irdelemenin ...
Erol Kalkan, Madina Bektassova
doaj   +1 more source

SOFT POWER: THE CONCEPT AND APPROACHES

open access: yesVestnik MGIMO-Universiteta, 2017
The article examines the correlation of two concepts: «soft power» and «propaganda» in International Relations. The author argues that within realism these concepts are used synonymously, but within neoliberalism they have fundamental differences.
M. M. Lebedeva
doaj   +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

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

Turkey’s Military Role in Libya and Its Wider Strategic Environment (interest) in the Eastern Mediterranean Basin

open access: yesJournal of Central and Eastern European African Studies
As a result of the Arab Spring and the return to building the sphere of interest of the Ottoman past, Turkey’s relations with the countries of the North African region are increasingly appreciating, and they seem to be a longer-term vision in Turkish ...
András Málnássy
doaj   +1 more source

Dementia Incidence in Individuals With Parkinson's Disease in the Framingham Heart Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Limited information exists on incident dementia in individuals with Parkinson's disease (PD) in US community‐based samples. We examined cognitive statuses and PD diagnoses of 183 individuals in the Framingham Heart Study (FHS) to establish incident dementia, mortality rates, associations with sex, age at PD onset, and education level.
Joshi Dookhy   +11 more
wiley   +1 more source

Russian Fear Management: Between Hard and Soft Power in the Near Abroad – The Case of Poland

open access: yesPolish Political Science Yearbook
This article critically examines the Russian Federation’s international influence strategies, particularly toward Poland, through the lens of soft and hard power theory.
Monika Mazur-Bubak
doaj   +1 more source

Prognostic Value of Neurofilament Light Chain and Glial Fibrillary Acidic Protein in ALD‐Related Myelopathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background X‐linked adrenoleukodystrophy (X‐ALD) is a neurometabolic disorder caused by pathogenic variants in ABCD1, leading to slowly progressive spinal cord disease in nearly all affected men. Sensitive biomarkers to quantify disease severity and predict progression are needed for clinical care and trial design.
Eda G. Kabak   +4 more
wiley   +1 more source

Memory and Resting‐State Connectivity in Acute Transient Global Amnesia: A Case–Control fMRI Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Transient global amnesia (TGA) is a striking model of isolated amnesia. While hippocampal lesions are well described, the network‐level mechanisms and the precise neuropsychological profile remain debated. Our objective was thus to characterize functional and neuropsychological correlates of acute TGA and their ...
Elias El Otmani   +10 more
wiley   +1 more source

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