Hasil Pencarian - Annapurna Poduri

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  1. 1
    KCNQ2‐DEE: developmental or epileptic encephalopathy?

    KCNQ2‐DEE: developmental or epileptic encephalopathy? oleh Anne T. Berg, Sonal Mahida, Annapurna Poduri

    Diterbitkan 2021-03-01
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  2. 2
    Brain somatic mosaicism in epilepsy: Bringing results back to the clinic

    Brain somatic mosaicism in epilepsy: Bringing results back to the clinic oleh Alissa M. D'Gama, Annapurna Poduri

    Diterbitkan 2023-06-01
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  3. 3
    Compound heterozygosity with PRRT2: Pushing the phenotypic envelope in genetic epilepsies

    Compound heterozygosity with PRRT2: Pushing the phenotypic envelope in genetic epilepsies oleh Christelle Moufawad El Achkar, Beth Rosen Sheidley, Declan O'Rourke, Masanori Takeoka, Annapurna Poduri

    Diterbitkan 2019-01-01
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  4. 4
    Clinical Application of Epilepsy Genetics in Africa: Is Now the Time?

    Clinical Application of Epilepsy Genetics in Africa: Is Now the Time? oleh Alina I. Esterhuizen, Alina I. Esterhuizen, Gemma L. Carvill, Rajkumar S. Ramesar, Rajkumar S. Ramesar, Symon M. Kariuki, Charles R. Newton, Charles R. Newton, Annapurna Poduri, Annapurna Poduri, Jo M. Wilmshurst, Jo M. Wilmshurst

    Diterbitkan 2018-05-01
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  5. 5
    Global neurology: It's time to take notice

    Global neurology: It's time to take notice oleh Seward B. Rutkove, Annapurna Poduri, Robert G. Holloway, Scott L. Pomeroy, Justin C. McArthur

    Diterbitkan 2023-05-01
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  6. 6
    Microarray Noninvasive Neuronal Seizure Recordings from Intact Larval Zebrafish.

    Microarray Noninvasive Neuronal Seizure Recordings from Intact Larval Zebrafish. oleh Michaela Meyer, Sameer C Dhamne, Christopher M LaCoursiere, Dimira Tambunan, Annapurna Poduri, Alexander Rotenberg

    Diterbitkan 2016-01-01
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  7. 7
    Correction: Microarray Noninvasive Neuronal Seizure Recordings from Intact Larval Zebrafish.

    Correction: Microarray Noninvasive Neuronal Seizure Recordings from Intact Larval Zebrafish. oleh Michaela Meyer, Sameer C Dhamne, Christopher M LaCoursiere, Dimira Tambunan, Annapurna Poduri, Alexander Rotenberg

    Diterbitkan 2016-01-01
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  8. 8
    Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain

    Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain oleh Xuyu Cai, Gilad D. Evrony, Hillel S. Lehmann, Princess C. Elhosary, Bhaven K. Mehta, Annapurna Poduri, Christopher A. Walsh

    Diterbitkan 2015-02-01
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  9. 9
    EEG band power and phase‐amplitude coupling in patients with Dravet syndrome

    EEG band power and phase‐amplitude coupling in patients with Dravet syndrome oleh Joanne C. Hall, Shahid Bashir, Melissa Tsuboyama, Raidah Al‐Bradie, Ali Mir, Mona Ali, Annapurna Poduri, Alexander Rotenberg

    Diterbitkan 2024-06-01
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  10. 10
    Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain

    Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain oleh Xuyu Cai, Gilad D. Evrony, Hillel S. Lehmann, Princess C. Elhosary, Bhaven K. Mehta, Annapurna Poduri, Christopher A. Walsh

    Diterbitkan 2014-09-01
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  11. 11
    Trends in resource utilization by children with neurological impairment in the United States inpatient health care system: a repeat cross-sectional study.

    Trends in resource utilization by children with neurological impairment in the United States inpatient health care system: a repeat cross-sectional study. oleh Jay G Berry, Annapurna Poduri, Joshua L Bonkowsky, Jing Zhou, Dionne A Graham, Chelsea Welch, Heather Putney, Rajendu Srivastava

    Diterbitkan 2012-01-01
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  12. 12
    Mosaic and non-mosaic protocadherin 19 mutation leads to neuronal hyperexcitability in zebrafish

    Mosaic and non-mosaic protocadherin 19 mutation leads to neuronal hyperexcitability in zebrafish oleh Barbara K. Robens, Xinzhu Yang, Christopher M. McGraw, Laura H. Turner, Carsten Robens, Summer Thyme, Alexander Rotenberg, Annapurna Poduri

    Diterbitkan 2022-07-01
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  13. 13
    Clinical utility of a genetic diagnosis in individuals with cerebral palsy and related motor disorders

    Clinical utility of a genetic diagnosis in individuals with cerebral palsy and related motor disorders oleh Alexandra Santana Almansa, Dustin L. Gable, Zoë Frazier, Abigail Sveden, Aisling Quinlan, Maya Chopra, Sara A. Lewis, Michael Kruer, Annapurna Poduri, Siddharth Srivastava

    Diterbitkan 2024-02-01
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  14. 14
    A mouse model of DEPDC5-related epilepsy: Neuronal loss of Depdc5 causes dysplastic and ectopic neurons, increased mTOR signaling, and seizure susceptibility

    A mouse model of DEPDC5-related epilepsy: Neuronal loss of Depdc5 causes dysplastic and ectopic neurons, increased mTOR signaling, and seizure susceptibility oleh Christopher J. Yuskaitis, Brandon M. Jones, Rachel L. Wolfson, Chloe E. Super, Sameer C. Dhamne, Alexander Rotenberg, David M. Sabatini, Mustafa Sahin, Annapurna Poduri

    Diterbitkan 2018-03-01
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  15. 15
    Posterior-onset Rasmussen's encephalitis with ipsilateral cerebellar atrophy and uveitis resistant to rituximab

    Posterior-onset Rasmussen's encephalitis with ipsilateral cerebellar atrophy and uveitis resistant to rituximab oleh Arnold J. Sansevere, Lauren A. Henderson, Coral M. Stredny, Sanjay P. Prabhu, Ankoor Shah, Robert Sundel, Joseph Madsen, Chantal Dufreney, Annapurna Poduri, Mark P. Gorman

    Diterbitkan 2020-01-01
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  16. 16
    High-throughput brain activity mapping and machine learning as a foundation for systems neuropharmacology

    High-throughput brain activity mapping and machine learning as a foundation for systems neuropharmacology oleh Xudong Lin, Xin Duan, Claire Jacobs, Jeremy Ullmann, Chung-Yuen Chan, Siya Chen, Shuk-Han Cheng, Wen-Ning Zhao, Annapurna Poduri, Xin Wang, Stephen J. Haggarty, Peng Shi

    Diterbitkan 2018-12-01
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  17. 17
    Uridine‐responsive epileptic encephalopathy due to inherited variants in CAD: A Tale of Two Siblings

    Uridine‐responsive epileptic encephalopathy due to inherited variants in CAD: A Tale of Two Siblings oleh Christopher M. McGraw, Sonal Mahida, Parul Jayakar, Hyun Yong Koh, Alan Taylor, Trevor Resnick, Lance Rodan, Marc A. Schwartz, Ayesha Ejaz, Vijay G. Sankaran, Gerard Berry, Annapurna Poduri

    Diterbitkan 2021-03-01
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  18. 18
    P208: Insights into diagnostic yield and novel genetic etiologies for unilateral polymicrogyria

    P208: Insights into diagnostic yield and novel genetic etiologies for unilateral polymicrogyria oleh Abbe Lai, Jennifer Neil, Lance Rodan, Achkar Moufawad El Achkar, Shyam Akula, Anthony Barkovich, Allen Chen, Diane Shao, Kimberly Wiltrout, Ganeshwaran Mochida, Heather Olson, Edward Yang, Annapurna Poduri, Christopher Walsh

    Diterbitkan 2024-01-01
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  19. 19
    Acute multi-sgRNA knockdown of KEOPS complex genes reproduces the microcephaly phenotype of the stable knockout zebrafish model.

    Acute multi-sgRNA knockdown of KEOPS complex genes reproduces the microcephaly phenotype of the stable knockout zebrafish model. oleh Tilman Jobst-Schwan, Johanna Magdalena Schmidt, Ronen Schneider, Charlotte A Hoogstraten, Jeremy F P Ullmann, David Schapiro, Amar J Majmundar, Amy Kolb, Kaitlyn Eddy, Shirlee Shril, Daniela A Braun, Annapurna Poduri, Friedhelm Hildebrandt

    Diterbitkan 2018-01-01
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  20. 20
    A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations.

    A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations. oleh Xiaolin Zhu, Raghavendra Padmanabhan, Brett Copeland, Joshua Bridgers, Zhong Ren, Sitharthan Kamalakaran, Ailbhe O'Driscoll-Collins, Samuel F Berkovic, Ingrid E Scheffer, Annapurna Poduri, Davide Mei, Renzo Guerrini, Daniel H Lowenstein, Andrew S Allen, Erin L Heinzen, David B Goldstein

    Diterbitkan 2017-11-01
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