Results 61 to 70 of about 4,090 (214)

Promising Research and Development Results in the Field of Image and Speech Signal Processing

open access: yesДоклады Белорусского государственного университета информатики и радиоэлектроники
An analysis of the prospects for the development of technologies for processing images and speech signals is presented. The main results in these areas obtained in recent years in the relevant scientific schools of Belarusian State University of ...
D. S. Likhachov   +4 more
doaj   +1 more source

TOUCHING GRAIN KERNELS SEPARATION BY GAP-FILLING

open access: yesImage Analysis and Stereology, 2011
Separation of touching grain kernels is a recurring problem in image analysis. Morphological methods to separatemerged objects in binary images are generally based on the watershed transformapplied to the inverse of the distance function.
Matthieu Faessel, Francis Courtois
doaj   +1 more source

Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce   +72 more
wiley   +1 more source

Color feature extraction of HER2 Score 2+ overexpression on breast cancer using Image Processing

open access: yesMATEC Web of Conferences, 2018
One of the major challenges in the development of early diagnosis to assess HER2 status is recognized in the form of Gold Standard. The accuracy, validity and refraction of the Gold Standard HER2 methods are widely used in laboratory (Perez, et al., 2014)
Muhimmah Izzati   +2 more
doaj   +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

MAGNET: Medial Axis Guided Network Extraction Tool

open access: yesInterPore Journal
Pore network models are useful for studying transport in porous materials in a computationally efficient way. Extraction of networks from volumetric images has evolved over the years, starting with medial axis-based approaches to more recent watershed ...
Michael McKague   +3 more
doaj   +1 more source

Longitudinal Assessment of Biomarkers in ALS: Discriminative Biomarkers for Disease Progression and Survival

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To assess the association and discriminative performance of serum biomarkers with clinical disease progression and survival in patients with amyotrophic lateral sclerosis (ALS). Methods This retrospective study, conducted at Houston Methodist Hospital, Houston, TX, used longitudinal serum samples collected between January 2018 and ...
David R. Beers   +7 more
wiley   +1 more source

Botanical tree reconstruction from a single image via 3D GAN-based skeletonization

open access: yesVirtual Reality & Intelligent Hardware
Background: 3D botanical tree reconstruction from a single image plays a vital role in the field of computer graphics. However, accurately capturing the intricate branching patterns and detailed morphologies of trees remains a challenge. Methods: In this
Chi Weng, MA   +3 more
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

Plasma EV Proteomics Identifies ECM Remodeling and Inflammatory Proteins LUM and C7 as Candidate Biomarkers in FSHD

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral muscular dystrophy (FSHD) is one of the most debilitating and common muscular dystrophies. Despite its severity, no approved therapy exists for FSHD patients. However, several therapeutic candidates are currently under development, and some have recently entered clinical trials, marking the need for reliable ...
Mustafa Bilal Bayazit   +11 more
wiley   +1 more source

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