Search Results - Chandrasekharan, Soumya V

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  1. 1
    Challenges in genetic testing for metabolic causes of developmental epileptic encephalopathy- relevance of genotype-phenotype correlations

    Challenges in genetic testing for metabolic causes of developmental epileptic encephalopathy- relevance of genotype-phenotype correlations by Jose, Manna, Fasaludeen, Alfiya, Pavuluri, Harini, Rudrabhatla, Pavan Kumar, Chandrasekharan, Soumya V., Jose, Jithu, Banerjee, Moinak, Sundaram, Soumya, Radhakrishnan, Ashalatha, Menon, Ramshekhar N.

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  2. 2
    Effect of seizure viewing on psychological outcome in persons with epilepsy

    Effect of seizure viewing on psychological outcome in persons with epilepsy by Chandrasekharan, Soumya V., Menon, Ramshekhar, Cherian, Ajith, Radhakrishnan, Ashalatha

    Published in Epilepsy & behavior
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  3. 3
    Metabolic causes of pediatric developmental & epileptic encephalopathies (DEE)- genetic variant analysis in a south Indian cohort

    Metabolic causes of pediatric developmental & epileptic encephalopathies (DEE)- genetic variant analysis in a south Indian cohort by Jose, Manna, Fasaludeen, Alfiya, Pavuluri, Harini, Rudrabhatla, Pavan Kumar, Chandrasekharan, Soumya V., Jose, Jithu, Banerjee, Moinak, Sundaram, Soumya, Radhakrishnan, Ashalatha, Menon, Ramshekhar N.

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  4. 4
    Myoneuropathic presentation of limb girdle muscular dystrophy R8 with a novel TRIM32 mutation

    Myoneuropathic presentation of limb girdle muscular dystrophy R8 with a novel TRIM32 mutation by Chandrasekharan, Soumya V., Sundaram, Soumya, Malaichamy, Sivasankar, Poyuran, Rajalakshmy, Nair, Sruthi S.

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  5. 5
    Satisfaction among persons with epilepsy towards physical consultation versus online video consultation for follow-up

    Satisfaction among persons with epilepsy towards physical consultation versus online video consultation for follow-up by Rebello, Alex, Chandrasekharan, Soumya V., Kumar Rudrabhatla, Pavan, Vincent, Sanu J., Menon, Ramshekhar N., Radhakrishnan, Ashalatha

    Published in Epilepsy & behavior
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  6. 6
    Charcot-Marie-Tooth disease type 2S: identical novel missense mutation of IGHMBP2 gene in two unrelated families

    Charcot-Marie-Tooth disease type 2S: identical novel missense mutation of IGHMBP2 gene in two unrelated families by Chandrasekharan, Soumya V., Nair, Sruthi S., Ganapathy, Aparna, Mannan, Ashraf U., Sundaram, Soumya

    Published in Neurological sciences
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  7. 7
    How does “locus of control” affect persons with epilepsy?

    How does “locus of control” affect persons with epilepsy? by Boddu, Vijay Kumar, Rebello, Alex, Chandrasekharan, Soumya V., Rudrabhatla, Pavan Kumar, Chandran, Anuvitha, Ravi, Swathy, Unnithan, Gopeekrishnan, Menon, Ramshekhar N., Cherian, Ajith, Radhakrishnan, Ashalatha

    Published in Epilepsy & behavior
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  8. 8
    Visual‐sensitive epilepsy in GLUT‐1 deficiency syndrome: Expanding the phenotype

    Visual‐sensitive epilepsy in GLUT‐1 deficiency syndrome: Expanding the phenotype by Fazal, Alfiya, Jose, Manna, Rudrabhatla, Pavan Kumar, Chandrasekharan, Soumya V., Sundaram, Soumya, Radhakrishnan, Ashalatha, Banerjee, Moinak, Menon, Ramshekhar N.

    Published in Epileptic disorders
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  9. 9
    C12orf57 pathogenic variants: a unique cause of developmental encephalopathy in a south Indian child

    C12orf57 pathogenic variants: a unique cause of developmental encephalopathy in a south Indian child by Alfiya, F., Jose, Manna, Chandrasekharan, Soumya V., Sundaram, Soumya, Urulangodi, Madhusoodanan, Thomas, Bejoy, Radhakrishnan, Ashalatha, Banerjee, Moinak, Menon, Ramshekhar N.

    Published in Journal of genetics
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  10. 10
    Does Etiology and Hypsarrhythmia Subtype Influence Outcome in West Syndrome? Challenges Encountered from a Referral Center Perspective

    Does Etiology and Hypsarrhythmia Subtype Influence Outcome in West Syndrome? Challenges Encountered from a Referral Center Perspective by Chandrasekharan, Soumya, Menon, Ramshekhar, Nanda, Satyan, Nair, Jeevan, Radhakrishnan, Ashalatha, Cherian, Ajith, Thomas, Sanjeev

    Published in Neurology India
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  11. 11
    Myoneuropathic presentation of limb girdle muscular dystrophy R8 with a novel TRIM32 mutation

    Myoneuropathic presentation of limb girdle muscular dystrophy R8 with a novel TRIM32 mutation by Chandrasekharan, Soumya V, Sundaram, Soumya, Malaichamy, Sivasankar, Poyuran, Rajalakshmy, Nair, Sruthi S

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