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.

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.

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.

Sharma S, Kaushik JS, Srivastava K, Goswami JN, Sahu JK, Vinayan KP, Mittal R; Association of Child Neurology – Indian Epilepsy Society Expert Committee. Association of Child Neurology (AOCN) - Indian Epilepsy Society (IES) Consensus Guidelines for the Diagnosis and Management of West Syndrome. Indian Pediatr. 2021 Jan 15;58(1):54-66. PMID: 33452776. Link

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.

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.

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.

Sharma S, Kaushik JS, Srivastava K, Goswami JN, Sahu JK, Vinayan KP, Mittal R; Association of Child Neurology – Indian Epilepsy Society Expert Committee. Association of Child Neurology (AOCN) - Indian Epilepsy Society (IES) Consensus Guidelines for the Diagnosis and Management of West Syndrome. Indian Pediatr. 2021 Jan 15;58(1):54-66. PMID: 33452776. Link

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.

Biswas A, Varman M, Gunturi A, Yoganathan S, Gibikote S. Teaching NeuroImages: Acute necrotizing encephalopathy of childhood: Neuroimaging findings. Neurology. 2018 Jan 9;90(2):e177-e178. doi: 10.1212/WNL.0000000000004800. PMID: 29311376.

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

Abraham SSC, Yoganathan S, Koshy B, Oommen SP, Simon A, Mathai S, Korula S, Mathew L, Sathishkumar D, Jasper A, George R, Danda S. Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinent. Eur J Med Genet. 2021 Sep;64(9):104291. doi: 10.1016/j.ejmg.2021.104291. Epub 2021 Jul 22. PMID: 34303877.

Kohli S, Pasangulapati SB, Yoganathan S, Rynjah GL, Prabhakar AT, Aaron S, Alexander M, Mathew V. Study of Refractory Status Epilepticus from a Tertiary Care Center. Ann Indian Acad Neurol. 2017 Apr-Jun;20(2):116-121. doi: 10.4103/aian.AIAN_385_16. PMID: 28615895; PMCID: PMC5470165.

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. Link

Santhanam I, Yoganathan S, Sivakumar VA, Ramakrishnamurugan R, Sathish S, Thandavarayan M. Predictors of Outcome in Children with Status Epilepticus during Resuscitation in Pediatric Emergency Department: A Retrospective Observational Study. Ann Indian Acad Neurol. 2017 Apr-Jun;20(2):142-148. doi: 10.4103/aian.AIAN_369_16. PMID: 28615900; PMCID: PMC5470151.

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.

Malik P, Bidkar SU, Yoganathan S, Mathai S, Danda S, Koshy B. Imaging findings in TRPM6-Related hypomagnesemia with secondary hypocalcemia. Ann Indian Acad Neurol. 2021 Mar-Apr;24(2):247-248. doi: 10.4103/aian.AIAN_243_20. Epub 2021 Apr 28. PMID: 34220071; PMCID: PMC8232497.

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.

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. Link

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.

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.

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.

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.

Joy P, Yoganathan S, Korula S, Abraham SSC, Barney AM, Walter VM, Gibikote S, Danda S. Ghosal hematodiaphyseal dysplasia and response to corticosteroid therapy. Am J Med Genet A. 2021 Feb;185(2):596-599. doi: 10.1002/ajmg.a.61961. Epub 2020 Nov 13. PMID: 33185009. Link

Korula S, Yoganathan S, Peter J, Chandran M, Christudass CS, Danda S. Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic Disorder. Ann Indian Acad Neurol. 2022 Sep-Oct;25(5):983-985. doi: 10.4103/aian.aian_370_22. Epub 2022 Oct 31. PMID: 36561017; PMCID: PMC9764879.

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.

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. Link

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. Link

Srinivasaraghavan R, Jagadeesh A, Yoganathan S, Mathai S, Oommen SP. Unusual Presentation of Adrenal Hypoplasia Congenita. Indian J Pediatr. 2020 Oct;87(10):865-866. doi: 10.1007/s12098-020-03239-6. Epub 2020 Jul 9. PMID: 32643053.

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.

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. Link

Kaushik JS, Sondhi V, Yoganathan S, Dubey R, Sharma S, Vinayan KP, Gupta P, Mittal R; For AOCN Expert Committee. Association of Child Neurology (AOCN) Consensus Statement on the Diagnosis and Management of Febrile Seizures. Indian Pediatr. 2022 Apr 15;59(4):300-306. Epub 2021 Dec 10. PMID: 34894120. Link

Abraham SSC, Yoganathan S, Koshy B, Oommen SP, Simon A, Mathai S, Korula S, Mathew L, Sathishkumar D, Jasper A, George R, Danda S. Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinent. Eur J Med Genet. 2021 Sep;64(9):104291. doi: 10.1016/j.ejmg.2021.104291. Epub 2021 Jul 22. PMID: 34303877.

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. Link

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. Link

Srinivasaraghavan R, Sharma S, Kratz L, Malik P, Yoganathan S, Danda S, Oommen SP. Child with D-2-Hydroxyglutaric Aciduria Type II: A Rare Neurometabolic Disorder. Ann Indian Acad Neurol. 2021 Nov-Dec;24(6):933-934. doi: 10.4103/aian.AIAN_231_20. Epub 2021 Dec 17. PMID: 35359529; PMCID: PMC8965948.

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.

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.

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.

Biswas A, Varman M, Yoganathan S, Subhash PK, Mani S. Teaching NeuroImages: Autosomal recessive spastic ataxia of Charlevoix-Saguenay: Typical MRI findings. Neurology. 2018 Apr 3;90(14):e1271-e1272. doi: 10.1212/WNL.0000000000005252. PMID: 29610238.

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. Link

Whitney R, Komar M, Yoganathan S, Costain G, Jain P. Epilepsy in KBG Syndrome: Report of Additional Cases. Pediatr Neurol. 2024 Feb;151:138-142. doi: 10.1016/j.pediatrneurol.2023.12.006. Epub 2023 Dec 14. PMID: 38157719.

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.

Nagarajan B, Gowda VK, Yoganathan S, Sharawat IK, Srivastava K, Vora N, Badheka R, Danda S, Kalane U, Kaur A, Madaan P, Mehta S, Negi S, Panda PK, Rajadhyaksha S, Saini AG, Saini L, Shah S, Srinivasan VM, Suthar R, Thomas M, Vyas S, Sankhyan N, Sahu JK. Landscape of genetic infantile epileptic spasms syndrome-A multicenter cohort of 124 children from India. Epilepsia Open. 2023 Dec;8(4):1383-1404. doi: 10.1002/epi4.12811. Epub 2023 Aug 25. PMID: 37583270; PMCID: PMC10690684.