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Page 1
Developmental phenotype and quality of life in SLC13A5 citrate transporter disorder.
Ozlu C, Adams RM, Solidum RM, Cooper S, Best CR, Elacio J, Kavanaugh BC, Spelbrink EM, Brown TL, Nye K, Liu JS, Bailey RM, Goodspeed K, Porter BE. Ozlu C, et al. Among authors: solidum rm. Dev Med Child Neurol. 2025 Jul;67(7):930-940. doi: 10.1111/dmcn.16218. Epub 2024 Dec 22. Dev Med Child Neurol. 2025. PMID: 39710583
Drug-Resistant Epilepsy in Tuberous Sclerosis Complex Is Associated With TSC2 Genotype: More Findings From the Preventing Epilepsy Using Vigatrin (PREVeNT) Trial.
Farach LS, Richard MA, Wulsin AC, Bebin EM, Krueger DA, Sahin M, Porter BE, McPherson TO, Peters JM, O'Kelley S, Taub KS, Rajaraman R, Randle SC, McClintock WM, Koenig MK, Frost MD, Werner K, Nolan DA, Wong M, Cutter G, Northrup H, Au KS; PREVeNT Study Group. Farach LS, et al. Pediatr Neurol. 2024 Oct;159:62-71. doi: 10.1016/j.pediatrneurol.2024.06.012. Epub 2024 Jul 4. Pediatr Neurol. 2024. PMID: 39142021
Sleep Abnormalities in SLC13A5 Citrate Transporter Disorder.
Adams RM, Ozlu C, Bailey LE, Solidum RM, Cooper S, Best CR, Elacio J, Kavanaugh BC, Brown TL, Nye K, Liu J, Porter BE, Goodspeed K, Bailey RM. Adams RM, et al. Among authors: solidum rm. Genes (Basel). 2024 Oct 18;15(10):1338. doi: 10.3390/genes15101338. Genes (Basel). 2024. PMID: 39457462 Free PMC article.