Jimmy Holder, Kaifang Pang, Michel Weiwer, Kihoon Han, Wei Wang, Theresa Estiphan et al. Dysfunction of D2 dopamine receptor expressing neurons underlies manic-like behaviors in mice modeling SHANK3 duplication disorder, 12 July 2021, PREPRINT (Version 1) available at Research Square [https://doi.org/10.21203/rs.3.rs-646721/v1]
Estiphan T, Joshi C. (2022). Epilepsy with Myoclonic-Atonic Seizures (Doose Syndrome). Child Neurology Foundation. [Online]. Available at: [https://www.childneurologyfoundation.org/disorder/epilepsy-with-myoclonic-atonic-seizures- doose-syndrome/]
Estiphan T, Sturza J, Shellhaas R, Carlson M. (2022). A novel clinical risk scoring system for neurodevelopmental outcomes among survivors of neonatal hypoxic-ischemic encephalopathy (HIE). Poster presented at: Neuroscience Day, University of Michigan; Ann Arbor, MI. Pub Status: Accepted.
Carrasco M, Estiphan T, McNamara N. (2021). Paroxysmal Disorders In Infancy and Seizure Likelihood. Poster presented at: Neuroscience Day, University of Michigan; Ann Arbor, MI and at AES. Pub Status: Draft.
Charuta Joshi, Michael Ciliberto, Theresa Estiphan, Nancy McNamara, Scott Demarest, Eric Kossoff, Elaine Wirrell, Katherine Nickels. EMAS Through the Lens of PERC: What Works. [abstract submitted to AES, published Nov 22, 2021].
Malik S, Dang L, Fedak E, Patel N, Estiphan T, Garton H, Leber S, Altshuler D. (2019). EEG findings resemble seizures in slit-ventricle syndrome. Presented at: Neuroscience Day, University of Michigan; Ann Arbor, MI.
Estiphan TA, Gropman A, Chiaramello A. (2018). Use of butyrates to promote nuclear and mitochondrial metabolic reprogramming by boosting mitochondrial biogenesis in fibroblasts from patients with mitochondrial disease. Poster presented at: Research and Education Week, Children’s National; Washington, DC.
Estiphan TA, Wehbeh A, Rida K, El-Rifai O, Majarian T, Usta J, Barada K. (2014). Phenotype- Genotype correlation in Wilson’s disease in a huge Lebanese family: Hepatic presentation of patients who are compound heterozygous for P767Pfs/A1003T mutations. Poster presented at: Research Day, Lebanese Medical Students' International Committee (LeMSIC) in collaboration with Alpha Omega Alpha; Beirut, Lebanon.
