Fasaludeen A - Search Results

1

Spectrum of Leukodystrophy and Genetic Leukoencephalopathy in Indian Population Diagnosed by Clinical Exome Sequencing and Clinical Utility.

Manisha KY, Fasaludeen A, Poulose P, Menon R, Thomas B, Nair SS, Cherian A, Divya KP, Sundaram S. Manisha KY, et al. Among authors: fasaludeen a. Neurol Genet. 2024 Aug 22;10(5):e200190. doi: 10.1212/NXG.0000000000200190. eCollection 2024 Oct. Neurol Genet. 2024. PMID: 39184309 Free PMC article.

2

Genetic variant interpretation for the neurologist - A pragmatic approach in the next-generation sequencing era in childhood epilepsy.

Fasaludeen A, McTague A, Jose M, Banerjee M, Sundaram S, Madhusoodanan UK, Radhakrishnan A, Menon RN. Fasaludeen A, et al. Epilepsy Res. 2024 Mar;201:107341. doi: 10.1016/j.eplepsyres.2024.107341. Epub 2024 Mar 2. Epilepsy Res. 2024. PMID: 38447235 Review.

3

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: fasaludeen a. 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.

4

Impact of variant subtype on electro-clinical phenotype of Dravet syndrome- a South Indian cohort study.

Krishna S, Fasaludeen A, Jose M, Banerjee M, Sundaram S, Radhakrishnan A, Menon RN. Krishna S, et al. Among authors: fasaludeen a. Seizure. 2024 Feb;115:81-86. doi: 10.1016/j.seizure.2024.01.004. Epub 2024 Jan 14. Seizure. 2024. PMID: 38232648

5

Refinement of the motorised laminectomy-assisted rat spinal cord injury model by analgesic treatment.

Vijayakumar Sreelatha H, Palekkodan H, Fasaludeen A, K Krishnan L, Abelson KSP. Vijayakumar Sreelatha H, et al. Among authors: fasaludeen a. PLoS One. 2024 Jan 16;19(1):e0294720. doi: 10.1371/journal.pone.0294720. eCollection 2024. PLoS One. 2024. PMID: 38227583 Free PMC article.

6

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: fasaludeen a. Seizure. 2024 Feb;115:20-27. doi: 10.1016/j.seizure.2023.12.017. Epub 2024 Jan 3. Seizure. 2024. PMID: 38183824

7

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: fasaludeen a. Indian J Pediatr. 2023 Nov 9. doi: 10.1007/s12098-023-04916-y. Online ahead of print. Indian J Pediatr. 2023. PMID: 37943464

8

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. Among authors: fasaludeen a. 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.

9

Arginase deficiency-An unheralded cause of developmental epileptic encephalopathy.

Pavuluri H, Jose M, Fasaludeen A, Sundaram S, Radhakrishnan A, Banerjee M, Menon RN. Pavuluri H, et al. Among authors: fasaludeen a. Epileptic Disord. 2023 Aug;25(4):556-561. doi: 10.1002/epd2.20081. Epub 2023 May 31. Epileptic Disord. 2023. PMID: 37243436

10

Outcomes of organ preservation treatment in advanced laryngeal carcinoma: A retrospective analysis from a single institution.

Fasaludeen A, Kumar RR, Rafi M, Nazeer F, Prakasan AM, Kumar N, George P, Ramadas K, Thommachan KC. Fasaludeen A, et al. Mol Clin Oncol. 2022 Nov 15;18(1):1. doi: 10.3892/mco.2022.2597. eCollection 2023 Jan. Mol Clin Oncol. 2022. PMID: 36545209 Free PMC article.

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