Search Results - Selvam, Pavalan Panneer

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  1. 1
    High-grade glioma with pleomorphic and pseudopapillary features (HPAP): a proposed type of circumscribed glioma in adults harboring frequent TP53 mutations and recurrent monosomy 13

    High-grade glioma with pleomorphic and pseudopapillary features (HPAP): a proposed type of circumscribed glioma in adults harboring frequent TP53 mutations and recurrent monosomy 1... by Pratt, Drew, Abdullaev, Zied, Papanicolau-Sengos, Antonios, Ketchum, Courtney, Panneer Selvam, Pavalan, Chung, Hye-Jung, Lee, Ina, Raffeld, Mark, Gilbert, Mark R., Armstrong, Terri S., Pytel, Peter, Borys, Ewa, Klonoski, Joshua M., McCord, Matthew, Horbinski, Craig, Brat, Daniel, Perry, Arie, Solomon, David, Eberhart, Charles, Giannini, Caterina, Quezado, Martha, Aldape, Kenneth

    Published in Acta neuropathologica
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  2. 2
    Molecular and clinicopathologic characteristics of gliomas with EP300::BCOR fusions

    Molecular and clinicopathologic characteristics of gliomas with EP300::BCOR fusions by Wu, Zhichao, Rajan, Sharika, Chung, Hye-Jung, Raffeld, Mark, Panneer Selvam, Pavalan, Schweizer, Leonille, Perry, Arie, Samuel, David, Giannini, Caterina, Ragunathan, Aditya, Frosch, Matthew P., Marshall, Michael S., Boué, Daniel R., Donev, Kliment, Neill, Stewart G., Fernandes, Igor, Resnick, Adam, Rood, Brian, Cummings, Thomas J., Buckley, Anne F., Szymanski, Linda, Neto, Osorio Lopes Abath, Zach, Leor, Colman, Howard, Cheshier, Samuel, Ziskin, Jennifer, Tyagi, Manoj, Capper, David, Abdullaev, Zied, Cimino, Patrick J., Quezado, Martha, Pratt, Drew, Aldape, Kenneth

    Published in Acta neuropathologica
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  3. 3
    P262: First genetically confirmed case of Schinzel-Giedion syndrome from India and literature review of neuroradiological findings

    P262: First genetically confirmed case of Schinzel-Giedion syndrome from India and literature review of neuroradiological findings by Selvam, Pavalan Panneer, G, Paramasivam, Danda, Sumita

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  4. 4
    P321: Expanding the phenotypic spectrum of Currarino syndrome with cardiac anomalies

    P321: Expanding the phenotypic spectrum of Currarino syndrome with cardiac anomalies by Taliercio, Vanina, Akay, Gulsen, Selvam, Pavalan Panneer, Botto, Lorenzo, Underhill, Hunter

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  5. 5
    Recurrent ACVR1 mutations in posterior fossa ependymoma

    Recurrent ACVR1 mutations in posterior fossa ependymoma by Pratt, Drew, Lucas, Calixto-Hope G., Selvam, Pavalan Panneer, Abdullaev, Zied, Ketchum, Courtney, Quezado, Martha, Armstrong, Terri S., Gilbert, Mark R., Papanicolau-Sengos, Antonios, Raffeld, Mark, Choo-Wosoba, Hyoyoung, Chan, Priya, Whipple, Nicholas, Nasrallah, MacLean, Santi, Mariarita, Ramaswamy, Vijay, Giannini, Caterina, Ritzmann, Timothy A., Grundy, Richard G., Burford, Anna, Jones, Chris, Hawkins, Cynthia, Venneti, Sriram, Solomon, David A., Aldape, Kenneth

    Published in Acta neuropathologica
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  6. 6
    Abstract 3428: Development and validation of the plasma monitor test system

    Abstract 3428: Development and validation of the plasma monitor test system by Kelly, Kevin J., Uvalic, Jasmina, Bergeron, Daniel, Burns, Shelbi, Soucy, Melissa, Ananda, Guruprasad, Hesse, Andrew, Selvam, Pavalan Panneer, Reddi, Honey V.

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