Results 101 to 110 of about 389,048 (398)

VertXNet: An Ensemble Method for Vertebrae Segmentation and Identification of Spinal X-Ray [PDF]

open access: yesarXiv, 2023
Reliable vertebrae annotations are key to perform analysis of spinal X-ray images. However, obtaining annotation of vertebrae from those images is usually carried out manually due to its complexity (i.e. small structures with varying shape), making it a costly and tedious process.
arxiv  

Cervical, Thoracic, and Spinopelvic Compensation After Proximal Junctional Kyphosis (PJK): Does Location of PJK Matter? [PDF]

open access: yes, 2020
Study Design:Retrospective case series. Objective:Compensatory changes above a proximal junctional kyphosis (PJK) have not been defined. Understanding these mechanisms may help determine optimal level selection when performing revision for PJK.
Ames, Christopher P   +14 more
core  

A procedure for implanting a spinal chamber for longitudinal in vivo imaging of the mouse spinal cord. [PDF]

open access: yes, 2014
Studies in the mammalian neocortex have enabled unprecedented resolution of cortical structure, activity, and response to neurodegenerative insults by repeated, time-lapse in vivo imaging in live rodents.
Farrar, Matthew J, Schaffer, Chris B
core   +2 more sources

Tall Stature and Scoliosis Associated With a Novel Homozygous Loss‐of‐Function Missense Variant in NPR3

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT NPR3‐related tall stature is characterized by tall stature, elongated big toes, and additional epiphyses in hand and foot bones. The condition is caused by biallelic loss‐of‐function variants affecting natriuretic peptide receptor 3 (NPR3). Five individuals from four different families have been reported.
Pierre Moffatt   +4 more
wiley   +1 more source

Vertebral Synostosis and its Clinical Importance: A Study in Dried Vertebrae of Gujarat Population [PDF]

open access: yesInternational Journal of Anatomy Radiology and Surgery, 2019
Introduction: The vertebral column possess two basic functions: provide protection to spinal cord and support the trunk, transmit body weight to the lower extremities. Two or more vertebrae that are normally separate may be fused to each other.
Sanjay K Vikani, Mayankkumar D Javia
doaj   +1 more source

The cause of axial rotation of the scoliotic spine [PDF]

open access: yes, 1991
To explain the cause of axial rotation in a scoliotic vertebral column, the influence of the gravitation force on a spine with a C-scoliosis has been investigated by means of a mechanical model. In this model the gravitation force takes hold of the three-
Cool, J.C.   +3 more
core   +2 more sources

Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Gorlin‐Goltz Syndrome (GGS) is a rare autosomal dominant genetic disorder encompassing a diverse range of clinical manifestations, including congenital anomalies and predisposition to cancer. Pathogenic variants in PTCH1 and SUFU account for up to 79% and 6% of cases, respectively. Currently, an estimated 15%–27% of individuals with a clinical
V. Taliercio   +13 more
wiley   +1 more source

Prevalence of Osseous Pathology in the Articular Process Articulations in the Equine Cervical and Cranial Thoracic Vertebrae

open access: yes, 2014
Reasons for performing study Osteoarthritis (OA) of the articular processes (APs) is recognised as a clinical condition in the equine cervical spine, but there is little information on the prevalence and distribution of OA in the APs of the cervical ...
N. Rombach, N. Stubbs, H. Clayton
semanticscholar   +1 more source

Accuracy of transcranial magnetic stimulation and a Bayesian latent class model for diagnosis of spinal cord dysfunction in horses [PDF]

open access: yes, 2020
Background: Spinal cord dysfunction/compression and ataxia are common in horses. Presumptive diagnosis is most commonly based on neurological examination and cervical radiography, but the interest into the diagnostic value of transcranial magnetic ...
Buczinski, Sebastien   +7 more
core   +1 more source

Ocular Findings as the Most Striking Manifestation of a SMAD3 Variant

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Loeys‐Dietz syndrome (LDS) is a heritable connective tissue disorder with variable expressivity. It is a multisystemic condition mainly characterized by a propensity for arterial aneurysms and dissections, skeletal manifestations, hypertelorism, bifid uvula, craniosynostosis, and cutaneous features.
Noémie Villeneuve‐Cloutier   +7 more
wiley   +1 more source

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