Related Experiment Video

Updated: Aug 27, 2025

Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model
05:12

Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model

Published on: September 4, 2017

11.0K

Cervical myelopathy revealing familial KRIT-1-mutated cerebrospinal cavernous malformations

B Guyot1, A Faivre1, A Sellier1

  • 1Department of neurosurgery, Sainte-Anne Military Hospital, Toulon, France.

Revue Neurologique
|September 24, 2022
PubMed
Abstract

No abstract available in PubMed .

More Related Videos

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on: August 8, 2022

3.4K
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

8.7K

Related Experiment Videos

Last Updated: Aug 27, 2025

Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model
05:12

Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model

Published on: September 4, 2017

11.0K
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on: August 8, 2022

3.4K
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

8.7K

Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

37
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
37

Articles linked to this work by shared authors, journal, and citation graph.

Return to duty after non-surgical treatment of a non-neurological thoracic or lumbar spine fracture in French military patients: a retrospective analysis of 54 patients.

BMJ military health·2025

French mobile neurosurgical unit: a retrospective analysis of 22 years of mission.

BMJ military health·2024

Nocardia farcinica cerebral abscess: A systematic review of treatment strategies.

Neuro-Chirurgie·2021

Evaluation of neurosurgical training of French military surgeons prior to their deployment.

Neuro-Chirurgie·2021

A choroid plexus metastasis of a prostatic adenocarcinoma mimicking a choroid plexus carcinoma: A case report.

Neuro-Chirurgie·2021

A new agarose-based microsystem to investigate cell response to prolonged confinement.

Lab on a chip·2020

Effect of levodopa-carbidopa intestinal gel infusion on objective measures of daytime sleepiness and nocturnal sleep in Parkinson's disease.

Revue neurologique·2026

Passive digital monitoring via mobile apps and wearables in multiple sclerosis: A systematic review.

Revue neurologique·2026

The Kernohan-Woltman notch phenomenon model of brainstem injury: Etiopathogenic classification and clinical outcome.

Revue neurologique·2026

Cardiovascular autonomic dysfunction in Morvan syndrome: A comparative study of heart rate variability and cardiovascular autonomic reflex tests.

Revue neurologique·2026

Prognostic value of stroke etiology following bridging therapy with tenecteplase: A TETRIS analysis.

Revue neurologique·2026

Starting from the syndrome: A comprehensive review on mononeuropathy multiplex.

Revue neurologique·2026

An intractable case of primary intra-axial central nervous system Rosai-Dorfman disease.

Surgical neurology international·2026

Urinary dysfunction following single-level lumbar fusion in men: A propensity-matched analysis of surgical approach.

Surgical neurology international·2026

Associations Between Renal Function, Uremic Toxins, and Cognitive Performance in Patients with Chronic Kidney Disease: A Pilot Study.

International journal of medical sciences·2026

Atlantoaxial dislocation in a patient with Neurofibromatosis type 1: Case report and review.

Surgical neurology international·2026

Glomus tumor of the thigh mimicking nerve sheath tumor: A report of two cases and review of literature.

Surgical neurology international·2026

Rapid Eye Movement Sleep-Related Indicators with Promising Performance in Diagnosing Narcolepsy.

Nature and science of sleep·2026
See all related articles
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies
Jove
Visualize
Contact Us