Mark Fitzgerald

Assistant Professor of Clinical Neurology

United States

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Mark Fitzgerald is an Assistant Professor of Clinical Neurology at The Children's Hospital of Philadelphia Division of Neurology. His research focuses on neonatal neurology, particularly in the areas of epilepsy, neurodevelopmental disorders, and the implications of genetic factors. Recent articles include studies on SCN8A-related epilepsy and predictive models for neonatal seizures.

Articles (12)

Year:

2025

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2025

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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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2023

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2021

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2021

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2021

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2021

Collaborators (9)

Aster Harder

Leiden University Medical Center

NETHERLANDS

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Anna Jansen

University of Antwerp

BELGIUM

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Stéphanie Baulac

Sorbonne Université

FRANCE

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Christina Engel Høi-Hansen

Professor

University of Copenhagen

DENMARK

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Sudha Kessler

Associate Professor

University of Pennsylvania

UNITED STATES

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william james

Professor Emeritus

University of Pennsylvania

UNITED STATES

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Sherry Ershadi

Boston University

UNITED STATES

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Joris Vriens

PI/ professor

KU Leuven

BELGIUM

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Guido Rubboli

Københavns Universitet

DENMARK

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Mark Fitzgerald

Research Interests

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About

Articles (12)

Mosaic Ring 20 Syndrome

Development of a model to predict electroencephalographic seizures in neonates with hypoxic ischemic encephalopathy treated with therapeutic hypothermia

Global modified Delphi consensus on diagnosis, phenotypes, and treatment of SCN8A‐related epilepsy and/or neurodevelopmental disorders

Global modified‐Delphi consensus on comorbidities and prognosis of SCN8A‐related epilepsy and/or neurodevelopmental disorders

A quality improvement initiative to improve folic acid supplementation counseling for adolescent females with epilepsy.

Leveraging electronic medical record-embedded standardised electroencephalogram reporting to develop neonatal seizure prediction models: a retrospective cohort study.

Gain-of-function variants in the ion channel gene <i>TRPM3</i> underlie a spectrum of neurodevelopmental disorders.

Neonatal Hypertonia and Progressive Respiratory Failure due to Novel Heterozygous Mutation in ATAD1.

Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications

Periodic and rhythmic patterns in critically ill children: Incidence, interrater agreement, and seizures.

KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum

Expanding Access to Continuous EEG Monitoring in Neonatal Intensive Care Units.

Collaborators (9)

Aster Harder

Anna Jansen

Stéphanie Baulac

Christina Engel Høi-Hansen

Sudha Kessler

william james

Sherry Ershadi

Joris Vriens

Guido Rubboli

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