Research & Development



    DETAILS OF SCIENTIFIC ARTICLES PUBLISHED

  • M. Iype, N. Melempatt, J. James, S.V. Thomas, A. Anitha, “Hypomethylation of WNT signaling regulator genes in developmental language disorder,” Epigenomics, vol. 16, pp. 137-146, 2024.
  • A. Anitha, I. Thanseem, M. Iype, S.V. Thomas, “Mitochondrial dysfunction in cognitive neurodevelopmental disorders: Cause or effect?” Mitochondrion, vol. 69, pp. 18-32, 2023
  • A. Anitha, M. Banerjee, I. Thanseem, A. Prakash, N. Melempatt, P.S. Sumitha, M. Iype, S.V. Thomas, “Rare pathogenic variants identified in whole exome sequencing of monozygotic twins with autism spectrum disorders,” Pediatric Neurology, vol. 158, pp. 113-123, 2024.
  • K. Kumar, S. Thomas, M.C. Nair, G. Parvathy, M.L. Nisha, S. Anuradha, et al, “Ayurvedic management of presbycusis (Project TOPMAC): Protocol for an exploratory randomized controlled trial,” JMIR Research Protocols, vol. 23, pp. 13:e55089, 2024
  • M.M. Vasu, L. Koshy, S. Ganapathi, P. Jeemon, M. Urulangodi, S. Gopala, P. Greeva, A. Anitha, et al, “Identification of novel endogenous control miRNAs in heart failure for normalization of qPCR data,” International Journal of Biological Macromolecules, vol. 261 (Pt2), pp. 129714, 2024.
  • I. Thanseem, M. Banerjee, N. Melempatt, A. Prakash, M. Iype, A. Anitha,“Comprehensive genetic study of a monozygotic triplet discordant for autism spectrum disorder,” Neurology India, vol. 72, pp. 384-387, 2024
  • Thanseem I, Banerjee M, Melempatt N, Prakash A, Iype M, Anitha A. Comprehensive genetic study of a monozygotic triplet discordant for autism spectrum disorder. Neurol India (Accepted)
  • Anitha A, Thanseem I, Iype M, Thomas SV (2023) Mitochondrial dysfunction in cognitive neurodevelopmental disorders: Cause or effect? Mitochondrion 69: 18-32
  • Indiradevi KP, Suhara EM, Poovathinal SA, Anitha A (2022) Distinguishing cognitive states using electroencephalography local activation and functional connectivity patterns. Biomed Signal Process Control 77: 103742.
  • Mathew V, Srivastava R, Nair AK. Difference in the cognitive profile of children with specific learning disabilities. Santosh Univ J Health Sci. 2022, 8: 48-51
  • Thomas SV, Salim S, Jacob NS, Jose M, Salini RA, Selvaraj S, Gomez TS, Sreedharan H, Jeemon P. Language, intelligence, and educational outcomes of adolescents with antenatal exposure to antiseizure medications: Prospective data from the Kerala Registry of epilepsy and pregnancy. Seizure. 2022 Aug;100:76-81. doi: 10.1016/j.seizure.2022.06.005. Epub 2022 Jun 17. PMID: 35780605.
  • Chandrasekharan SV, Menon RN, Nanda S, Nair JS, Radhakrishnan A, Cherian A, Thomas SV. Does Etiology and Hypsarrhythmia Subtype Influence Outcome in West Syndrome? Challenges Encountered from a Referral Center Perspective. Neurol India. 2022 JanFeb;70(1):188-196. doi: 10.4103/0028-3886.336325. PMID: 35263882.
  • Menon RN, Nambiar PN, Keni RR, Baishya J, Radhakrishnan A, Cherian A, Nampoothiri S, Madhavilatha GK, Kotecha UH, Thomas SV. Drug-resistant ‘Non- Lesional’ Visual Sensitive Epilepsies of Childhood - Electroclinical Phenotype- Genotype Associations. Neurol India. 2021 Nov-Dec;69(6):1701-1705. doi: 10.4103/0028-3886.333508. PMID: 34979672.
  • Rudrabhatla PK, Reghukumar A, Thomas SV. Mucormycosis in COVID-19 patients: predisposing factors, prevention and management. Acta Neurol Belg. 2022 Apr;122(2):273-280. doi: 10.1007/s13760-021-01840-w. Epub 2021 Nov 24. PMID: 34820787; PMCID: PMC8612391.
  • Thomas SV, Jeemon P, Pillai R, Jose M, Lalithakumari AM, Murali S, Sanalkumar A, Salini RA, Pavithran V. Malformation risk of new anti-epileptic drugs in women with epilepsy; observational data from the Kerala registry of epilepsy and pregnancy (KREP). Seizure. 2021 Dec;93:127-132. doi: 10.1016/j.seizure.2021.10.015. Epub 2021 Oct 23. PMID: 34740142.
  • Asranna A, Thomas SV. Metabolic Effects of Anti-Seizure Medications: A Time to Reevaluate Risks? Neurol India. 2021 Jul-Aug;69(4):964-965. doi: 10.4103/0028-3886.325336. PMID: 34507422.
  • Baishya J, Menon RN, Ravish Keni R, Saraf UU, Varma RP, Radhakrishnan A, Cherian A, Thomas SV. Can occurrence of convulsive status epilepticus during video telemetry be predicted? Observations from an epilepsy monitoring unit. Epilepsy Behav. 2021 Oct;123:108252. doi: 10.1016/j.yebeh.2021.108252. Epub 2021 Aug 23. PMID: 34438130.
  • Seshachala BB, Jose M, Lathikakumari AM, Murali S, Kumar AS, Thomas SV. Valproate usage in pregnancy: An audit from the Kerala Registry of Epilepsy and Pregnancy. Epilepsia. 2021 May;62(5):1141-1147. doi: 10.1111/epi.16882. Epub 2021 Mar 29. PMID: 33782943.
  • Anitha A, Poovathinal SA, Viswambharan V, Thanseem I, Iype M, Anoop U, et al. MECP2 Mutations in the Rett Syndrome Patients from South India. Neurol India 2022;70:249-53
  • Swetha Damodharan , Mary Iype , Ayyappan Anitha. Neurodevelopmental genes in photoparoxysmal EEG response. In the conference proceedings of 8th Annual Conference of Cognitive Science (ACCS8)
  • Dr. Nandini Jayachandran, Dr. Immanuel Thomas, Dr. Mary Iype, Dr. Suresh P.A. and Sneha Sebastian Cultural Adaptation of M-CHAT R/F Malayalam version In the conference proceedings of 8th Annual Conference of Cognitive Science (ACCS8)
  • Mary Iype, Mithran OS, AnithaAyyappan, MathewIype “Congenital Muscular Dystrophy Due to POMGNT1 Mutation Presenting As Cardio-embolic Stroke AIAN 2022;25(3):551-3. “DOI:10.4103/aian.aian_944_21
  • James Jesmy, Iype Mary, Surendran Mithran Omana, Anitha Ayyappan, Thomas Sanjeev V. The genetic landscape of polymicrogyria AIAN 2022;25(4):616- 26. DOI:10.4103/aian.aian_97_22
  • Ayyappan A, Thanseem Mohammed, Moinak Banerjee, Nisha Melempatt, Anil Prakash, MuhasinParapurathu, Mary Iype.” Comprehensive Genetic Study of a Monozygotic Triplet Discordant for Autism Spectrum Disorder”, Accepted for publication in Neurology India
  • Indiradevi KP, Suhara EM, Poovathinal SA, Anitha A (2022) Distinguishing cognitive states using electroencephalography local activation and functional connectivity patterns. Biomed Signal Process Control. 77: 103742
  • James J, Iype M, Surendran MO, Anitha A, Thomas SV. The genetic landscape of polymicrogyria. Ann Ind Acad Neurol. DOI: 10.4103/aian.aian_97_22.
  • Iype M, Mithran OS, Anitha A , Iype M. Congenital muscular dystrophy due to POMGNT1 mutation presenting as cardioembolic stroke - A case report. Ann Ind Acad Neurol. DOI: 10.4103/aian. aian_944_21.
  • Suhail TA, Indiradevi KP, Suhara EM, Poovathinal SA, Anitha A. Effect of smartphone distractions on cognitive performance in adolescents: An Electroencephalography Approach. Basic ClinNeurosci. DOI: 10.32598/bcn.2021.2295.2
  • Anitha A, Poovathinal SA, Viswambharan V, Thanseem I, Iype M, Anoop U, Sumitha PS, Parakkal R, Vasu MM (2022) MECP2 mutations in the Rett syndrome patients from south India Neurol India. 70: 249-253.
  • Suhail TA, Indiradevi KP, Suhara EM, Poovathinal SA, Anitha A (2021) Electroencephalography-based detection of cognitive state during learning tasks: An extensive approach. Cogn Brain BehavInterdiscip J. XXV:157-178
  • Anitha A, Viswambharan V, Thanseem I, Parakkal R, Sumitha PS, Vasu MM (2021) Vitamins and cognition: A nutrigenomics perspective. CurrNutr Food Sci. 17:348-362
  • Lohithakshan, N. M (2021). An Overview on Learning Disability. In Ayurveda Physician MasikaGoldern Jubilee Special Edition 2021
  • Varghese M, Rani S, Nair AK. The role of working memory as a significant determinant of academic performance. Santosh Univ J Health Sci 2021;7:34-7
  • Spino Cerebellar Degeneration with interesting features. Nair K.G, Suresh.P.A. JAPI, 1986 Nov.
  • Speech and Language Assessment Battery (SLAB) in Indian languages. Suresh.P.A, Maya.S.,Mohan.P.K. ISDL publications Thiruvananthapuram 1993.
  • Case studies on Aphasia - Derivations of Brain mechanisms of language processing from observations of subject with communicative disorders. “Brain and Language”. Suresh.P.A, Maya.S, Mohan.P.K. Seminar Proceedings, ISDL Publications, Thiruvananthapuram. PP 153 - 190, 1994,
  • Rehabilitation of Communicative Disorders: Experience outcome and newer perspectives “Brain and Language”,Maya.S, Suresh.P.A. Seminar Proceedings, 210; 1994, ISDL Publications, Thiruvananthapuram.
  • Brain and Language Seminar Suresh.P.A, Annie Monsy, Maya.S. (Edts) Proceedings, ISDL.
  • Landau – Kleffner Syndrome: Clinical Electro encephalographical, neuro radiological and speech pathology characteristics, Suresh. P.A, Maya.S, Praleema. L, Varghese. N, Santhosh Kumar, Radhakrishnan. K –Proceedings of Fourth Annual Conference of Indian Academy of Neurology- September 27-29, 1996 – Page -31
  • A new coding system for English alphabets with potential applications in the language rehabilitation of mentally retarded, linguistically handicapped and in computer science. P.A.Suresh, S.Maya, Koruth P. Varghese. IJD, VolXXIV No.1
  • Acute Pseudobulbar Mutism: A patient with an unusual stroke syndrome associated with good functional recovery. B.Santoshkumar, P.Abdu Rahiman, P.A Suresh, K Radhakrishnan. JAPI 1996, Vol.44, No.8, 567-568.
  • Motor Neuron Syndrome and Thymoma, Pandian JD, Mathuranath PS, Suresh PA, Radhakrishnan K. Myasthenia Gravis, Neurology India 46, 232-234, 1998.
  • Subclinical hyperthyroidism and hyperkinetic behaviour in children. Suresh PA, Sebastian S, George A, Radhakrishnan K. Pediatr Neurol 1999; 20: 192-194
  • Developmental Gerstmann’s Syndrome - A distinct clinical entity of learning disabilities. Suresh PA, Sebastian S. Pediatr Neurol 2000; 22: 000-000
  • Epidemiological and neurological aspects of learning disabilities. Suresh PA, Swapna Sebastian. Learning Disabilities in India-Willing the mind to learn, edited by Prathibha Karanth and Joe Rozario, SAGE Publications 2003-30-43
  • Congenital Suprabulbarpalsy -a distinctive clinical entity with heterogeneity causes. Suresh PA, Deepa C. Developmental Medicine and Clinical Neurology 2004,46:617-625
  • Autism Early Detection and Management. P.A.Suresh, Dept. of Publication, Aryavaidyasala, Kottakkal, Kerala 2010, Kottakkal Series 96: page 19-101

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