StuartMFraserMD
Child Neurology • Houston, TXPediatric Vascular Neurology
Assistant Professor of Pediatric Neurology
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Office
6431 Fannin St
# Msb
Houston, TX 77030Phone+1 713-500-5800Fax+1 713-500-5805
Summary
- I am a pediatric vascular neurologist and director of the pediatric stroke program at University of Texas McGovern Medical School Department of Pediatrics, Division of Child Neurology
Education & Training
University of Texas Health Science Center at HoustonFellowship, Vascular Neurology, 2021 - 2022- University of Texas Health Science Center at HoustonResidency, Child Neurology, 2018 - 2021
- University of Texas Health Science Center at HoustonResidency, Pediatrics, 2017 - 2020
McGovern Medical School at UTHealthClass of 2016
Certifications & Licensure
TX State Medical License 2018 - 2025- American Board of Psychiatry and Neurology Neurology with Special Qualification in Child Neurology
- American Board of Psychiatry and Neurology Vascular Neurology
Awards, Honors, & Recognition
- Alpha Omega Alpha Medical Honor Society Member Alpha Omega Alpha Medical Honor Society, 2020
- William E. Pasteur Memorial Scholarship University of Texas McGovern Medical School, 2015
- Margarett Root Brown Scholarship The Brown Foundation, 2012
Clinical Trials
- Perinatal Arterial Stroke: A Multi-site RCT of Intensive Infant Rehabilitation (I-ACQUIRE) Start of enrollment: 2019 Oct 10
Roles: Contact, Principal Investigator
- TOlerability of Transcranial Direct Current Stimulation in Pediatric Stroke Survivors Start of enrollment: 2023 Jun 30
Roles: Principal Investigator, Contact
Publications & Presentations
PubMed
- 2 citationsEstablishing a pediatric acute stroke protocol: experience of a new pediatric stroke program and predictors of acute stroke.Kamal Phelps, Christin Silos, Susan De La Torre, Amee Moreno, Robert Lapus
Frontiers in Neurology. 2023-01-01 - 11 citationsRare variants in ANO1, encoding a calcium-activated chloride channel, predispose to moyamoya disease.Amélie Pinard, Wenlei Ye, Stuart M Fraser, Jill A Rosenfeld, Pavel Pichurin
Brain. 2023-09-01 - 1 citationsSAMHD1 compound heterozygous rare variants associated with moyamoya and mitral valve disease in the absence of other features of Aicardi-Goutières syndrome.Aamuktha R Karla, Amélie Pinard, Maura L Boerio, Dimitri Hemelsoet, Simon J Tavernier
American Journal of Medical Genetics. Part A. 2024-04-01
Press Mentions
I-ACQUIRE in UT InstagramSeptember 22nd, 2021
Grant Support
- T32 Training GrantNIH2022–2024
- T32 Training GrantNIH2021–2022
Professional Memberships
- Member
- Member
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