Hasil Pencarian - S Mathuranath Pavagada

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  1. 1
    Neuro-Bechet’s disease: a case series from India

    Neuro-Bechet’s disease: a case series from India oleh Rohan R. Mahale, Sneha Kamath, C. M. Ravindranadh, Hansashree Padmanabha, Pooja Mailankody, Mathuranath Pavagada

    Diterbitkan 2022-12-01
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  2. 2
    ADCY5-related dyskinesia: A genetic cause of early-onset chorea-report of two cases and a novel mutation

    ADCY5-related dyskinesia: A genetic cause of early-onset chorea-report of two cases and a novel mutation oleh Hansashree Padmanabha, Somdattaa Ray, Rohan Mahale, Gautham Arunachal, Pratibha Singhi, Pooja Mailankody, Mathuranath Pavagada

    Diterbitkan 2021-01-01
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  3. 3
    Autosomal dominant cerebral small vessel disease in HTRA1 gene mutation

    Autosomal dominant cerebral small vessel disease in HTRA1 gene mutation oleh Rohan R Mahale, Aakash Agarwal, Jyothi Gautam, Nibu Varghese, Jennifer Kovoor, Pooja Mailankody, Hansashree Padmanabha, Mathuranath Pavagada

    Diterbitkan 2021-01-01
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  4. 4
    A rare treatable cause for atypical frontotemporal dementia with multiple fractures in a young female

    A rare treatable cause for atypical frontotemporal dementia with multiple fractures in a young female oleh Sadanandavalli Retnaswami Chandra, Neeraja Koti, Ganaraja Valakunja Harikrishna, Pooja Mailankody, C Nitin Ramanujam, S Mathuranath Pavagada, Thomas Gregor Issac

    Diterbitkan 2018-01-01
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