Results 101 to 110 of about 207,274 (314)

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

Semantically-Guided Image Compression for Enhanced Perceptual Quality at Extremely Low Bitrates

open access: yesIEEE Access
Image compression methods based on machine learning have achieved high rate-distortion performance. However, the reconstructions they produce suffer from blurring at extremely low bitrates (below 0.1 bpp), resulting in low perceptual quality.
Shoma Iwai   +2 more
doaj   +1 more source

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

Embodied Image Compression

open access: yesCoRR
15 pages, 12 figures, 3 ...
Chunyi Li   +8 more
openaire   +2 more sources

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

A generic postprocessing technique for image compression

open access: yes, 2001
A postprocessing approach is developed for image coding applications. In this approach, a distortion-recovery model extracts multi-resolution edge features from the decompressed image and uses these visual features as input to estimate the difference ...
He, Z., Luk, B. L., Chen, S.
core  

Low complexity video compression using moving edge detection based on DCT coefficients [PDF]

open access: yes, 2009
In this paper, we propose a new low complexity video compression method based on detecting blocks containing moving edges us- ing only DCT coe±cients.
Kim, Chanyul   +4 more
core   +1 more source

Ofatumumab in Myelin Oligodendrocyte Glycoprotein Antibody–Associated Disease: A Comparison With Rituximab

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To evaluate the efficacy and safety of ofatumumab in patients with myelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD), and compare it with rituximab. Methods We conducted a single–center, observational study including 22 MOGAD patients treated with ofatumumab and 21 treated with rituximab.
Yuxin Fan   +5 more
wiley   +1 more source

Image compression encryption and reversible destruction algorithm based on chaotic sequence or periodic sequence

open access: yesAin Shams Engineering Journal
Aiming at the problem that it is difficult to realize the coexistence of encryption and compression for image data, and the potential risk of illegal access and data theft is difficult to detect, this paper proposes an image encryption-compression ...
Qi Liang, Jia Duan, XinJie Hu, Wenxin Yu
doaj   +1 more source

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach   +23 more
wiley   +1 more source

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