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TESS Research Foundation

Alternate name: TESS Research Foundation for Slc13a5 Epilepsy
ROR: 02z5vhz28
OpenAlex ID: I4405271751
Epilepsy and EEG Phenotype of SLC13A5 Citrate Transporter Disorder
2020 · Qian-Zhou Yang, Emily M. Spelbrink, et al. · Child Neurology Open · 38
SLC13A5 Deficiency Disorder: From Genetics to Gene Therapy
2022 · Kimberly Goodspeed, Judy S. Liu, et al. · Genes · 20
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Growth and Overall Health of Patients with SLC13A5 Citrate Transporter Disorder
2021 · Tanya L. Brown, Kimberly L. Nye, et al. · Metabolites · 20
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Characterizing a rare neurogenetic disease, SLC13A5 citrate transporter disorder, utilizing clinical data in a cloud-based medical record collection system
2023 · Emily M. Spelbrink, Tanya L. Brown, et al. · Frontiers in Genetics · 17
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The growing research toolbox for SLC13A5 citrate transporter disorder: a rare disease with animal models, cell lines, an ongoing Natural History Study and an engaged patient advocacy organization
2024 · Tanya L. Brown, Matthew N. Bainbridge, et al. · Therapeutic Advances in Rare Disease · 6
American Epilepsy Society Clinical Practice Guideline: Infantile Epilepsy
2026 · Daniel Freedman, Ifeoluwa Babatunde, et al. · Epiliepsy currents/Epilepsy currents · 5
Developmental phenotype and quality of life in SLC13A5 citrate transporter disorder
2024 · Can Ozlu, Raegan M. Adams, et al. · Developmental Medicine & Child Neurology · 3
Sleep Abnormalities in SLC13A5 Citrate Transporter Disorder
2024 · Raegan M. Adams, Can Ozlu, et al. · Genes · 2
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SLC13A5 citrate transporter disorder epilepsy phenotype
2025 · Can Ozlu, Emily M. Spelbrink, et al. · Epilepsy Research · 1
Works count: 9
Citation count: 199
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