Maya Mattar

MD/Rheumatology Section chief

University Hospitals Cleveland Medical Center

United States

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About

Dr. Maya Mattar is the Section Chief of Rheumatology at the Louis Stokes Cleveland VA Medical Center in the United States. Her research focuses on autoimmune rheumatic diseases, with recent publications addressing topics such as the safety of accelerated infusion protocols for Rituximab and the impact of vitamin D levels on mortality in rheumatoid arthritis patients. Additionally, she has explored the immune responses to COVID-19 vaccination in patients with rheumatoid arthritis and the potential adverse events associated with these vaccines.

Articles (9)

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2024

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2024

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2024

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2023

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2023

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2023

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2022

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2022

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2022

Collaborators (1)

Shahdi Malakooti

Case Western Reserve University

UNITED STATES

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Maya Mattar

Research Interests

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Articles (9)

Anti-PL-12 anti-synthetase syndrome manifesting with multiple digital ischemia: Case report & review of the literature.

Implementation of an Accelerated Infusion Protocol (90-Minute Infusion) of Rituximab and Its Safety in Patients With Autoimmune Rheumatic Diseases at a Tertiary Veterans Affairs Center.

Higher Vitamin D Levels before Methotrexate Therapy Initiation Are Associated with Lower Subsequent Mortality in Patients with Rheumatoid Arthritis.

Rheumatoid arthritis and older age are associated with lower humoral and cellular immune response to primary series COVID-19 mRNA vaccine.

COVID-19 vaccination experience in patients with rheumatoid arthritis treated at a single VA medical center.

Financial Incentives Are Associated with Lower Likelihood of COVID-19 Vaccination in Northeast Ohio.

Red Cell Distribution Width and Absolute Lymphocyte Count Associate With Biomarkers of Inflammation and Subsequent Mortality in Rheumatoid Arthritis.

A Case Series on the COVID-19 Vaccines and Possible Immune-Related Adverse Events: A New Challenge for the Rheumatologists.

Transient elastography score is elevated during rheumatoid factor-positive chronic hepatitis C virus infection and rheumatoid factor decline is highly variable over the course of direct-acting antiviral therapy.

Collaborators (1)

Shahdi Malakooti

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