Dr. Avula is on Doximity
As a Doximity member you'll join over two million verified healthcare professionals in a private, secure network.
- Gain access to free telehealth tools, such as our “call shielding” and one-way patient texting.
- Connect with colleagues in the same hospital or clinic.
- Read the latest clinical news, personalized to your specialty.
Office
330 N saba street
San Antonio, TX 78207
Summary
- Dr. Sreenivas Kumar Avula is a Pediatrician based in San Antonio Texas specializing in Child Neurology. He completed his Pediatric Residency and Child Neurology Fellowship at the Cleveland Clinic Foundation between 2010 and 2015, after graduating from Kakatiya Medical College NTR in 2004. Dr. Avula has contributed to various publications. Notably, he published a case study on epilepsy in Child Neurology Open in 2022, research on a mutation in the FBXL4 gene in the Journal of the Neurological Sciences in 2020, and a study on mitochondrial disorder treatments in Current Treatment Options in Neurology in 2014. His publications have been cited by other works numerous times.
Education & Training
Cleveland Clinic FoundationFellowship, Child Neurology, 2012 - 2015- Cleveland Clinic FoundationResidency, Pediatrics, 2010 - 2012
Kakatiya Medical College NTRClass of 2004
Certifications & Licensure
TX State Medical License 2021 - 2026
IL State Medical License 2015 - 2023
OH State Medical License 2010 - 2016- American Board of Psychiatry and Neurology Neurology with Special Qualification in Child Neurology
- American Board of Psychiatry and Neurology Epilepsy
Publications & Presentations
PubMed
- 57 citationsTreatment of mitochondrial disorders.Sreenivas Avula, Sumit Parikh, Scott Demarest, Jonathan E. Kurz, Andrea L. Gropman
Current Treatment Options in Neurology. 2014-04-04 - 12 citationsCharacterization of Co-Formulated High-Concentration Broadly Neutralizing Anti-HIV-1 Monoclonal Antibodies for Subcutaneous Administration.Vaneet K. Sharma, Bijay Misra, Kevin T McManus, Sreenivas Avula, Kaliappanadar Nellaiappan
Antibodies. 2020-07-29 - 9 citationsNovel homozygous mutation in the FBXL4 gene is associated with mitochondria DNA depletion syndrome-13.Simei Wang, Longlong Lin, Yilin Wang, Anqi Wang, Zhao Liu
Journal of the Neurological Sciences. 2020-09-15
Viewing the full profile is available to verified healthcare professionals only.
Find your profile and take control of your online presence:
