Search Results - Kumar, Tumulu Seetam

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  1. 1
    Melanin Incontinence, Infantile Stroke, and Negative Genetics in a Case of Incontinentia Pigmenti

    Melanin Incontinence, Infantile Stroke, and Negative Genetics in a Case of Incontinentia Pigmenti by Ananthasubramanian, Sangeeth Thuppanattumadam, Chanrakant, Seemikeri Chinmayi, Kumar, Tumulu Seetam, Rajeswarie, Rangasamy Thiruvengadam, Udupi, Gautham Arunachal, Kenchiah, Raghavendra, Padmanabha, Hansashree

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  2. 2
    Pontine Tegmental Cap Dysplasia: A Rare Brainstem Malformation Mimicking Hereditary Sensory Autonomic Neuropathy

    Pontine Tegmental Cap Dysplasia: A Rare Brainstem Malformation Mimicking Hereditary Sensory Autonomic Neuropathy by Nagaraj, A R, Shravanthi, Guduru, Kumar, Tumulu Seetam, Kenchiah, Raghavendra, Mahale, Rohan, Sandhya, M, Udupi, Gautham Arunachal, Mailankody, Pooja, Mathuranath, P S, Padmanabha, Hansashree

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  3. 3
    Enlightening a ‘Dark Brain’: Essential Insights for Every Stroke Specialist

    Enlightening a ‘Dark Brain’: Essential Insights for Every Stroke Specialist by Samim, M M, Kumar, Tumulu Seetam, Harishma, R S, Kulkarni, Girish Baburao

    Published in Neurology India
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  4. 4
    Genetic spectrum of neuronal ceroid lipofuscinosis & its genotype-phenotype correlation –A single centre experience of 56 cases

    Genetic spectrum of neuronal ceroid lipofuscinosis & its genotype-phenotype correlation –A single centre experience of 56 cases by Thuppanattumadam Ananthasubramanian, Sangeeth, Padmanabha, Hansashree, Ravindranadh, C.M., Kenchiah, Raghavendra, Bhatia, Saloni, Santhoshkumar, Rashmi, Kumar, Tumulu Seetam, Sukrutha, Ramya, Arunachal, Gautham, Karthik, K., Nagappa, Madhu, Nashi, Saraswati, Mahale, Rohan, Viswananthan, L.G., Pooja, M., Nagaraj, A.R., Ravi Shekar, J., Yasha, T.C., Mahadevan, Anita, Sinha, Sanjib

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    Partial loss of desmin expression due to a leaky splice site variant in the human DES gene is associated with neuromuscular transmission defects

    Partial loss of desmin expression due to a leaky splice site variant in the human DES gene is associated with neuromuscular transmission defects by Polavarapu, Kiran, O'Neil, Daniel, Thompson, Rachel, Spendiff, Sally, Nandeesh, Bevinahalli, Vengalil, Seena, Huddar, Akshata, Baskar, Dipti, Arunachal, Gautham, Kotambail, Ananthapadmanabha, Bhatia, Saloni, Tumulu, Seetam Kumar, Matalonga, Leslie, Töpf, Ana, Laurie, Steven, Zeldin, Joshua, Nashi, Saraswati, Unnikrishnan, Gopikrishnan, Nalini, Atchayaram, Lochmüller, Hanns

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  6. 6
    Genetic spectrum of neuronal ceroid lipofuscinosis & its genotype-phenotype correlation -A single centre experience of 56 cases

    Genetic spectrum of neuronal ceroid lipofuscinosis & its genotype-phenotype correlation -A single centre experience of 56 cases by Thuppanattumadam Ananthasubramanian, Sangeeth, Padmanabha, Hansashree, Ravindranadh, C M, Kenchiah, Raghavendra, Bhatia, Saloni, Santhoshkumar, Rashmi, Kumar, Tumulu Seetam, Sukrutha, Ramya, Arunachal, Gautham, Karthik, K, Nagappa, Madhu, Nashi, Saraswati, Mahale, Rohan, Viswananthan, L G, Pooja, M, Nagaraj, A R, Ravi Shekar, J, Yasha, T C, Mahadevan, Anita, Sinha, Sanjib

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