Sundaram S - Search Results

1

Gyratory Seizures: An Early Clue to Anti-NMDAR Encephalitis.

Vijayaraghavan A, Sundaram S, Sachithanandan S, Sukumaran S. Vijayaraghavan A, et al. Among authors: sundaram s. Indian J Pediatr. 2023 Jun;90(6):622. doi: 10.1007/s12098-023-04566-0. Epub 2023 Apr 1. Indian J Pediatr. 2023. PMID: 37004652 No abstract available.

2

Moyamoya disease: a comparison of long term outcome of conservative and surgical treatment in India.

Sundaram S, Sylaja PN, Menon G, Sudhir J, Jayadevan ER, Sukumaran S, Sreedharan SE, Sarma S. Sundaram S, et al. J Neurol Sci. 2014 Jan 15;336(1-2):99-102. doi: 10.1016/j.jns.2013.10.014. Epub 2013 Oct 16. J Neurol Sci. 2014. PMID: 24183032

3

Pyruvate Dehydrogenase Complex Deficiency Due to PDHA1 Mutation-A Rare Treatable Cause for Episodic Ataxia in Children.

Pavuluri H, F A, Menon RN, Nair SS, Sundaram S. Pavuluri H, et al. Among authors: sundaram s. Indian J Pediatr. 2022 May;89(5):519. doi: 10.1007/s12098-021-04068-x. Epub 2022 Feb 8. Indian J Pediatr. 2022. PMID: 35132535 No abstract available.

4

Teaching NeuroImage: IBA57 Mutation-Associated Infantile Cavitating Leukoencephalopathy.

Cherian A, Yalapalli MK, K P D, Vijayaraghavan A, Sundaram S. Cherian A, et al. Among authors: sundaram s. Neurology. 2022 Jun 14;98(24):1029-1030. doi: 10.1212/WNL.0000000000200671. Epub 2022 Apr 6. Neurology. 2022. PMID: 35387852 No abstract available.

5

Hypomagnesemia-induced encephalopathy with transient torsional nystagmus evolving into downbeat nystagmus: a rare complication of ileostomy.

Paramasivan NK, Yallapalli MK, Sundaram S, Vijayaraghavan A, Sukumaran S. Paramasivan NK, et al. Among authors: sundaram s. Acta Neurol Belg. 2023 Aug;123(4):1545-1547. doi: 10.1007/s13760-022-01997-y. Epub 2022 Jun 22. Acta Neurol Belg. 2023. PMID: 35731376 No abstract available.

6

Autism Spectrum Disorders: Barriers to Implementing Parent-Based Home Programs.

Jose DS, Varma R, Sambasivan SL, Philip L, Sandhya P, Sundaram S. Jose DS, et al. Among authors: sundaram s. Indian J Pediatr. 2023 Jan;90(1):79-82. doi: 10.1007/s12098-022-04383-x. Epub 2022 Nov 18. Indian J Pediatr. 2023. PMID: 36399246

7

Status Epilepticus in Coenzyme A Synthase Protein-Associated Neurodegeneration - Expanding the Clinical Phenotype.

Ajit VK, Selvaraj P, Divya KP, Thomas B, Menon RN, Sundaram S. Ajit VK, et al. Among authors: sundaram s. Indian J Pediatr. 2023 May;90(5):519. doi: 10.1007/s12098-023-04515-x. Epub 2023 Mar 6. Indian J Pediatr. 2023. PMID: 36877387 No abstract available.

8

Movement Disorders in GRIA2-Related Disorder - Expanding the Genetic Spectrum of Developmental Dyskinetic Encephalopathy.

Vijayaraghavan A, Urulangodi M, Ajit Valaparambil K, Sundaram S, Krishnan S. Vijayaraghavan A, et al. Among authors: sundaram s. Mov Disord Clin Pract. 2023 Jun 12;10(8):1222-1224. doi: 10.1002/mdc3.13797. eCollection 2023 Aug. Mov Disord Clin Pract. 2023. PMID: 37635778 Free PMC article. No abstract available.

9

Intrathecal methotrexate induced subacute combined degeneration of spinal cord like presentation in a patient with acute lymphocytic leukaemia.

Krishna S, Vijayaraghavan A, Philip DSJ, Sundaram S, Sukumaran S. Krishna S, et al. Among authors: sundaram s. Acta Neurol Belg. 2024 Apr;124(2):679-681. doi: 10.1007/s13760-023-02418-4. Epub 2023 Oct 30. Acta Neurol Belg. 2024. PMID: 37904078 No abstract available.

10

Clinical Utility of Proband Only Clinical Exome Sequencing in Neurodevelopmental Disorders.

Valaparambil KA, Fasaludeen A, Priya L, Menon RN, Menon R, Sundaram S. Valaparambil KA, et al. Among authors: sundaram s. Indian J Pediatr. 2023 Nov 9. doi: 10.1007/s12098-023-04916-y. Online ahead of print. Indian J Pediatr. 2023. PMID: 37943464

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