| An emerging phenotype of central nervous system involvement in Pompe disease: from bench to bedside and beyond A Korlimarla, JA Lim, PS Kishnani, B Sun Annals of translational medicine 7 (13), 2019 | 51 | 2019 |
| Novel approaches to quantify CNS involvement in children with Pompe disease A Korlimarla, GA Spiridigliozzi, K Crisp, M Herbert, S Chen, M Malinzak, ... Neurology 95 (6), e718-e732, 2020 | 18 | 2020 |
| New Insights into Gastrointestinal Involvement in Late-Onset Pompe Disease: Lessons Learned from Bench and Bedside A Korlimarla, JA Lim, P McIntosh, K Zimmerman, BD Sun, PS Kishnani Journal of clinical medicine 10 (15), 3395, 2021 | 11 | 2021 |
| Down Syndrome A Korlimarla, SJ Hart, GA Spiridigliozzi, PS Kishnani Cassidy and Allanson's Management of Genetic Syndromes, 355-387, 2021 | 11 | 2021 |
| Disorders of carbohydrate metabolism PS Kishnani, YT Chen Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics …, 2021 | 10 | 2021 |
| Behavioral, social and school functioning in children with Pompe disease A Korlimarla, ... Molecular Genetics and Metabolism Reports 25, Article 100635, 2020 | 10 | 2020 |
| Assessment of dysphonia in children with Pompe disease using auditory-perceptual and acoustic/physiologic methods KD Crisp, AT Neel, S Amarasekara, J Marcus, G Nichting, A Korlimarla, ... Journal of clinical medicine 10 (16), 3617, 2021 | 7 | 2021 |
| Glycogen Storage Diseases A Korlimarla, R Gibson, PS Kishnani Nutrition Management of Inherited Metabolic Diseases: Lessons from Metabolic …, 2022 | 2 | 2022 |
| Severe CNS involvement in a subset of long-term treated children with infantile-onset Pompe disease D Kenney-Jung, A Korlimarla, GA Spiridigliozzi, W Wiggins, M Malinzak, ... Molecular Genetics and Metabolism 141 (2), 108119, 2024 | 1 | 2024 |
| Pompe disease PS Kishnani, A Korlimarla Medlink Neurology [Internet], 2020 | 1 | 2020 |
| (Abstract) Quantitative evaluation of white matter hyperintensities in the central nervous system in infantile Pompe disease A Korlimarla, E Stefanescu, S Austin, S Chen, JM Provenzale, ... Abstracts/Molecular Genetics and Metabolism 126, S17-S156, 2019 | 1* | 2019 |
| Hepatic manifestations in glycogen storage disease type III A Korlimarla, S Austin, B Sun, P Kishnani Current Pathobiology Reports 6, 233-240, 2018 | 1 | 2018 |
| Pompe disease AK Priya Kishnani https://www.medlink.com/articles/pompe-disease, Digital, 2021 | | 2021 |
| (Abstract) New insights into GI manifestations in late-onset Pompe disease: Lessons from the bench and bedside A Korlimarla, JA Lim, P McIntosh, B Sun, PS Kishnani Molecular Genetics and Metabolism 132 (2), S58-S59, 2021 | | 2021 |
| Diffusion tensor imaging (DTI) findings in children with Pompe disease: Insights into white matter hyperintensities from a longitudinal study S Muralaa, A Korlimarlaa, S Chenb, PS Kishnania Abstracts/Molecular Genetics and Metabolism 135, S15-S132, 2021 | | 2021 |
| Seizures in infantile Pompe disease: Expanding our understanding of the clinical spectrum A Korlimarla, W Wiggins, M Malinzak, JM Provenzale, PS Kishnani Abstracts/Molecular Genetics and Metabolism 135, S15-S132, 2021 | | 2021 |
| Pompe disease A Korlimarla, P Kishnani Available at https://www.medlink.com/article/pompe_disease . Roos RP, Editor …, 2020 | | 2020 |
| Pompe disease AK Priya S, Kishnani Medlink Neurology [Internet], 2020 | | 2020 |
| (Abstract) A new look at an old disease: Is Pompe disease a neuromuscular disorder with CNS involvement? A Korlimarla, S Chen, SL Austin, JM Provenzale, PS Kishnani Molecular Genetics and Metabolism 129 (2), S92, 2020 | | 2020 |
Mrudu HerbertUniversity of Kentucky, LexingtonVerified email at mail.harvard.edu
