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Carolyn Elizabeth Pizoli, MD, PhD

Assistant Professor of Pediatrics
Affiliate of the Center for Brain Imaging and Analysis

My current research is focused on understanding the development of neural networks after acquired brain injury.

Education and Training

  • Resident in Child Neurology, Neurology, St. Louis Children's Hospital, 2006 - 2008
  • Resident in Neurology, Neurology, Barnes-Jewish Hospital, 2005 - 2006
  • Pediatric Internship and Residency, Pediatrics, St. Louis Children's Hospital, 2003 - 2005
  • Ph.D., Pennsylvania State University, 2003
  • M.D., Pennsylvania State University, 2003

Publications

Mangalesh, Shwetha, Du Tran-Viet, Carolyn Pizoli, Vincent Tai, Mays Antoine El-Dairi, Xi Chen, Christian Viehland, et al. “Subclinical Retinal versus Brain Findings in Infants with Hypoxic Ischemic Encephalopathy.” Graefes Arch Clin Exp Ophthalmol, May 29, 2020. https://doi.org/10.1007/s00417-020-04738-0.

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Trau, Steven P., and Carolyn E. Pizoli. “PURA Syndrome and Myotonia.” Pediatr Neurol 104 (March 2020): 62–63. https://doi.org/10.1016/j.pediatrneurol.2019.09.008.

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Berube, Megan W., Monica E. Lemmon, Carolyn E. Pizoli, Margarita Bidegain, Veeral N. Tolia, C Michael Cotten, and Rachel G. Greenberg. “Opioid and benzodiazepine use during therapeutic hypothermia in encephalopathic neonates.” J Perinatol 40, no. 1 (January 2020): 79–88. https://doi.org/10.1038/s41372-019-0533-4.

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Hansen, Adam W., Mullai Murugan, He Li, Michael M. Khayat, Liwen Wang, Jill Rosenfeld, B Kim Andrews, et al. “A Genocentric Approach to Discovery of Mendelian Disorders.” Am J Hum Genet 105, no. 5 (November 7, 2019): 974–86. https://doi.org/10.1016/j.ajhg.2019.09.027.

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Helbig, Katherine L., Robert J. Lauerer, Jacqueline C. Bahr, Ivana A. Souza, Candace T. Myers, Betül Uysal, Niklas Schwarz, et al. “De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.” Am J Hum Genet 104, no. 3 (March 7, 2019): 562. https://doi.org/10.1016/j.ajhg.2019.02.015.

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Khan, Tahir N., Kamal Khan, Azita Sadeghpour, Hannah Reynolds, Yezmin Perilla, Marie T. McDonald, William B. Gallentine, et al. “Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies.” Am J Hum Genet 104, no. 1 (January 3, 2019): 94–111. https://doi.org/10.1016/j.ajhg.2018.11.017.

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Herrera, Tamara I., Laura Edwards, William F. Malcolm, P Brian Smith, Kimberley A. Fisher, Carolyn Pizoli, Kathryn E. Gustafson, et al. “Outcomes of preterm infants treated with hypothermia for hypoxic-ischemic encephalopathy.” Early Hum Dev 125 (October 2018): 1–7. https://doi.org/10.1016/j.earlhumdev.2018.08.003.

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Tan, Queenie K-G, Allyn McConkie-Rosell, Jane Juusola, Kathryn E. Gustafson, Carolyn E. Pizoli, Anne F. Buckley, and Yong-Hui Jiang. “The importance of managing the patient and not the gene: expanded phenotype of GLE1-associated arthrogryposis.” Cold Spring Harb Mol Case Stud 3, no. 6 (November 2017). https://doi.org/10.1101/mcs.a002063.

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Pecoraro, Anthony, Eric Arehart, William Gallentine, Rodney Radtke, Edward Smith, Carolyn Pizoli, Sujay Kansagra, Elie Abdelnour, Roger McLendon, and Mohamad A. Mikati. “Epilepsy in neurofibromatosis type 1.” Epilepsy Behav 73 (August 2017): 137–41. https://doi.org/10.1016/j.yebeh.2017.05.011.

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Edwards, Laura, Stephen DeMeo, Chi D. Hornik, C Michael Cotten, P Brian Smith, Carolyn Pizoli, Julie M. Hauer, and Margarita Bidegain. “Gabapentin Use in the Neonatal Intensive Care Unit.” J Pediatr 169 (February 2016): 310–12. https://doi.org/10.1016/j.jpeds.2015.10.013.

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