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Christopher Troedson

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Ebiomedicine|April 29, 2023

CSF neopterin, quinolinic acid and kynurenine/tryptophan ratio are biomarkers of active neuroinflammationJingya Yan, Kavitha Kothur, Shekeeb Mohammad, et al.

Journal of Clinical Immunology|August 28, 2024

Hereditary C1q Deficiency is Associated with Type 1 Interferon-Pathway Activation and a High Risk of Central Nervous System InflammationClément Triaille, Neha Mohan Rao, Gillian I Rice, et al.

Stroke|June 25, 2025

Thrombectomy Versus Medical Management for Pediatric Arterial Ischemic Stroke With Large Baseline InfarctKartik D Bhatia, Prakash Muthusami, Carmen Parra-Farinas, et al.

Human Genetics|October 15, 2021

TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathyMary C Whitman, Brenda J Barry, Caroline D Robson, et al.

Annals of Neurology|August 22, 2023

GABRA1-Related Disorders: From Genetic to Functional PathwaysElisa Musto, Vivian W Y Liao, Katrine M Johannesen, et al.

Annals of Neurology|July 1, 2025

The Spectrum of Neurologic Phenotypes Associated With NUS1 Pathogenic Variants: A Comprehensive Case SeriesSarah M Brooker, Maria Novelli, Robert Coukos, et al.

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Search research articles

Showing results (31-40 of 36) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 36 results.

Ebiomedicine|April 29, 2023

CSF neopterin, quinolinic acid and kynurenine/tryptophan ratio are biomarkers of active neuroinflammationJingya Yan, Kavitha Kothur, Shekeeb Mohammad, et al.

Journal of Clinical Immunology|August 28, 2024

Hereditary C1q Deficiency is Associated with Type 1 Interferon-Pathway Activation and a High Risk of Central Nervous System InflammationClément Triaille, Neha Mohan Rao, Gillian I Rice, et al.

Stroke|June 25, 2025

Thrombectomy Versus Medical Management for Pediatric Arterial Ischemic Stroke With Large Baseline InfarctKartik D Bhatia, Prakash Muthusami, Carmen Parra-Farinas, et al.

Human Genetics|October 15, 2021

TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathyMary C Whitman, Brenda J Barry, Caroline D Robson, et al.

Annals of Neurology|August 22, 2023

GABRA1-Related Disorders: From Genetic to Functional PathwaysElisa Musto, Vivian W Y Liao, Katrine M Johannesen, et al.

Annals of Neurology|July 1, 2025

The Spectrum of Neurologic Phenotypes Associated With NUS1 Pathogenic Variants: A Comprehensive Case SeriesSarah M Brooker, Maria Novelli, Robert Coukos, et al.

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