Spinal Cord Injuries

Spinal cord injury is a serious type of trauma and can cause temporary or permanent damage, including loss of muscle function, sensation, or autonomic functions. Here is the latest research on spinal cord injuries.

January 22, 2021

Superiority of thoracolumbar injury classification and severity score (TLICS) over AOSpine thoracolumbar spine injury classification for the surgical management decision of traumatic spine injury in the pediatric population.

European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society
Corentin DauleacFederico Di Rocco
January 21, 2021
Open Access

Transplantation of Human Neural Precursor Cells Reverses Syrinx Growth in a Rat Model of Post-Traumatic Syringomyelia.

Neurotherapeutics : the Journal of the American Society for Experimental NeuroTherapeutics
Ning XuErik Sundström
January 23, 2021

Spinal Cord Gray and White Matter Damage in Different Hereditary Spastic Paraplegia Subtypes.

AJNR. American Journal of Neuroradiology
K R ServelhereM C França
January 21, 2021
Comment / Editorial
Open Access

Exercise for people with SCI: so important but difficult to achieve.

Spinal Cord
Sonja de Groot, Rachel E Cowan
January 22, 2021

A clinical study regarding the outcomes of symptomatic spinal epidural haematoma after adult spinal deformity surgery.

JPMA. the Journal of the Pakistan Medical Association
Shao Qiang LiuQiang Qi
January 24, 2021

Savings of loss-of-life expectancy and lifetime medical costs from prevention of spinal cord injuries: analysis of nationwide data followed for 17 years.

Injury Prevention : Journal of the International Society for Child and Adolescent Injury Prevention
Wei-Chih LienJung-Der Wang
January 22, 2021
Case Report

[A case of cervical spinal cord injury following thyroidectomy].

Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
B Li, L Z Feng
January 21, 2021

Is autonomic dysreflexia a cause of respiratory dysfunction after spinal cord injury?

Spinal Cord Series and Cases
Maria João AndradePatrícia Cruz
January 23, 2021
Open Access

Standardizing fatigue-resistance testing during electrical stimulation of paralysed human quadriceps muscles, a practical approach.

Journal of Neuroengineering and Rehabilitation
Martin SchmollChristine Azevedo Coste
January 24, 2021
Review

Immunomodulatory Biomaterials and Their Application in Therapies for Chronic Inflammation-Related Diseases.

Acta Biomaterialia
Jayachandra Reddy NakkalaChangyou Gao
January 23, 2021

TRPM3 channels play roles in heat hypersensitivity and spontaneous pain after nerve injury.

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
Songxue SuTibor Rohacs
January 21, 2021

An uncommon breast metastasis of mediastinal neuroblastoma within a child: A case report.

The Breast Journal
Jihene FekiAfef Khanfir
January 19, 2021

Multichannel Bioactive Silk Nanofiber Conduits Direct and Enhance Axonal Regeneration after Spinal Cord Injury

ACS Biomaterials Science & Engineering
Renchuan YouMingzhong Li

Sign up to follow this feed and discover related papers.

Related Feeds

3D Cellular Models of Brain and Neurodegeneration

Brain organoids are three-dimensional in vitro cellular models of the brain that can recapitulate many processes such as the neurodevelopment. In addition, these organoids can be combined with other cell types, such as neurons and astrocytes to study their interactions in assembloids. Disease processes can also be modeled by induced pluripotent stem cell-derived organoids and assembloids from patients with neurodegenerative disorders. Discover the latest research on the models here.

ALS & FTD: TDP-43

TAR DNA-binding protein 43 (TDP-43) is a pathological protein identified in sporadic Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD). Here are the latest discoveries pertaining to TDP-43 and these diseases.

ALS: Genetics

Amyotrophic Lateral Sclerosis (ALS) is a progressive neurodegenerative disorder characterized by muscle weakness. ALS is a genetically heterogeneous disorder with several causative genes. Here are the latest discoveries pertaining to the genetics of this disease.

ALS: Pathogenic Mechanisms

Amyotrophic Lateral Sclerosis is a progressive neurodegenerative disorder characterized by muscle weakness. Here is the latest research investigating pathogenic mechanisms that underlie this genetically heterogeneous disorder.

ALS: Phenotypes

Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disorder characterized phenotypically by progressive muscle weakness. Clinical phenotypes of ALS can be classified based on the pattern, level, and area of onset (e.g. bulbar, cervical, lumbar). Here is the latest research investigating phenotypes of ALS.

ALS: Prions

Prions are misfolded proteins which characterize several fatal neurodegenerative diseases. Prion-like mechanisms are associated with the pathogenesis of Amyotrophic Lateral Sclerosis (ALS). Here is the latest research on ALS and prions.

ALS: Stress Granules

Amyotrophic Lateral Sclerosis (ALS) is a neurodegenerative disease characterized by cytoplasmic protein aggregates within motor neurons. TDP-43 is an ALS-linked protein that is known to regulate splicing and storage of specific mRNAs into stress granules, which have been implicated in formation of ALS protein aggregates. Here is the latest research in this field.

ALS: Therapies

Amyotrophic Lateral Sclerosis (ALS) is associated with the death of neurons that control voluntary muscles. This feed followes the latest research into therapies for this progressive neurodegenerative disease.

Age-related Dementia

Dementias are a group of conditions, including Alzheimer's disease, vascular dementia, and frontotemporal dementia, characterized by deficiencies in cognitive abilities. Age-related dementia refers to dementias that occur in older individuals, usually 60+ years old, in contrast to early-onset dementia. Follow the latest research on age-related dementia here.

Alexander Disease

Alexander disease is a rare leukodystrophy caused by mutations in the astrocyte-specific intermediate filament protein glial fibrillary acidic protein (GFAP). Here is the latest research on this disease.

© 2021 Meta ULC. All rights reserved
/feed-previews/spinal-cord-injuries/b377ac90-79b6-4d26-8778-999c8ca36e1a