Publications by authors named "Erika Finanger"

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Long-Term Evaluation of Givinostat in Duchenne Muscular Dystrophy, and Natural History Comparisons.
Craig M McDonald, Michela Guglieri, Dragana Vučinić, Gyula Acsadi, John F Brandsema, Erika L Finanger

Ann Clin Transl Neurol· November 2025

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New hope for older SMA patients with next-generation self-complementary AAV gene therapy.
Hiroyuki Nakai, Erika L Finanger, Richard Jude Samulski

Mol Ther· October 2025

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Characterization of severe COL6-related dystrophy due to the recurrent variant COL6A1 c.930+189C>T.
A Reghan Foley, Véronique Bolduc, Fady Guirguis, Sandra Donkervoort, Ying Hu, Erika Finanger

Brain· September 2025

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The recurrent deep intronic pseudoexon-inducing variant c.930+189C>T results in a consistently severe phenotype of COL6-related dystrophy: Towards clinical trial readiness for splice-modulating therapy.
A Reghan Foley, Véronique Bolduc, Fady Guirguis, Sandra Donkervoort, Ying Hu, Erika Finanger

medRxiv· March 2024

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Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Lauren Jeffries, Emily K Mis, Kirsty McWalter, Sandra Donkervoort, Nina N Brodsky, Erika Finanger

Genet Med· February 2024

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Clinical importance of changes in magnetic resonance biomarkers for Duchenne muscular dystrophy.
Rebecca J Willcocks, Alison M Barnard, Michael J Daniels, Sean C Forbes, William T Triplett, Erika L Finanger

Ann Clin Transl Neurol· January 2024

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Step Activity Monitoring in Boys with Duchenne Muscular Dystrophy and its Correlation with Magnetic Resonance Measures and Functional Performance.
Kavya S Nair, Donovan J Lott, Sean C Forbes, Alison M Barnard, Rebecca J Willcocks, Erika L Finanger

J Neuromuscul Dis· May 2022

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Development of Contractures in DMD in Relation to MRI-Determined Muscle Quality and Ambulatory Function.
Rebecca J Willcocks, Alison M Barnard, Ryan J Wortman, Claudia R Senesac, Donovan J Lott, Erika L Finanger

J Neuromuscul Dis· March 2022

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A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy: Results of the PolarisDMD Trial.
Richard S Finkel, Craig M McDonald, H Lee Sweeney, Erika Finanger, Erin Neil Knierbein

J Neuromuscul Dis· November 2021

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Disease-modifying effects of edasalonexent, an NF-κB inhibitor, in young boys with Duchenne muscular dystrophy: Results of the MoveDMD phase 2 and open label extension trial.
Richard S Finkel, Erika Finanger, Krista Vandenborne, H Lee Sweeney, Gihan Tennekoon

Neuromuscul Disord· May 2021

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Walking activity in a large cohort of boys with Duchenne muscular dystrophy.
Donovan J Lott, Tanja Taivassalo, Claudia R Senesac, Rebecca J Willcocks, Ann M Harrington, Erika L Finanger

Muscle Nerve· February 2021

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Upper and Lower Extremities in Duchenne Muscular Dystrophy Evaluated with Quantitative MRI and Proton MR Spectroscopy in a Multicenter Cohort.
Sean C Forbes, Harneet Arora, Rebecca J Willcocks, William T Triplett, William D Rooney, Erika L Finanger

Radiology· June 2020

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Modeling disease trajectory in Duchenne muscular dystrophy.
William D Rooney, Yosef A Berlow, William T Triplett, Sean C Forbes, Rebecca J Willcocks, Erika L Finanger

Neurology· April 2020

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MR biomarkers predict clinical function in Duchenne muscular dystrophy.
Alison M Barnard, Rebecca J Willcocks, William T Triplett, Sean C Forbes, Michael J Daniels, Erika L Finanger

Neurology· March 2020

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Phase 1 Study of Edasalonexent (CAT-1004), an Oral NF-κB Inhibitor, in Pediatric Patients with Duchenne Muscular Dystrophy.
Erika Finanger, Krista Vandenborne, Richard S Finkel, H Lee Sweeney, Gihan Tennekoon

J Neuromuscul Dis· January 2020

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Longitudinal timed function tests in Duchenne muscular dystrophy: ImagingDMD cohort natural history.
Harneet Arora, Rebecca J Willcocks, Donovan J Lott, Ann T Harrington, Claudia R Senesac, Erika L Finanger

Muscle Nerve· November 2018

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Two-Year Longitudinal Changes in Lower Limb Strength and Its Relation to Loss in Function in a Large Cohort of Patients With Duchenne Muscular Dystrophy.
Abhinandan Batra, Ann Harrington, Donovan J Lott, Rebecca Willcocks, Claudia R Senesac, Erika Finanger

Am J Phys Med Rehabil· October 2018

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Recruitment & retention program for the NeuroNEXT SMA Biomarker Study: Super Babies for SMA!
Amy Bartlett, Stephen J Kolb, Allison Kingsley, Kathryn J Swoboda, Sandra P Reyna, Erika Finanger

Contemp Clin Trials Commun· September 2018

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Skeletal muscle magnetic resonance biomarkers correlate with function and sentinel events in Duchenne muscular dystrophy.
Alison M Barnard, Rebecca J Willcocks, Erika L Finanger, Michael J Daniels, William T Triplett

PLoS One· July 2018

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Longitudinal ophthalmic findings in a child with Helsmoortel-Van der Aa Syndrome.
Michael J Gale, Hope E Titus, Gareth A Harman, Talal Alabduljalil, Anna Dennis, Erika Finanger

Am J Ophthalmol Case Rep· June 2018

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Natural history of infantile-onset spinal muscular atrophy.
Stephen J Kolb, Christopher S Coffey, Jon W Yankey, Kristin Krosschell, W David Arnold, Erika Finanger

Ann Neurol· December 2017

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Duvoglustat HCl Increases Systemic and Tissue Exposure of Active Acid α-Glucosidase in Pompe Patients Co-administered with Alglucosidase α.
Priya Kishnani, Mark Tarnopolsky, Mark Roberts, Kumarswamy Sivakumar, Majed Dasouki, Erika Finanger

Mol Ther· May 2017

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Case 3: Episodic Weakness in an 18-month-old Girl.
Matthew Dietz, Michael Jones, Melissa Svoboda, Erika Finanger

Pediatr Rev· May 2016

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Baseline results of the NeuroNEXT spinal muscular atrophy infant biomarker study.
Stephen J Kolb, Christopher S Coffey, Jon W Yankey, Kristin Krosschell, W David Arnold, Erika Finanger

Ann Clin Transl Neurol· February 2016

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