Luke F. O'donnell - Publications

Evaluating Hospital Course Summarization by an Electronic Health Record-Based Large Language Model.

Journal: JAMA network open

Published: August 13, 2025

Peripheral Neuropathy in p.Val142Ile (Val122Ile) Variant Hereditary Transthyretin-Mediated Amyloidosis: United Kingdom Experience.

Journal: Neurology. Genetics

Published: April 16, 2025

Skin Biopsy as a Diagnostic Tool for ATTRv Amyloid Neuropathy in the UK.

Journal: Journal of the peripheral nervous system : JPNS

Published: January 25, 2025

Reference Ranges for All: Implementing Reference Ranges for Transgender and Nonbinary Patients.

Journal: Applied clinical informatics

Published: December 18, 2024

A complex and severe encephalitis associated with four co-existing neuronal cell-surface autoantibodies.

Journal: Journal of neuroimmunology

Published: September 21, 2024

Serum neurofilament light chain in hereditary transthyretin amyloidosis: validation in real-life practice.

Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis

Published: February 13, 2024

Quantitative Foot Muscle Magnetic Resonance Imaging Reliably Measures Disease Progression in Children and Adolescents with Charcot-Marie-Tooth Disease Type 1A.

Journal: Annals of neurology

Published: January 25, 2024

Digenic FLNA and UCHL1 variants resulting in a complex phenotype.

Journal: Journal of the peripheral nervous system : JPNS

Published: October 31, 2023

Quantitative MRI outcome measures in CMT1A using automated lower limb muscle segmentation.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: August 18, 2023

Exploratory analysis of lower limb muscle MRI in a case series of patients with SORD neuropathy.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: April 14, 2022

Factors associated with hospital admission and critical illness among 5279 people with coronavirus disease 2019 in New York City: prospective cohort study.

Journal: BMJ (Clinical research ed.)

Published: May 24, 2020

Chronic Progressive External Ophthalmoplegia due to a Rare de novo m.12334G>A MT-TL2 Mitochondrial DNA Variant1.

Journal: Journal of neuromuscular diseases

Published: April 21, 2020