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Page 1
Childhood Neurological Disorders With Hyperhomocystinemia: A Case-Based Review.
Yoganathan S, Bhasin H, Garg D, Malik P, Saini AG, Chandran M, Korula S, Arunachal G, Danda S, Thomas M, Oommen SP, Sharma S. Yoganathan S, et al. Among authors: oommen sp. Pediatr Neurol. 2023 Sep;146:26-30. doi: 10.1016/j.pediatrneurol.2023.06.003. Epub 2023 Jun 13. Pediatr Neurol. 2023. PMID: 37413720
An Indian boy with additional features in Pallister-Killian syndrome.
Shah K, George R, Balla ES, Oommen SP, Padankatti CS, Srivastava VM, Danda S. Shah K, et al. Among authors: oommen sp. Indian J Pediatr. 2012 Sep;79(9):1238-40. doi: 10.1007/s12098-011-0585-8. Epub 2011 Oct 20. Indian J Pediatr. 2012. PMID: 22012142
Cri du chat syndrome: a series of five cases.
Dangare HM, Oommen SP, Sheth AN, Koshy B, Roshan R, Thomas MM, Danda S, Srivastava VM. Dangare HM, et al. Among authors: oommen sp. Indian J Pathol Microbiol. 2012 Oct-Dec;55(4):501-5. doi: 10.4103/0377-4929.107791. Indian J Pathol Microbiol. 2012. PMID: 23455788
Guanidinoacetate Methyltransferase (GAMT) Deficiency, A Cerebral Creatine Deficiency Syndrome: A Rare Treatable Metabolic Disorder.
Yoganathan S, Arunachal G, Kratz L, Varman M, Sudhakar SV, Oommen SP, Jain S, Thomas M, Babuji M. Yoganathan S, et al. Among authors: oommen sp. Ann Indian Acad Neurol. 2020 May-Jun;23(3):419-421. doi: 10.4103/aian.AIAN_172_19. Epub 2020 Jan 3. Ann Indian Acad Neurol. 2020. PMID: 32606564 Free PMC article. No abstract available.
Unusual Presentation of Adrenal Hypoplasia Congenita.
Srinivasaraghavan R, Jagadeesh A, Yoganathan S, Mathai S, Oommen SP. Srinivasaraghavan R, et al. Among authors: oommen sp. Indian J Pediatr. 2020 Oct;87(10):865-866. doi: 10.1007/s12098-020-03239-6. Epub 2020 Jul 9. Indian J Pediatr. 2020. PMID: 32643053 No abstract available.
The Diagnostic Value of Congenital and Nevoid Cutaneous Lesions Associated with Autism Spectrum Disorders in Indian Children- A Case-Control Study.
Varala S, George R, Mathew L, Russell P, Koshy B, Oommen SP, Thomas M, Muthusamy K, Yoganathan S, Jeyaseelan L, Muliyil J. Varala S, et al. Among authors: oommen sp. Indian Dermatol Online J. 2021 Jan 16;12(1):84-89. doi: 10.4103/idoj.IDOJ_275_20. eCollection 2021 Jan-Feb. Indian Dermatol Online J. 2021. PMID: 33768027 Free PMC article.
Metabolic Or Ischemic Stroke in Succinic Semi-Aldehyde Dehydrogenase Deficiency Due to the Homozygous Variant c. 1343 + 1_1343 + 3delGTAinsTT in ALDH5A1.
Yoganathan S, Arunachal G, Kratz L, Varman M, Thomas M, Sudhakar SV, Oommen SP, Danda S. Yoganathan S, et al. Among authors: oommen sp. Ann Indian Acad Neurol. 2021 Mar-Apr;24(2):259-261. doi: 10.4103/aian.AIAN_360_20. Epub 2021 Apr 28. Ann Indian Acad Neurol. 2021. PMID: 34220078 Free PMC article. No abstract available.
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