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Articles

Since the Syn-One Test only needs a small punch skin biopsy that can be collected in an office setting, the clinical utility can be enhanced to offer more geographically convenient access for patients earlier in the disease.

Syn-One Test Displays Significant Clinical Utility for the Diagnosis of Synucleinopathies

Videos

A duo of experts discussed the importance of addressing barriers such as provider comfort, access to genetic counselors, and insurance coverage to reduce diagnostic latency and standardize genetic testing for epilepsy. [WATCH TIME: 5 minutes]

Improving Access and Reducing Latency in Genetic Testing for Epilepsy: Julie Ziobro, MD, PhD; John Schreiber, MD

Test your neurology knowledge with NeurologyLive®'s weekly quiz series, featuring questions on a variety of clinical and historical neurology topics. This week's topic is on CGRP medications to treat migraine.

NeurologyLive® Brain Games: December 22, 2024

The investigational therapy was safe, well-tolerated, and showed promising improvements in cognitive measures among patients with dementia with Lewy bodies.

CT1812 Meets Primary End Point in Phase 2 SHIMMER Study for Dementia with Lewy Bodies

Assistant professor of pediatrics at the University of Michigan.

Assistant professor of neurosurgery and neuroscience at Mayo Clinic Arizona

The assistant professor of neurosurgery and neuroscience at Mayo Clinic Arizona discussed an ongoing early-stage study assessing the therapeutic potential of NRTX-1001 nerve cell therapy in drug-resistant unilateral mesial temporal lobe epilepsy. [WATCH TIME: 5 minutes]

Studying Nerve Cell Therapy NRTX-1001 to Treat Mesial Temporal Lobe Epilepsy: Jonathan Parker, MD, PhD

, has been with the team since September 2022. Follow her on Twitter 

The program assembles a collaborative team of in-house and external experts in research, clinical care, and regulatory affairs to navigate gene therapy programs through the drug development process.

FDA Grants MDA Kickstart Program Rare Pediatric Disease Designation and Orphan Drug Designation in Congenital Myasthenic Syndrome

IJMSC Insights offers a closer look at the latest research and the people behind it from the community of the International Journal of Multiple Sclerosis Care (IJMSC) and the Consortium of Multiple Sclerosis Centers (CMSC).

IJMSC Insights: Blanca De Dios Perez on Employment and Multiple Sclerosis

NeurologyLive is your direct connection to the latest neurology news and interviews with expert neurologists in multimedia formats.

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Video Series

 Peer Exchange video series features panels of expert physicians engaging in in-depth discussions about practice-changing treatments, challenges in care, and the future paradigm of management for neurologic diseases.

Peer Exchange

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Understanding Hereditary ATTR (hATTR) Amyloidosis and the Recent Advances in Management

Defining hATTR Amyloidosis

Recognizing and Identifying hATTR Amyloidosis

Diagnosing hATTR Amyloidosis: Family History

Uncommon Presentations of hATTR Amyloidosis

Diagnostic Tests to Confirm hATTR Amyloidosis

Tissue Biopsies to Confirm hATTR Amyloidosis

Diagnosing hATTR Amyloidosis With Cardiomyopathy

Additional Testing for the Diagnosis of hATTR Amyloidosis

Genetic Testing in hATTR Amyloidosis

Gastrointestinal Manifestations in hATTR Amyloidosis

Treating hATTR Amyloidosis: Historical Overview

TTR Gene Silencing Drugs in hATTR Amyloidosis: Trial Data

Future Role of Transplantation in hATTR Amyloidosis

Treating hATTR Amyloidosis: Unmet Needs

Future Implications for Treating hATTR Amyloidosis

Diagnosing and Managing hATTR Amyloidosis: Unmet Needs