Search Results - Fasaludeen, Alfiya

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  1. 1
    Generalized Stiffness in Hereditary Hyperekplexia Responsive to Trihexyphenidyl: A Novel Finding

    Generalized Stiffness in Hereditary Hyperekplexia Responsive to Trihexyphenidyl: A Novel Finding by Rudrabhatla, Pavan Kumar, Divya, K. P., Fasaludeen, Alfiya, Menon, Ramshekhar N., Cherian, Ajith, Urulangodi, Madhusoodanan, Sundaram, Soumya

    Published in Clinical pediatrics
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  2. 2
    Impact of variant subtype on electro-clinical phenotype of Dravet syndrome- a South Indian cohort study

    Impact of variant subtype on electro-clinical phenotype of Dravet syndrome- a South Indian cohort study by Krishna, S, Fasaludeen, Alfiya, Jose, Manna, Banerjee, Moinak, Sundaram, Soumya, Radhakrishnan, Ashalatha, Menon, Ramshekhar N

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  3. 3
    Genetic variant interpretation for the neurologist – A pragmatic approach in the next-generation sequencing era in childhood epilepsy

    Genetic variant interpretation for the neurologist – A pragmatic approach in the next-generation sequencing era in childhood epilepsy by Fasaludeen, Alfiya, McTague, Amy, Jose, Manna, Banerjee, Moinak, Sundaram, Soumya, Madhusoodanan, U.K., Radhakrishnan, Ashalatha, Menon, Ramshekhar N.

    Published in Epilepsy research
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  4. 4
    Arginase deficiency—An unheralded cause of developmental epileptic encephalopathy

    Arginase deficiency—An unheralded cause of developmental epileptic encephalopathy by Pavuluri, Harini, Jose, Manna, Fasaludeen, Alfiya, Sundaram, Soumya, Radhakrishnan, Ashalatha, Banerjee, Moinak, Menon, Ramshekhar N.

    Published in Epileptic disorders
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  5. 5
    Clinical Utility of Proband Only Clinical Exome Sequencing in Neurodevelopmental Disorders

    Clinical Utility of Proband Only Clinical Exome Sequencing in Neurodevelopmental Disorders by Valaparambil, Karthika Ajit, Fasaludeen, Alfiya, Priya, Lakshmi, Menon, Ramshekhar N., Menon, Ramesh, Sundaram, Soumya

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  6. 6
    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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  7. 7
    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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  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
    Spectrum of Leukodystrophy and Genetic Leukoencephalopathy in Indian Population Diagnosed by Clinical Exome Sequencing and Clinical Utility

    Spectrum of Leukodystrophy and Genetic Leukoencephalopathy in Indian Population Diagnosed by Clinical Exome Sequencing and Clinical Utility by Manisha, Karamala Yalapalli, Fasaludeen, Alfiya, Poulose, Prashanth, Menon, Ramshekhar, Thomas, Bejoy, Nair, Sruthi S, Cherian, Ajith, Divya, Kalikavil Puthanveedu, Sundaram, Soumya

    Published in Neurology. Genetics
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