Rudrabhatla PK - Search Results

1

Generalized Stiffness in Hereditary Hyperekplexia Responsive to Trihexyphenidyl: A Novel Finding.

Rudrabhatla PK, Divya KP, Fasaludeen A, Menon RN, Cherian A, Urulangodi M, Sundaram S. Rudrabhatla PK, et al. Clin Pediatr (Phila). 2024 Jul;63(7):885-888. doi: 10.1177/00099228231203300. Epub 2023 Oct 29. Clin Pediatr (Phila). 2024. PMID: 37899614 No abstract available.

2

Unmasking the entity of 'drug-resistant' perioral myoclonia with absences: the twitches, darts and domes!

Rudrabhatla PK, Er S, Radhakrishnan A, Menon RN. Rudrabhatla PK, et al. Epileptic Disord. 2021 Apr 1;23(2):313-324. doi: 10.1684/epd.2021.1265. Epileptic Disord. 2021. PMID: 33851919

3

How does "locus of control" affect persons with epilepsy?

Boddu VK, Rebello A, Chandrasekharan SV, Rudrabhatla PK, Chandran A, Ravi S, Unnithan G, Menon RN, Cherian A, Radhakrishnan A. Boddu VK, et al. Among authors: rudrabhatla pk. Epilepsy Behav. 2021 Oct;123:108257. doi: 10.1016/j.yebeh.2021.108257. Epub 2021 Aug 20. Epilepsy Behav. 2021. PMID: 34425327

4

Visual-sensitive epilepsy in GLUT-1 deficiency syndrome: Expanding the phenotype.

Fazal A, Jose M, Rudrabhatla PK, Chandrasekharan SV, Sundaram S, Radhakrishnan A, Banerjee M, Menon RN. Fazal A, et al. Among authors: rudrabhatla pk. Epileptic Disord. 2023 Apr;25(2):265-268. doi: 10.1002/epd2.20008. Epub 2023 May 4. Epileptic Disord. 2023. PMID: 37358920 No abstract available.

5

Metabolic causes of pediatric developmental & epileptic encephalopathies (DEE)- genetic variant analysis in a south Indian cohort.

Jose M, Fasaludeen A, Pavuluri H, Rudrabhatla PK, Chandrasekharan SV, Jose J, Banerjee M, Sundaram S, Radhakrishnan A, Menon RN. Jose M, et al. Among authors: rudrabhatla pk. Seizure. 2024 Feb;115:20-27. doi: 10.1016/j.seizure.2023.12.017. Epub 2024 Jan 3. Seizure. 2024. PMID: 38183824

6

Challenges in genetic testing for metabolic causes of developmental epileptic encephalopathy- relevance of genotype-phenotype correlations.

Jose M, Fasaludeen A, Pavuluri H, Rudrabhatla PK, Chandrasekharan SV, Jose J, Banerjee M, Sundaram S, Radhakrishnan A, Menon RN. Jose M, et al. Among authors: rudrabhatla pk. Seizure. 2024 Apr;117:307-308. doi: 10.1016/j.seizure.2024.02.012. Epub 2024 Feb 20. Seizure. 2024. PMID: 38402011 No abstract available.

7

Teaching NeuroImages: Ohtahara Syndrome due to Unilateral Perisylvian Polymicrogyria.

Sekar S, Rudrabhatla P, Selvadasan V, Thomas B, Kesavadas C. Sekar S, et al. Neurology. 2021 May 11;96(19):e2456-e2457. doi: 10.1212/WNL.0000000000011497. Epub 2021 Jan 5. Neurology. 2021. PMID: 33402442 No abstract available.

8

Superficial Siderosis Due to Spinal Myxopapillary Ependymoma Mimicking Idiopathic Intracranial Hypertension.

Rudrabhatla P, Sabarish S, Nair SS, George T, Divakar G, Sylaja PN. Rudrabhatla P, et al. Ann Indian Acad Neurol. 2022 Jan-Feb;25(1):156-157. doi: 10.4103/aian.AIAN_186_21. Epub 2021 Oct 11. Ann Indian Acad Neurol. 2022. PMID: 35342259 Free PMC article. No abstract available.

9

Isolated Myelitis and Intramedullary Spinal Cord Abscess in Melioidosis-A Case Report.

Rudrabhatla P, Nair SS, George J, Sekar S, Ponnambath DK. Rudrabhatla P, et al. Neurohospitalist. 2022 Jan;12(1):131-136. doi: 10.1177/19418744211025386. Epub 2021 Jun 16. Neurohospitalist. 2022. PMID: 34950401 Free PMC article.

10

Teaching NeuroImages: Rare Adult-Onset Genetic Leukoencephalopathy.

Rudrabhatla P, Sabarish S, Ramachandran H, Nair SS. Rudrabhatla P, et al. Neurology. 2021 May 18;96(20):e2561-e2562. doi: 10.1212/WNL.0000000000011233. Epub 2020 Nov 18. Neurology. 2021. PMID: 33208544 No abstract available.

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