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  • Magnetoencephalography imag... Magnetoencephalography imaging of high frequency oscillations strengthens presurgical localization and outcome prediction
    Velmurugan, Jayabal; Nagarajan, Srikantan S; Mariyappa, Narayanan ... Brain, 11/2019, Volume: 142, Issue: 11
    Journal Article
    Peer reviewed
    Open access

    In patients with medically refractory epilepsy, resective surgery is the mainstay of therapy to achieve seizure freedom. However, ∼20-50% of cases have intractable seizures post-surgery due to the ...
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2.
  • Scalp high frequency oscill... Scalp high frequency oscillations (HFOs) in absence epilepsy: An independent component analysis (ICA) based approach
    Chaitanya, Ganne; Sinha, Sanjib; Narayanan, Mariyappa ... Epilepsy research, 09/2015, Volume: 115
    Journal Article
    Peer reviewed

    Highlights • EEG of 9 patients with absence epilepsy were evaluated for occurrence of HFO. • HFOs were associated with inter-ictal generalized (241/454). • HFOs were associated with ictal generalized ...
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  • Functional network connecti... Functional network connectivity imprint in febrile seizures
    Acharya, Ullas V; Kulanthaivelu, Karthik; Panda, Rajanikant ... Scientific reports, 02/2022, Volume: 12, Issue: 1
    Journal Article, Web Resource
    Peer reviewed
    Open access

    Complex febrile seizures (CFS), a subset of paediatric febrile seizures (FS), have been studied for their prognosis, epileptogenic potential and neurocognitive outcome. We evaluated their functional ...
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  • Lost Self to Present Self: ... Lost Self to Present Self: A Case Report of Narrative Therapy for a Woman with Acquired Brain Injury
    Mahajan, Mrinalini; Hegde, Shantala; Sinha, Sanjib Consortium psychiatricum (English ed. Online), 2024, Volume: 5, Issue: 1
    Journal Article
    Peer reviewed
    Open access

    BACKGROUND: Psychotherapy for people with acquired brain injury (ABI) is considered to be an important component of a holistic neuropsychological rehabilitation approach. This helps in making sense ...
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  • Enhancing Precision in Medi... Enhancing Precision in Medical Imaging: A 3D CNN Approach for Fiducial Point Detection in MRI Data
    Suhas, M. V.; Sinha, Sanjib; Mariyappa, N. ... IEEE access, 2024, Volume: 12
    Journal Article
    Peer reviewed
    Open access

    The significance of fiducial marker detection in neuroimaging cannot be overstated, as these markers serve as vital reference points for accurate spatial alignment during image registration. Our ...
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  • PMP22 Gene–Associated Neuro... PMP22 Gene–Associated Neuropathies: Phenotypic Spectrum in a Cohort from India
    Nagappa, Madhu; Sharma, Shivani; Govindaraj, Periyasamy ... Journal of molecular neuroscience, 05/2020, Volume: 70, Issue: 5
    Journal Article
    Peer reviewed

    Reports of spectrum of clinical manifestations in PMP22 gene–associated neuropathies (duplication/mutations) are scarce. To identify the frequency of PMP22 gene variations and establish their ...
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  • Contribution of nuclear and... Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome
    Chakrabarty, Sanjiban; Govindaraj, Periyasamy; Sankaran, Bindu Parayil ... Journal of neurology, 06/2021, Volume: 268, Issue: 6
    Journal Article
    Peer reviewed
    Open access

    Background Mitochondrial disorders are clinically complex and have highly variable phenotypes among all inherited disorders. Mutations in mitochon drial DNA (mtDNA) and nuclear genome or both have ...
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  • Epilepsy: Indian perspective Epilepsy: Indian perspective
    Santhosh, Nandanavana Subbareddy; Sinha, Sanjib; Satishchandra, Parthasarathy Annals of Indian Academy of Neurology, 03/2014, Volume: 17, Issue: Suppl 1
    Journal Article
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    Open access

    There are 50 million people living with epilepsy worldwide, and most of them reside in developing countries. About 10 million persons with epilepsy are there in India. Many people with active ...
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  • Clinico-pathological and Mo... Clinico-pathological and Molecular Spectrum of Mitochondrial Polymerase γ Mutations in a Cohort from India
    Deepha, Sekar; Govindaraj, Periyasamy; Sankaran, Bindu Parayil ... Journal of molecular neuroscience, 11/2021, Volume: 71, Issue: 11
    Journal Article
    Peer reviewed

    Polymerase γ catalytic subunit ( POLG ), a nuclear gene, encodes the enzyme responsible for mitochondrial DNA (mtDNA) replication. POLG mutations are a major cause of inherited mitochondrial ...
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  • Genetic analysis of ATP7B i... Genetic analysis of ATP7B in 102 south Indian families with Wilson disease
    Singh, Nivedita; Kallollimath, Pradeep; Shah, Mohd Hussain ... PloS one, 05/2019, Volume: 14, Issue: 5
    Journal Article
    Peer reviewed
    Open access

    Wilson disease (WD) is an autosomal recessive disorder, characterized by excessive deposition of copper in various parts of the body, mainly in the liver and brain. It is caused by mutations in ...
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