Muthusamy K, Thomas M, Yoganathan S, Sudhakar SV. Clinical Profile, Prognostic Indicators, and Therapeutic Outcomes of Pediatric Opsoclonus-Myoclonus-Ataxia Syndrome: A Single-Center Experience from South India. Ann Indian Acad Neurol. 2019 Jul-Sep;22(3):295-301. doi: 10.4103/aian.AIAN_101_18. PMID: 31359941; PMCID: PMC6613420.

Muthusamy K, Sudhakar SV, Thomas M, Yoganathan S, Christudass CS, Chandran M, Panwala H, Gibikote S. Revisiting magnetic resonance imaging pattern of Krabbe disease - Lessons from an Indian cohort. J Clin Imaging Sci. 2019 May 24;9:25. doi: 10.25259/JCIS-18-2019. PMID: 31448176; PMCID: PMC6702867.

Kapoor N, Cherian KE, Sajith KG, Thomas M, Eapen CE, Thomas N, Paul TV. Renal Tubular Function, Bone Health and Body Composition in Wilson's Disease: A Cross-Sectional Study from India. Calcif Tissue Int. 2019 Nov;105(5):459-465. doi: 10.1007/s00223-019-00588-z. Epub 2019 Jul 17. PMID: 31317233.

Muthusamy K, Yoganathan S, Thomas MM, Alexander M, Verghese VP. Subacute sclerosing panencephalitis in a child with human immunodeficiency virus (HIV) infection on antiretroviral therapy. Ann Indian Acad Neurol. 2015 Jan-Mar;18(1):96-8. doi: 10.4103/0972-2327.144299. PMID: 25745323; PMCID: PMC4350227.

Aaron S, Alexander M, Moorthy RK, Mani S, Mathew V, Patil AK, Sivadasan A, Nair S, Joseph M, Thomas M, Prabhu K, Joseph BV, Rajshekhar V, Chacko AG. Decompressive craniectomy in cerebral venous thrombosis: a single centre experience. J Neurol Neurosurg Psychiatry. 2013 Sep;84(9):995-1000. doi: 10.1136/jnnp-2012-303356. Epub 2013 Apr 16. PMID: 23591554.

Thakkar P, B P N, Yoganathan S, John JA, Thomas M. Status dystonicus: Diagnosis and management of a rare and challenging entity. J Pediatr Rehabil Med. 2019;12(1):71-74. doi: 10.3233/PRM-170510. PMID: 30883367.

Muthusamy K, Thomas M, Yoganathan S, Sudhakar SV. Clinical Profile, Prognostic Indicators, and Therapeutic Outcomes of Pediatric Opsoclonus-Myoclonus-Ataxia Syndrome: A Single-Center Experience from South India. Ann Indian Acad Neurol. 2019 Jul-Sep;22(3):295-301. doi: 10.4103/aian.AIAN_101_18. PMID: 31359941; PMCID: PMC6613420.

Muthusamy K, Sudhakar SV, Thomas M, Yoganathan S, Christudass CS, Chandran M, Panwala H, Gibikote S. Revisiting magnetic resonance imaging pattern of Krabbe disease - Lessons from an Indian cohort. J Clin Imaging Sci. 2019 May 24;9:25. doi: 10.25259/JCIS-18-2019. PMID: 31448176; PMCID: PMC6702867.

Kapoor N, Cherian KE, Sajith KG, Thomas M, Eapen CE, Thomas N, Paul TV. Renal Tubular Function, Bone Health and Body Composition in Wilson's Disease: A Cross-Sectional Study from India. Calcif Tissue Int. 2019 Nov;105(5):459-465. doi: 10.1007/s00223-019-00588-z. Epub 2019 Jul 17. PMID: 31317233.

Muthusamy K, Yoganathan S, Thomas MM, Alexander M, Verghese VP. Subacute sclerosing panencephalitis in a child with human immunodeficiency virus (HIV) infection on antiretroviral therapy. Ann Indian Acad Neurol. 2015 Jan-Mar;18(1):96-8. doi: 10.4103/0972-2327.144299. PMID: 25745323; PMCID: PMC4350227.

Aaron S, Alexander M, Moorthy RK, Mani S, Mathew V, Patil AK, Sivadasan A, Nair S, Joseph M, Thomas M, Prabhu K, Joseph BV, Rajshekhar V, Chacko AG. Decompressive craniectomy in cerebral venous thrombosis: a single centre experience. J Neurol Neurosurg Psychiatry. 2013 Sep;84(9):995-1000. doi: 10.1136/jnnp-2012-303356. Epub 2013 Apr 16. PMID: 23591554.

Thakkar P, B P N, Yoganathan S, John JA, Thomas M. Status dystonicus: Diagnosis and management of a rare and challenging entity. J Pediatr Rehabil Med. 2019;12(1):71-74. doi: 10.3233/PRM-170510. PMID: 30883367.

Valmiki RR, Venkatesalu S, Chacko AG, Prabhu K, Thomas MM, Mathew V, Yoganathan S, Muthusamy K, Chacko G, Vanjare HA, Krothapalli SB Phosphoproteomic analysis reveals Akt isoform-specific regulation of cytoskeleton proteins in human temporal lobe epilepsy with hippocampal sclerosis. Neurochem Int. 2020 Mar;134:104654. doi: 10.1016/j.neuint.2019.104654. Epub 2019 Dec 27. PMID: 31884041.

Yoganathan S, Mariappan R, Sudhakar SV, Mani SE, Mathew V, Thomas M, Aboobacker FN. An Unusual Cause of Chronic Headache in an Adolescent Boy: A Case Report . Neuropediatrics. 2019 Dec;50(6):395-399. doi: 10.1055/s-0039-1694974. Epub 2019 Sep 17. PMID: 31529425.

Job A, Naina P, Syed KA, Thomas M, John M, Varghese AM. Validation of a drooling questionnaire in Indian children with cerebral palsy. Int J Pediatr Otorhinolaryngol. 2018 Sep;112:55-60. oi: 10.1016/j.ijporl.2018.06.029. Epub 2018 Jun 19. PMID: 30055740

Selvam P, Arunachal G, Danda S, Chapla A, Sivadasan A, Alexander M, Thomas MM, Thomas NJ. Congenital Myasthenic Syndrome: Spectrum of Mutations in an Indian Cohort. J Clin Neuromuscul Dis. 2018 Sep;20(1):14-27. doi: 10.1097/CND.0000000000000222. PMID: 30124556.

Varala S, George R, Mathew L, Russell P, Koshy B, Oommen SP, Thomas M, Muthusamy K, Yoganathan S, Jeyaseelan L, Muliyil J. The Diagnostic Value of Congenital and Nevoid Cutaneous Lesions Associated with Autism Spectrum Disorders in Indian Children- A Case-Control Study. Indian Dermatol Online J. 2021 Jan 16;12(1):84-89. doi: 10.4103/idoj.IDOJ_275_20. PMID: 33768027; PMCID: PMC7982006

Naik GS, Kodagali R, Mathew BS, Thomas M, Prabha R, Mathew V, Fleming DH. Therapeutic Drug Monitoring of Levetiracetam and Lamotrigine: Is There a Need? Ther Drug Monit. 2015 Aug;37(4):437-44. doi: 10.1097/FTD.0000000000000158. PMID: 25478905.

Yoganathan S, Sudhakar S, Thomas M, Kumar Dutta A, Danda S, Chandran M. Novel Imaging Finding and Novel Mutation in an Infant with Molybdenum Cofactor Deficiency, a Mimicker of Hypoxic-Ischaemic Encephalopathy. Iran J Child Neurol. 2018 Spring;12(2):107-112. PMID: 29696052; PMCID: PMC5904745.

Yoganathan S, Kumar M, Sudhakar S, Malhotra M, Thomas M. Recurrent Painful Ophthalmoplegic Neuropathy: A Cause of Headache. Indian J Pediatr. 2021 Aug 3. doi: 10.1007/s12098-021-03886-3. Epub ahead of print. PMID: 34342792.

Yoganathan S, Srinivasaraghavan R, Chandran M, Kratz L, Koshy B, Sudhakar SV, Arunachal G, Thomas M, Danda S. Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental Disorder. Ann Indian Acad Neurol. 2021 Mar-Apr;24(2):261-264. doi: 10.4103/aian.AIAN_361_20. Epub 2021 Apr 28. PMID: 34220079; PMCID: PMC8232503.

Jena SS, Alexander M, Aaron S, Mathew V, Thomas MM, Patil AK, Sivadasan A, Muthusamy K, Mani S, Rebekah JG. Natural history of multiple sclerosis from the Indian perspective: Experience from a tertiary care hospital. Neurol India. 2015 Nov-Dec;63(6):866-73. doi: 10.4103/0028-3886.170079. PMID: 26588619.

Yoganathan S, Sudhakar SV, Thomas M, Dutta AK, Danda S. "Eye of tiger sign" mimic in an adolescent boy with mitochondrial membrane protein associated neurodegeneration (MPAN). Brain Dev. 2016 May;38(5):516-9. doi: 10.1016/j.braindev.2015.10.017. Epub 2015 Nov 18. PMID: 26602591.

Yoganathan S, Arunachal G, Kratz L, Varman M, Sudhakar SV, Oommen SP, Jain S, Thomas M, Babuji M. Guanidinoacetate Methyltransferase (GAMT) Deficiency, A Cerebral Creatine Deficiency Syndrome: A Rare Treatable Metabolic Disorder. Ann Indian Acad Neurol. 2020 May-Jun;23(3):419-421. doi: 10.4103/aian.AIAN_172_19. Epub 2020 Jan 3. PMID: 32606564; PMCID: PMC7313585.

Kamath V, Yoganathan S, Thomas MM, Gowri M, Chacko MP. Utility of Chromosomal Microarray in Children with Unexplained Developmental Delay/Intellectual Disability. Fetal Pediatr Pathol. 2022 Apr;41(2):208-218. doi: 10.1080/15513815.2020.1791292. Epub 2020 Jul 23. PMID: 32701375.

Kumar M, Yoganathan S, P MT, Thomas MM. Never Miss Sleep Disorder in Children with Drop Attacks. Indian J Pediatr. 2022 Jan;89(1):95. doi: 10.1007/s12098-021-03856-9. Epub 2021 Sep 1. PMID: 34468940.

Yoganathan S, Thomas MM, Mathai S, Ghosh U. Neuroregression as an initial manifestation in a toddler with acquired pernicious anaemia. BMJ Case Rep. 2015 Dec 17;2015:bcr2015213540. doi: 10.1136/bcr-2015-213540. PMID: 26678841; PMCID: PMC4691932.

Joseph E, Sureka J, Gibikote S, Aaron S, Thomas MM. Megalencephalic leukoencephalopathy with subcortical cysts in an adult. Acta Neurol Belg. 2009 Mar;109(1):53-4. PMID: 19402576.

Yoganathan S, Arunachal G, Gowda VK, Vinayan KP, Thomas M, Whitney R, Jain P. NTRK2-related developmental and epileptic encephalopathy: Report of 5 new cases. Seizure. 2021 Nov;92:52-55. doi: 10.1016/j.seizure.2021.08.008. Epub 2021 Aug 18. PMID: 34425480.

Danda S, Datar C, Kher A, Deshpande T, Thomas MM, Oommen SP. First reported cases with Xia-Gibbs syndrome from India harboring novel variants in AHDC1. Am J Med Genet A. 2022 Aug;188(8):2501-2504. doi: 10.1002/ajmg.a.62844. Epub 2022 May 21. PMID: 35596688.

Kotambail A, Selvam P, Muthusamy K, Thomas M, Sudhakar SV, Ghati C, Danda S, Arunachal G. Clustering of Juvenile Canavan disease in an Indian community due to population bottleneck and isolation: genomic signatures of a founder event. Eur J Hum Genet. 2023 Jan;31(1):73-80. doi: 10.1038/s41431-022-01198-4. Epub 2022 Oct 7. PMID: 36202930; PMCID: PMC9823096.

Yoganathan S, Sudhakar SV, Arunachal G, Thomas M, Subramanian A, George R, Danda S. Menkes disease and response to copper histidine: An Indian case series Ann Indian Acad Neurol. 2017 Jan-Mar;20(1):62-68. doi: 10.4103/0972-2327.199907. PMID: 28298846; PMCID: PMC5341272.

Yoganathan S, Kumar M, Sushma L, Danda S, Thomas M. An Inherited Cause of Stroke Mimic in a Toddler. Indian J Pediatr. 2021 Sep 1. doi: 10.1007/s12098-021-03904-4. Epub ahead of print. PMID: 34468936.

Bharathi NK, Thomas MM, Yoganathan S, Chandran M, Aaron R, Danda S. Phenotypic Pleiotropy in Arginase Deficiency: A Single Center Cohort. Ann Indian Acad Neurol. 2022 Nov-Dec;25(6):1104-1108. doi: 10.4103/aian.aian_612_22. Epub 2022 Dec 3. PMID: 36911443; PMCID: PMC9996474.

Sathishkumar D, George R, Irodi A, Thomas M. PHACES syndrome with moyamoya vasculopathy - a case report. Dermatol Online J. 2013 Aug 15;19(8):19271. PMID: 24021449.

Malik P, Yoganathan S, Danda S, Thomas M. Unusual MRI findings in 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency. Neuropediatrics. 2022 Feb 22. doi: 10.1055/a-1779-4234. Epub ahead of print. PMID: 35193149.

Das S, Thomas M, Yoganathan S, Muthusamy K, Barney AM, A SSC, Dutta AK, A R, Mohan S, Danda S. Exploration of clinical and genetic findings in Ataxia-Telangiectasia (AT) patients from the Indian subcontinent. Eur J Med Genet. 2023 Jun;66(6):104766. doi: 10.1016/j.ejmg.2023.104766. Epub 2023 Apr 17. PMID: 37075885.

Garg D, Yoganathan S, Shamim U, Mankad K, Gulati P, Bonifati V, Botre A, Kalane U, Saini AG, Sankhyan N, Srivastava K, Gowda VK, Juneja M, Kamate M, Padmanabha H, Panigrahi D, Pachapure S, Udani V, Kumar A, Pandey S, Thomas M, Danda S, Iqbalahmed SA, Subramanian A, Pemde H, Singh V, Faruq M, Sharma S. Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children. Mov Disord Clin Pract. 2022 Aug 12;9(7):886-899. doi: 10.1002/mdc3.13516. PMID: 36247901; PMCID: PMC9547147.

Kumar M, Yoganathan S, Todari S, Suresh P, Chandran M, Danda S, Mathew LG, Koshy B, Thomas M. Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations. Ann Indian Acad Neurol. 2022 Nov-Dec;25(6):1238-1241. doi: 10.4103/aian.aian_1118_21. Epub 2022 Dec 3. PMID: 36911455; PMCID: PMC9996535.

Malik P, Yoganathan S, Danda S, Thomas M. Unusual Magnetic Resonance Imaging Findings in 3-Hydroxy-3-Methylglutaryl-Coenzyme A Lyase Deficiency. Neuropediatrics. 2022 Dec;53(6):445-447. doi: 10.1055/a-1779-4234. Epub 2022 Feb 22. PMID: 35193149.

Kumar M, Yoganathan S, P MT, Thomas MM. Never Miss Sleep Disorder in Children with Drop Attacks. Indian J Pediatr. 2021 Sep 1. doi: 10.1007/s12098-021-03856-9. Epub ahead of print. PMID: 34468940.

Yoganathan S, Sharma S, Varman M, Malhotra M, Chandran M, Arunachal G, Thomas M. A Treatable Cause of Intellectual Disability and Autism in a Young Child. Indian J Pediatr. 2020 Oct;87(10):850-851. doi: 10.1007/s12098-020-03225-y. Epub 2020 Mar 24. PMID: 32207074.

Muthusamy K, Sudhakar SV, Yoganathan S, Thomas MM, Alexander M. Hypomyelination, Hypodontia, Hypogonadotropic Hypogonadism (4H) Syndrome With Vertebral Anomalies: A Novel Association. J Child Neurol. 2015 Jun;30(7):937-41. doi: 10.1177/0883073814541470. Epub 2014 Sep 11. PMID: 25213661.

Yoganathan S, Kumar M, Sharma S, Patel S, Danda S, Thomas M. SGCE Myoclonus-Dystonia: An Inherited Movement Disorder. Neurology. 2022 Feb 15;98(7):289. doi: 10.1212/WNL.0000000000013209. Epub 2021 Dec 14. PMID: 34906973.

Danda S, Datar C, Kher A, Deshpande T, Thomas MM, Oommen SP. First reported cases with Xia-Gibbs syndrome from India harboring novel variants in AHDC1. Am J Med Genet A. 2022 Aug;188(8):2501-2504. doi: 10.1002/ajmg.a.62844. Epub 2022 May 21. PMID: 35596688.

Yoganathan S, Arunachal G, Kratz L, Varman M, Thomas M, Sudhakar SV, Oommen SP, Danda S. Metabolic Or Ischemic Stroke in Succinic Semi-Aldehyde Dehydrogenase Deficiency Due to the Homozygous Variant c. 1343 + 1_1343 + 3delGTAinsTT in ALDH5A1. Ann Indian Acad Neurol. 2021 Mar-Apr;24(2):259-261. doi: 10.4103/aian.AIAN_360_20. Epub 2021 Apr 28. PMID: 34220078; PMCID: PMC8232515.

Yoganathan S, Kumar M, Sharma S, Patel S, Danda S, Thomas M. SGCE Myoclonus-Dystonia: An Inherited Movement Disorder. Neurology. 2021 Dec 14:10.1212/WNL.0000000000013209. doi: 10.1212/WNL.0000000000013209. Epub ahead of print. PMID: 34906973.

Yoganathan S, Sudhakar SV, Priyambada L, Thomas M. Stroke in a Child with Dengue Encephalopathy. Ann Indian Acad Neurol. 2017 Jul-Sep;20(3):329-331. doi: 10.4103/aian.AIAN_504_16. PMID: 28904475; PMCID: PMC5586138.

Yoganathan S, Kumar M, Sudhakar S, Malhotra M, Thomas M. Recurrent Painful Ophthalmoplegic Neuropathy: A Cause of Headache. Indian J Pediatr. 2022 Apr;89(4):407-408. doi: 10.1007/s12098-021-03886-3. Epub 2021 Aug 3. PMID: 34342792.

Yoganathan S, Kumar M, Sushma L, Danda S, Thomas M. An Inherited Cause of Stroke Mimic in a Toddler. Indian J Pediatr. 2022 Jan;89(1):98. doi: 10.1007/s12098-021-03904-4. Epub 2021 Sep 1. PMID: 34468936.

Yoganathan S, Bhasin H, Garg D, Malik P, Saini AG, Chandran M, Korula S, Arunachal G, Danda S, Thomas M, Oommen SP, Sharma S. Childhood Neurological Disorders With Hyperhomocystinemia: A Case-Based Review. Pediatr Neurol. 2023 Sep;146:26-30. doi: 10.1016/j.pediatrneurol.2023.06.003. Epub 2023 Jun 13. PMID: 37413720.

Sindhu KN, Srinivasan M, Moses PD, Thomas M, John J, Rose W. Subsultus Tendinum in a Child with Typhoid Fever. Indian Pediatr. 2020 Apr 15;57(4):374-375. PMID: 32284487.

Abraham AP, Thomas MM, Mathew V, Muthusamy K, Yoganathan S, Jonathan GE, Prabhu K, Daniel RT, Chacko AG EEG lateralization and seizure outcome following peri-insular hemispherotomy for pediatric hemispheric epilepsy. Childs Nerv Syst. 2019 Jul;35(7):1189-1195. doi: 10.1007/s00381-019-04067-6. Epub 2019 Jan 30. PMID: 30701299.

Yoganathan S, Arunachal G, Kratz L, Varman M, Sudhakar SV, Oommen SP, Jain S, Thomas M, Babuji M. Guanidinoacetate Methyltransferase (GAMT) Deficiency, A Cerebral Creatine Deficiency Syndrome: A Rare Treatable Metabolic Disorder. Ann Indian Acad Neurol. 2020 May-Jun;23(3):419-421. doi: 10.4103/aian.AIAN_172_19. Epub 2020 Jan 3. PMID: 32606564; PMCID: PMC7313585.

Nair S, Jacob J, Aaron S, Thomas M, Joseph M, Alexander M. Pulmonary distress following attempted suicidal hanging. Indian J Med Sci. 2009 Feb;63(2):53-7. PMID: 19359767.

Joshi SP, Thomas M, Yoganathan S, Danda S, Chandran M, Jasper A. Clinico-Etiological Spectrum and Functional Outcomes of Children with Pre-Status Dystonicus and Status Dystonicus (SD): A Descriptive Study. Ann Indian Acad Neurol. 2023 May-Jun;26(3):268-274. doi: 10.4103/aian.aian_660_22. Epub 2023 Jun 15. PMID: 37538432; PMCID: PMC10394458.

John D, Thomas M, Jacob P. Neurotrophic keratitis and congenital insensitivity to pain with anhidrosis--a case report with 10-year follow-up. Cornea. 2011 Jan;30(1):100-2. doi: 10.1097/ICO.0b013e3181e458e4. PMID: 20847675.

Kumar M, Murugan TP, Lionel AP, Thomas MM, Mannam P, Yoganathan S. Management of Children and Adolescents with Wilson Disease and Neurological Worsening Following D-Penicillamine Therapy: A Single Centre Experience. Ann Indian Acad Neurol. 2022 Jul-Aug;25(4):698-702. doi: 10.4103/aian.aian_519_21. Epub 2022 Sep 9. PMID: 36211139; PMCID: PMC9540946.

Yoganathan S, Kumar M, Malhotra M, Joy P, Danda S, Thomas M, David KS, Jasper A, Selvin SST. Eye signs in a child with ROBO3 gene mutation. Indian J Ophthalmol. 2022 Jul;70(7):2643-2644. doi: 10.4103/ijo.IJO_2065_21. PMID: 35791185; PMCID: PMC9426051.

Yoganathan S, Kumar M, John D, Danda S, Oommen SP, Umakant SB, Thomas M. Oculodigital Sign: A Clinical Clue for Diagnosis. Ann Indian Acad Neurol. 2022 May-Jun;25(3):560-561. doi: 10.4103/aian.aian_755_21. Epub 2022 May 3. PMID: 35936593; PMCID: PMC9350766.

Yoganathan S, Srinivasaraghavan R, Kumar M, Kratz L, Mular S, Sudhakar SV, Malik P, Chandran M, Thomas M, Danda S. Fumaric Aciduria: A Rare Cause of Refractory Epilepsy. Ann Indian Acad Neurol. 2022 Jul-Aug;25(4):738-740. doi: 10.4103/aian.aian_47_22. Epub 2022 Sep 9. PMID: 36211164; PMCID: PMC9540961.

Yoganathan S, Srinivasaraghavan R, Chandran M, Kratz L, Koshy B, Sudhakar SV, Arunachal G, Thomas M, Danda S. Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental Disorder. Ann Indian Acad Neurol. 2021 Mar-Apr;24(2):261-264. doi: 10.4103/aian.AIAN_361_20. Epub 2021 Apr 28. PMID: 34220079; PMCID: PMC8232503.

Jain S, Muthusamy K, Bernice TS, Pansuriya H, Punnen A, Kumar S, Thomas MM. A Rare Treatable and Under Recognized Cause of Recurrent Convexity Subarachnoid Hemorrhage: Lupus Anticoagulant Hypoprothombinemia Syndrome. Ann Indian Acad Neurol. 2021 Nov-Dec;24(6):986-989. doi: 10.4103/aian.AIAN_804_20. Epub 2021 Apr 14. PMID: 35359554; PMCID: PMC8965963.

John D, Muthusamy K, Bandla B, Sudhakar SV, Thomas M. Ocular Features and Visual Outcome in Children with Moyamoya Disease and Moyamoya Syndrome: A Case Series. J Clin Diagn Res. 2016 May;10(5):NR01-4. doi: 10.7860/JCDR/2016/19153.7744. Epub 2016 May 1. PMID: 27437259; PMCID: PMC4948435.

Muthusamy K, Ekbote AV, Thomas MM, Aaron S, Mathew V, Patil AB, Sivadasan A, Prabhakar AT, Yoganathan S, Alexander M. Biotin thiamine responsive basal ganglia disease-A potentially treatable inborn error of metabolism. Neurol India. 2016 Nov-Dec;64(6):1328-1331. doi: 10.4103/0028-3886.193797. PMID: 27841215.

Benjamin RN, Thomas M, Muthusamy K, Yoganathan S, Mathew V, Chacko AG, Prabhu K, Chacko G. Age-Dependent Reduction in Severity and Discrete Topographical Patterns in Rasmussen Encephalitis: A Link to Cortical Maturation? Pediatr Neurol. 2020 Nov;112:25-33. doi: 10.1016/j.pediatrneurol.2020.07.016. Epub 2020 Aug 11. PMID: 32911260.

Muthusamy K, Thomas MM, George RE, Alexander M, Mani S, Benjamin RN. Siblings with fucosidosis. J Pediatr Neurosci. 2014 May;9(2):156-8. doi: 10.4103/1817-1745.139331. PMID: 25250075; PMCID: PMC4166842.

Koshy G, Varghese RT, Naik D, Asha HS, Thomas N, Seshadri MS, Alexander M, Thomas M, Aaron S, Paul TV. Derangements in bone mineral parameters and bone mineral density in south Indian subjects on antiepileptic medications. Ann Indian Acad Neurol. 2014 Jul;17(3):272-6. doi: 10.4103/0972-2327.138489. PMID: 25221394; PMCID: PMC4162011.

Yoganathan S, Arunachal G, Sudhakar SV, Rajaraman V, Thomas M, Danda S. Beta Propellar Protein-Associated Neurodegeneration: A Rare Cause of Infantile Autistic Regression and Intracranial Calcification. Neuropediatrics. 2016 Apr;47(2):123-7. doi: 10.1055/s-0035-1571189. Epub 2016 Feb 9. PMID: 26859818.

Yoganathan S, Arunachal G, Kratz L, Varman M, Thomas M, Sudhakar SV, Oommen SP, Danda S. Metabolic Stroke: A Novel Presentation in a Child with Succinic Semialdehyde Dehydrogenase Deficiency. Ann Indian Acad Neurol. 2020 Jan-Feb;23(1):113-117. doi: 10.4103/aian.AIAN_213_18. PMID: 32055132; PMCID: PMC7001443.

Yoganathan S, Varman M, Oommen SP, Thomas M. A Tale of Treatable Infantile Neuroregression and Diagnostic Dilemma with Glutaric Aciduria Type I. J Pediatr Neurosci. 2017 Oct-Dec;12(4):356-359. doi: 10.4103/jpn.JPN_35_17. PMID: 29675077; PMCID: PMC5890558.

Yoganathan S, Sudhakar SV, Thomas MM, Yadav VK. A tropical menace of co-infection of Japanese encephalitis and neurocysticercosis in two children. J Pediatr Neurosci. 2016 Apr-Jun;11(2):140-4. doi: 10.4103/1817-1745.187644. PMID: 27606026; PMCID: PMC4991158.

Yoganathan S, Whitney R, Thomas M, Danda S, Chettali AM, Prasad AN, Farhan SMK, AlSowat D, Abukhaled M, Aldhalaan H, Gowda VK, Kinhal UV, Bylappa AY, Konanki R, Lingappa L, Parchuri BM, Appendino JP, Scantlebury MH, Cunningham J, Hadjinicolaou A, El Achkar CM, Kamate M, Menon RN, Jose M, Riordan G, Kannan L, Jain V, Manokaran RK, Chau V, Donner EJ, Costain G, Minassian BA, Jain P. KCTD7-related progressive myoclonic epilepsy: Report of 42 cases and review of literature. Epilepsia. 2024 Jan 17. doi: 10.1111/epi.17880. Epub ahead of print. PMID: 38231304.

Muthusamy K, Sivadasan A, Dixon L, Sudhakar S, Thomas M, Danda S, Wszolek ZK, Wierenga K, Dhamija R, Gavrilova R. Adult-onset leukodystrophies: a practical guide, recent treatment updates, and future directions. Front Neurol. 2023 Jul 26;14:1219324. doi: 10.3389/fneur.2023.1219324. PMID: 37564735; PMCID: PMC10410460.

John R, Chapla A, Chacko G, Yoganathan S, Thomas MM, Thomas N. Response to Letter to the Editor from Finsterer "Diverse Phenotypes of Mitochondrial Disease With Varying Levels of Heteroplasmy". JCEM Case Rep. 2025 Jul 1;3(8):luaf128. doi: 10.1210/jcemcr/luaf128. PMID: 40599483; PMCID: PMC12210230.