Scholars@Duke

• Background
• 

  Education, Training, & Certifications

  • Post-doctoral Research Associate, Medical Genetics/Pediatrics, Duke University School of Medicine 2017 - 2021
  • Resident-in -Training Clinical Cardiology, Asian Heart Institute (India) 2010 - 2012
  • M.B.B.S., Maharashtra University of Health Sciences, Nashik (India) 2010
• Expertise
• 

  Subject Headings

  • Glycogen Storage Disease Type II
  • Medical Writing
  • Natural history projects
  • Pediatric neurology--Research
• Research
• 

  Selected Grants

  • Understanding cognitive and neurological pathologies in infantile Pompe disease CNS awarded by Genzyme Corporation 2022 - 2024
  • Understanding cognitive and neurological pathologies in infantile Pompe disease CNS awarded by Genzyme Corporation 2019 - 2021
• Publications & Artistic Works
• 

  Selected Publications

  • Academic Articles

    • Crisp, Kelly D., Amy T. Neel, Sathya Amarasekara, Jill Marcus, Gretchen Nichting, Aditi Korlimarla, Priya S. Kishnani, and Harrison N. Jones. “Assessment of Dysphonia in Children with Pompe Disease Using Auditory-Perceptual and Acoustic/Physiologic Methods.” J Clin Med 10, no. 16 (August 16, 2021). https://doi.org/10.3390/jcm10163617.
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    • Korlimarla, Aditi, Jeong-A Lim, Paul McIntosh, Kanecia Zimmerman, Baodong D. Sun, and Priya S. Kishnani. “New Insights into Gastrointestinal Involvement in Late-Onset Pompe Disease: Lessons Learned from Bench and Bedside.” J Clin Med 10, no. 15 (July 30, 2021). https://doi.org/10.3390/jcm10153395.
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    • Korlimarla, Aditi, Jeong-A Lim, Paul McIntosh, Baodong Sun, and Priya S. Kishnani. “New insights into GI manifestations in late-onset Pompe disease: Lessons from the bench and bedside.” Molecular Genetics and Metabolism 132, no. 2 (February 2021): S58–59. https://doi.org/10.1016/j.ymgme.2020.12.130.
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    • Korlimarla, Aditi, Gail A. Spiridigliozzi, Mihaela Stefanescu, Stephanie L. Austin, and Priya S. Kishnani. “Behavioral, social and school functioning in children with Pompe disease.” Mol Genet Metab Rep 25 (December 2020): 100635. https://doi.org/10.1016/j.ymgmr.2020.100635.
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    • Korlimarla, Aditi, Gail A. Spiridigliozzi, Kelly Crisp, Mrudu Herbert, Steven Chen, Michael Malinzak, Mihaela Stefanescu, et al. “Novel approaches to quantify CNS involvement in children with Pompe disease.” Neurology 95, no. 6 (August 11, 2020): e718–32. https://doi.org/10.1212/WNL.0000000000009979.
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    • Korlimarla, Aditi, Jeong-A Lim, Priya S. Kishnani, and Baodong Sun. “An emerging phenotype of central nervous system involvement in Pompe disease: from bench to bedside and beyond.” Ann Transl Med 7, no. 13 (July 2019): 289. https://doi.org/10.21037/atm.2019.04.49.
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    • Korlimarla, A., S. Austin, B. Sun, and P. Kishnani. “Hepatic Manifestations in Glycogen Storage Disease Type III.” Current Pathobiology Reports 6, no. 4 (December 1, 2018): 233–40. https://doi.org/10.1007/s40139-018-0182-x.
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  • Book Sections

    • Korlimarla, Aditi, Priya Kishnani, and Rebecca Gibson. “Glycogen Storage Diseases.” In Bernstein, L.E., Rohr, F., van Calcar, S. (Eds.) Nutrition Management of Inherited Metabolic Diseases Lessons from Metabolic University, 349–62. Springer, Cham., 2022. https://doi.org/10.1007/978-3-030-94510-7_25.
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    • Korlimarla, Aditi, Sarah Hart, Gail Spiridigliozzi, and Priya Kishnani. “Down syndrome.” In Cassidy and Allanson’s Management of Genetic Syndromes, Fourth Edition, edited by Priya John C. Carey  Agatino Battaglia  David Viskochil  Suzanne B. Cassidy, 355–87. © 2021 John Wiley & Sons, Inc., 2021. https://doi.org/10.1002/9781119432692.ch24.
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    • Kishnani, Priya. “Glycogen storage diseases and other inherited disorders of carbohydrate metabolism (Submitted).” In Harrison’s Principles of Internal Medicine, edited by Priya J. Larry Jameson, Anthony S. Fauci, Dennis L. Kasper, Stephen L. Hauser, Dan L. Longo, Joseph Loscalzo. McGraw-Hill, n.d.
    • Kishnani, Priya. “Disorders of Carbohydrate Metabolism.” In Emery and Rimoin’s Principles and Practice of Medical Genetics and Genomics, edited by Priya Reed Pyeritz Bruce Korf Wayne Grody. Elsevier, Academic Press 2021, n.d.
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  • Digital Publications

    • Korlimarla, Aditi, and Priya S. Kishnani. “Pompe disease.” In: Roos RP, Editor-in-Chief. MedLink Neurology. San Diego: MedLink LLC., December 21, 2021.
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    • Korlimarla, Aditi, and Priya Kishnani. “Pompe disease.” MedLink Neurology. MedLink Corporation, San Diego, October 1, 2020.
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    • Kishnani, Priya. “Pompe disease.” MedLink Neurology, MedLink Corporation, San Diego, February 1, 2018.
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  • Conference Papers

    • Korlimarla, Aditi, Walter Wiggins, Michael Malinzak, James M. Provenzale, and Priya S. Kishnani. “Seizures in infantile Pompe disease: Expanding our understanding of the clinical spectrum.” In Molecular Genetics and Metabolism, 135:S68–S68. Elsevier BV, 2022. https://doi.org/10.1016/j.ymgme.2021.11.170.
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    • Murala, Sireesha, Aditi Korlimarla, Steven Chen, and Priya S. Kishnani. “Diffusion tensor imaging (DTI) findings in children with Pompe disease: Insights into white matter hyperintensities from a longitudinal study.” In Molecular Genetics and Metabolism, 135:S87–S87. Elsevier BV, 2022. https://doi.org/10.1016/j.ymgme.2021.11.224.
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    • Korlimarla, Aditi, Steven Chen, Stephanie L. Austin, James M. Provenzale, and Priya S. Kishnani. “A new look at an old disease: Is Pompe disease a neuromuscular disorder with CNS involvement?” In Molecular Genetics and Metabolism, 129:S92–S92. Elsevier BV, 2020. https://doi.org/10.1016/j.ymgme.2019.11.230.
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    • Korlimarla, Aditi, Ela Stefartescu, Stephanie Austin, Steven Chen, James M. Provenzale, and Priya S. Kishnani. “Quantitative evaluation of white matter hyperintensities in CNS in children with Pompe disease.” In Molecular Genetics and Metabolism, 126:309–309. Elsevier, 2019.
       Link to Item
    • Korlimarla, Aditi, Ela Stefanescu, Stephanie Austin, Steven Chen, James M. Provenzale, and Priya S. Kishnani. “Quantitative evaluation of white matter hyperintensities in the central nervous system in infantile Pompe disease.” In Molecular Genetics and Metabolism, 126:S87–S87. Elsevier BV, 2019. https://doi.org/10.1016/j.ymgme.2018.12.214.
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• Teaching & Mentoring
• 

  Advising & Mentoring

  • 1. Neelam Makhijani, MD: post doctoral research associate, Duke University. Project: Newborn screening in infants with late-onset Pompe disease
    2. Sireesha Murala, MBBS: post doctoral research associate, Duke university. Project: Neurological manifestations in lysosomal storage diseases
    3. Shelly Goombar, PhD: post doc research associate, Duke University. Advice on career pathways for an early career scientist and medical writing
    4. Anna Paschal: Medical student, Duke University. Project: Understanding the natural history of glycogen storage diseases. Mentoring to provide better insight on research study design and methodology for the Masters thesis
    5. Research mentor to undergraduate students, medical students, and clinical post doctoral research associates to orient them to various research activities and responsibilities within the division while maintaining research integrity and to troubleshoot problems during different phases of the research studies
• 

  Teaching Activities

  • Nov 2020: Central nervous system involvement in GSD II (Educational training program for medical students, residents and fellows, genetic counselors as a part of the Medical Education and Awareness Program for Rare Genetic and Metabolic Diseases)
    
    Sept-Nov 2021: Workshop on Scientific/medical writing (4-part series conducted for post docs) 
    
    Nov-Dec 2021: Workshop on Dissecting the world of Publications (3-part series conducted for post docs)
    
    
    
    
    
• Scholarly, Clinical, & Service Activities
• 

  Presentations & Appearances

  • Medical genetics - career pathway for students in STEAM. Arya Math Academy. May 2021  2021
  • Gastrointestinal manifestations in adult patients with late-onset Pompe disease . Annual Pompe Adult Patients meeting. Duke medical genetics. March 2021  2021
  • Neurology in Pompe disease. Annual Pompe Pediatric Meeting. Duke medical genetics. April 2019  2019

Some information on this profile has been compiled automatically from Duke databases and external sources. (Our About page explains how this works.) If you see a problem with the information, please write to Scholars@Duke and let us know. We will reply promptly.