Hannah Barkley
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Researcher
Graduate Student Researcher
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Hannah Barkley's research has focused on medical case studies and health sciences education. She has co-authored publications addressing profound hypotonia in infants with δ-aminolevulinic acid dehydratase deficient porphyria. Barkley has also contributed to research on quality improvement training within pediatric residency programs and the implementation of evaluation systems in a single institution.
Her scholarly work includes two publications, with her most recent appearing in 2025. Barkley collaborates with researchers at the University of Arkansas for Medical Sciences, including Carissa Rodriquez, Abhay A. Shukla, T. Burrow, and Alexis N. Roach, with whom she shares three co-authored publications.
Metrics
- Publications: 2
Selected Publications
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Creating a Roadmap for Longitudinal Quality Improvement Training in a Pediatric Residency Program (2025)
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Correction: Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria (2025)
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Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria (2024)
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04145 Profound hypotonia in a newborn with Biallelic δ-Aminolevulinic Acid Dehydratase (ALAD) mutations (2024)
Collaboration Network
Top Collaborators
- Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- 04145 Profound hypotonia in a newborn with Biallelic δ-Aminolevulinic Acid Dehydratase (ALAD) mutations
- Correction: Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- 04145 Profound hypotonia in a newborn with Biallelic δ-Aminolevulinic Acid Dehydratase (ALAD) mutations
- Correction: Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- 04145 Profound hypotonia in a newborn with Biallelic δ-Aminolevulinic Acid Dehydratase (ALAD) mutations
- Correction: Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- 04145 Profound hypotonia in a newborn with Biallelic δ-Aminolevulinic Acid Dehydratase (ALAD) mutations
- Correction: Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- Correction: Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- 04145 Profound hypotonia in a newborn with Biallelic δ-Aminolevulinic Acid Dehydratase (ALAD) mutations
- Creating a Roadmap for Longitudinal Quality Improvement Training in a Pediatric Residency Program
- Creating a Roadmap for Longitudinal Quality Improvement Training in a Pediatric Residency Program
- Creating a Roadmap for Longitudinal Quality Improvement Training in a Pediatric Residency Program
- Creating a Roadmap for Longitudinal Quality Improvement Training in a Pediatric Residency Program
- Creating a Roadmap for Longitudinal Quality Improvement Training in a Pediatric Residency Program
- Creating a Roadmap for Longitudinal Quality Improvement Training in a Pediatric Residency Program
- Creating a Roadmap for Longitudinal Quality Improvement Training in a Pediatric Residency Program
- Creating a Roadmap for Longitudinal Quality Improvement Training in a Pediatric Residency Program
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