Congenital and Acquired Chiari Syndrome

RM Friedlander - New England Journal of Medicine, 2024 - Mass Medical Soc
Symptomatic Chiari Malformation Type 1 Symptomatic CM1, also called the Chiari
syndrome, is characterized mainly by headache but also by numbness or weakness in the …

Digenic Inheritance of PROC and SERPINC1 Mutations Contributes to Multiple Sites Venous Thrombosis

X Li, J Zhu, W Ma, W Zhou, W Zhang - Hämostaseologie, 2024 - thieme-connect.com
Venous thromboembolism (VTE) represents a worldwide health challenge, impacting
millions of people each year. The genesis of venous thrombosis is influenced in part by …

[PDF][PDF] Exploring pathogenesis, prevalence, and genetic associations in Chiari malformation type 1: a contemporary perspective

SNM Rosdi, S Omar, MM Ghazali… - … : Research, Reviews and …, 2024 - sciendo.com
Abstract Chiari malformation type 1 (CM 1) entails a structural defect in the cerebellum,
involving the herniation of cerebellar tonsils toward the foramen magnum. The symptomatic …

[HTML][HTML] Chiari I malformation

CA Lee - JOURNAL OF INSURANCE MEDICINE-NEW YORK …, 2006 - medlink.com
Chiari malformation describes a group of structural defects of the cerebellum characterized
by brain tissue protruding into the spinal canal. Chiari malformations are often associated …