Search Results - UK, Kandha Kumar

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  1. 1
    Acute Flaccid Paralysis Due to KCNJ16 Channelopathy

    Acute Flaccid Paralysis Due to KCNJ16 Channelopathy by Joon, Preeti, Gunasekaran, Pradeep Kumar, UK, Kandha Kumar, Singh, Kuldeep, Saini, Lokesh

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  2. 2
    Etanercept: A Potential Option in Refractory Complicated Neurocysticercosis

    Etanercept: A Potential Option in Refractory Complicated Neurocysticercosis by Saini, Lokesh, Gunasekaran, Pradeep Kumar, UK, Kandha Kumar, Gupta, Rahul, Tiwari, Sarbesh

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  3. 3
    Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene

    Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene by Gunasekaran, Pradeep Kumar, Kumar, Ashna, UK, Kandha Kumar, Laxmi, Veena, Tiwari, Sarbesh, Saini, Lokesh

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  4. 4
    Kernicterus caused by a rare genetic variant of Crigler-Najjar Syndrome (c.826G>C)

    Kernicterus caused by a rare genetic variant of Crigler-Najjar Syndrome (c.826G>C) by Agarwal, Saurabh, UK, Kandha Kumar, Parameswaran, Arun Sree, Saini, Lokesh, Singh, Kuldeep

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  5. 5
    Eating Epilepsy in an Acute Lymphocytic Leukemia Survivor

    Eating Epilepsy in an Acute Lymphocytic Leukemia Survivor by Gunasekaran, Pradeep Kumar, UK, Kandha Kumar, Gupta, Rahul, Kumar, Lokesh, Saini, Lokesh

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  6. 6
    Starry sky and leukodystrophy-like pattern in multiple neurocysticercosis

    Starry sky and leukodystrophy-like pattern in multiple neurocysticercosis by Tiwari, Sarbesh, Gunasekaran, Pradeep Kumar, UK, Kandha Kumar, Saini, Lokesh

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  7. 7
    Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene

    Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene by Gunasekaran, Pradeep Kumar, Kumar, Ashna, Uk, Kandha Kumar, Laxmi, Veena, Tiwari, Sarbesh, Saini, Lokesh

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