Alice F. Ford

Neurology

3400 Civic Center Boulevard
South Pavilion, 2nd Floor
Philadelphia, PA 19104

Last Updated: 09/26/2026

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Found 9 publications

Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy.

Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy.

Journal: Cell reports

Published: February 20, 2025

Implementation of a specialized neuroprognostication consultation program and associated provider attitudes: A survey-based study.

Implementation of a specialized neuroprognostication consultation program and associated provider attitudes: A survey-based study.

Journal: Resuscitation plus

Published: February 08, 2025

Vessel wall imaging in the diagnosis of antiphospholipid syndrome presenting as Moyamoya syndrome-A case report.

Vessel wall imaging in the diagnosis of antiphospholipid syndrome presenting as Moyamoya syndrome-A case report.

Journal: The neuroradiology journal

Published: April 15, 2024

Reliability of Past Medical History in a Single Hospital Participating in Get With The Guidelines-Stroke Registry.

Reliability of Past Medical History in a Single Hospital Participating in Get With The Guidelines-Stroke Registry.

Journal: Journal of the American Heart Association

Published: June 22, 2022

Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy.

Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy.

Journal: Cell reports

Published: August 04, 2021

Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy.

Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy.

Journal: Nature communications

Published: April 28, 2021

Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation.

Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation.

Journal: JCI insight

Published: February 04, 2021

Fleeting Amyloid-like Forms of Rim4 Ensure Meiotic Fidelity.

Fleeting Amyloid-like Forms of Rim4 Ensure Meiotic Fidelity.

Journal: Cell

Published: October 10, 2015

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS.

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS.

Journal: Nature

Published: January 05, 2012

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Last Updated: 09/26/2026