Jose M - Search Results

1

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: jose j. 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.

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. 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

Women with drug-resistant epilepsy: Surgery or pregnancy first?

Kandraju SS, Jose M, Salini RA, Pavithran V, Samuel Peedicail J, Menon RN, Radhakrishnan A, Cherian A, Abraham M, Vilanilam GC, Thomas SV. Kandraju SS, et al. Among authors: jose m. Epilepsia. 2020 Aug;61(8):1758-1763. doi: 10.1111/epi.16613. Epub 2020 Jul 24. Epilepsia. 2020. PMID: 32706922

4

Malformation risk of new anti-epileptic drugs in women with epilepsy; observational data from the Kerala registry of epilepsy and pregnancy (KREP).

Thomas SV, Jeemon P, Pillai R, Jose M, Lalithakumari AM, Murali S, Sanalkumar A, Salini RA, Pavithran V. Thomas SV, et al. Among authors: jose m. Seizure. 2021 Dec;93:127-132. doi: 10.1016/j.seizure.2021.10.015. Epub 2021 Oct 23. Seizure. 2021. PMID: 34740142 Free article.

5

Utility of clinical exome sequencing in progressive myoclonus epilepsy syndromes: An exploratory analysis.

Jose M, Poulose P, Sundaram S, Radhakrishnan A, Nampoothiri S, Menon RN. Jose M, et al. Clin Genet. 2022 Feb;101(2):270-271. doi: 10.1111/cge.14090. Epub 2021 Dec 9. Clin Genet. 2022. PMID: 34888859 No abstract available.

6

Language, intelligence, and educational outcomes of adolescents with antenatal exposure to antiseizure medications: Prospective data from the Kerala Registry of epilepsy and pregnancy.

Thomas SV, Salim S, Jacob NS, Jose M, Salini RA, Selvaraj S, Gomez TS, Sreedharan H, Jeemon P. Thomas SV, et al. Among authors: jose m. Seizure. 2022 Aug;100:76-81. doi: 10.1016/j.seizure.2022.06.005. Epub 2022 Jun 17. Seizure. 2022. PMID: 35780605 Free article.

7

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: jose m. J Genet. 2022;101:30. J Genet. 2022. PMID: 35791610 Free article.

8

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

9

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: jose 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.

10

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

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