Banerjee M - Search Results

1

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: banerjee m. Epileptic Disord. 2023 Aug;25(4):556-561. doi: 10.1002/epd2.20081. Epub 2023 May 31. Epileptic Disord. 2023. PMID: 37243436

2

Pharmacogenetic evaluation of ABCB1, Cyp2C9, Cyp2C19 and methylene tetrahydrofolate reductase polymorphisms in teratogenicity of anti-epileptic drugs in women with epilepsy.

Jose M, Banerjee M, Mathew A, Bharadwaj T, Vijayan N, Thomas SV. Jose M, et al. Among authors: banerjee m. Ann Indian Acad Neurol. 2014 Jul;17(3):259-66. doi: 10.4103/0972-2327.138475. Ann Indian Acad Neurol. 2014. PMID: 25221392 Free PMC article.

3

C12orf57 pathogenic variants: a unique cause of developmental encephalopathy in a south Indian child.

Alfiya F, Jose M, Chandrasekharan SV, Sundaram S, Urulangodi M, Thomas B, Radhakrishnan A, Banerjee M, Menon RN. Alfiya F, et al. Among authors: banerjee m. J Genet. 2022;101:30. J Genet. 2022. PMID: 35791610 Free article.

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

6

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: banerjee m. Seizure. 2024 Feb;115:81-86. doi: 10.1016/j.seizure.2024.01.004. Epub 2024 Jan 14. Seizure. 2024. PMID: 38232648

7

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: banerjee m. 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.

8

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. Among authors: banerjee m. Epilepsy Res. 2024 Mar;201:107341. doi: 10.1016/j.eplepsyres.2024.107341. Epub 2024 Mar 2. Epilepsy Res. 2024. PMID: 38447235 Review.

9

Failure to find association between febrile seizures and SCN1A rs3812718 polymorphism in south Indian patients with mesial temporal lobe epilepsy and hippocampal sclerosis.

Balan S, Vellichirammal NN, Banerjee M, Radhakrishnan K. Balan S, et al. Among authors: banerjee m. Epilepsy Res. 2012 Sep;101(3):288-92. doi: 10.1016/j.eplepsyres.2012.04.009. Epub 2012 May 10. Epilepsy Res. 2012. PMID: 22578703

10

Genetic association analysis of ATP binding cassette protein family reveals a novel association of ABCB1 genetic variants with epilepsy risk, but not with drug-resistance.

Balan S, Bharathan SP, Vellichiramal NN, Sathyan S, Joseph V, Radhakrishnan K, Banerjee M. Balan S, et al. Among authors: banerjee m. PLoS One. 2014 Feb 21;9(2):e89253. doi: 10.1371/journal.pone.0089253. eCollection 2014. PLoS One. 2014. PMID: 24586633 Free PMC article.

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