Search Results - Raga, Sharika

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  1. 1
    Developmental and epileptic encephalopathies: recognition and approaches to care

    Developmental and epileptic encephalopathies: recognition and approaches to care by Raga, Sharika, Specchio, Nicola, Rheims, Sylvain, Wilmshurst, Jo M.

    Published in Epileptic disorders
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  2. 2
    Normal Outcome With Prenatal Intervention for Riboflavin Transporter Defect

    Normal Outcome With Prenatal Intervention for Riboflavin Transporter Defect by Elks, Natasha, Wilmshurst, Jo M., Raga, Sharika V.

    Published in Pediatric neurology
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  3. 3
    Epileptic spasms: A South African overview of aetiologies, interventions, and outcomes

    Epileptic spasms: A South African overview of aetiologies, interventions, and outcomes by Raga, Sharika V., Essajee, Farida, Solomons, Regan, Van Toorn, Ronald, Wilmshurst, Jo M.

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  4. 4
    Electroclinical markers to differentiate between focal and generalized epilepsies

    Electroclinical markers to differentiate between focal and generalized epilepsies by Raga, Sharika, Rheims, Sylvain, Specchio, Nicola, Wilmshurst, Jo M.

    Published in Epileptic disorders
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  5. 5
    Epileptic spasms: Evidence for oral corticosteroids and implications for low and middle income countries

    Epileptic spasms: Evidence for oral corticosteroids and implications for low and middle income countries by Raga, Sharika V., Wilmshurst, Jo M.

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  6. 6
    A case for genomic medicine in South African paediatric patients with neuromuscular disease

    A case for genomic medicine in South African paediatric patients with neuromuscular disease by Raga, Sharika V, Wilmshurst, Jo Madeleine, Smuts, Izelle, Meldau, Surita, Bardien, Soraya, Schoonen, Maryke, van der Westhuizen, Francois Hendrikus

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  7. 7
    The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegia

    The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegia by Mahungu, Amokelani C., Steyn, Elizabeth, Floudiotis, Niki, Wilson, Lindsay A., Vandrovcova, Jana, Reilly, Mary M., Record, Christopher J., Benatar, Michael, Wu, Gang, Raga, Sharika, Wilmshurst, Jo M., Naidu, Kireshnee, Hanna, Michael, Nel, Melissa, Heckmann, Jeannine M.

    Published in Frontiers in neurology
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  8. 8
    A novel mitochondrial DNA variant in MT-ND6: m.14430A>C p.(Trp82Gly) identified in a patient with Leigh syndrome and complex I deficiency

    A novel mitochondrial DNA variant in MT-ND6: m.14430A>C p.(Trp82Gly) identified in a patient with Leigh syndrome and complex I deficiency by Meldau, Surita, Ackermann, Sally, Riordan, Gillian, van der Watt, George F., Spencer, Careni, Raga, Sharika, Khan, Kashief, Blackhurst, Dee M., van der Westhuizen, Francois H.

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  9. 9
    Paediatric neuromuscular diseases in Africa: access to care

    Paediatric neuromuscular diseases in Africa: access to care by Raga, Sharika, Baranello, Giovanni, Jungbluth, Heinz, Wilmshurst, Jo M.

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