Match tier
Listed
Presence
Current · Arkansas
Last published
2022
Sources
OpenAlex · ORCID
Refreshed
2026-08-06
R
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Richard E Frye's research has focused on complex heterozygous polymerase gamma mutations and their relation to cerebral folate deficiency in a child with refractory partial status epilepticus. This work, published in 2022, involved a pediatric case study investigating the genetic underpinnings of a severe neurological condition. Frye collaborates with Raghu Ramakrishnaiah at the University of Arkansas for Medical Sciences, with one shared publication. Frye's scholarly output includes one publication, and he is noted as recently active in research.
Metrics
- Publications: 1
Selected Publications
-
Complex Heterozygous Polymerase Gamma Mutation and Cerebral Folate Deficiency in a Child with Refractory Partial Status (2022)
Collaboration Network
Top Collaborators
Debopam Samanta
University of Arkansas for Medical Sciences
1 shared publication
In database
- Complex Heterozygous Polymerase Gamma Mutation and Cerebral Folate Deficiency in a Child with Refractory Partial Status
Raghu Ramakrishnaiah
University of Arkansas for Medical Sciences
1 shared publication
In database
- Complex Heterozygous Polymerase Gamma Mutation and Cerebral Folate Deficiency in a Child with Refractory Partial Status
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