Hasil Pencarian - Kyle Hurth

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  1. 1
    Fatal refractory cardiac arrest as presentation of systemic amyloidosis

    Fatal refractory cardiac arrest as presentation of systemic amyloidosis oleh Peter Chung, Sarah Wheeler, Andrew Fong, Kyle Hurth, Bassam Yaghmour

    Diterbitkan 2020-01-01
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  2. 2
    Automatic differentiation of Grade I and II meningiomas on magnetic resonance image using an asymmetric convolutional neural network

    Automatic differentiation of Grade I and II meningiomas on magnetic resonance image using an asymmetric convolutional neural network oleh April Vassantachart, Yufeng Cao, Michael Gribble, Samuel Guzman, Jason C. Ye, Kyle Hurth, Anna Mathew, Gabriel Zada, Zhaoyang Fan, Eric L. Chang, Wensha Yang

    Diterbitkan 2022-03-01
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  3. 3
    Medulloblastoma uses GABA transaminase to survive in the cerebrospinal fluid microenvironment and promote leptomeningeal dissemination

    Medulloblastoma uses GABA transaminase to survive in the cerebrospinal fluid microenvironment and promote leptomeningeal dissemination oleh Vahan Martirosian, Krutika Deshpande, Hao Zhou, Keyue Shen, Kyle Smith, Paul Northcott, Michelle Lin, Vazgen Stepanosyan, Diganta Das, Jan Remsik, Danielle Isakov, Adrienne Boire, Henk De Feyter, Kyle Hurth, Shaobo Li, Joseph Wiemels, Brooke Nakamura, Ling Shao, Camelia Danilov, Thomas Chen, Josh Neman

    Diterbitkan 2021-07-01
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  4. 4
    Medulloblastoma uses GABA transaminase to survive in the cerebrospinal fluid microenvironment and promote leptomeningeal dissemination

    Medulloblastoma uses GABA transaminase to survive in the cerebrospinal fluid microenvironment and promote leptomeningeal dissemination oleh Vahan Martirosian, Krutika Deshpande, Hao Zhou, Keyue Shen, Kyle Smith, Paul Northcott, Michelle Lin, Vazgen Stepanosyan, Diganta Das, Jan Remsik, Danielle Isakov, Adrienne Boire, Henk De Feyter, Kyle Hurth, Shaobo Li, Joseph Wiemels, Brooke Nakamura, Ling Shao, Camelia Danilov, Thomas Chen, Josh Neman

    Diterbitkan 2021-06-01
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  5. 5
    Recurring homozygous ACTN2 variant (p.Arg506Gly) causes a recessive myopathy

    Recurring homozygous ACTN2 variant (p.Arg506Gly) causes a recessive myopathy oleh Sandra Donkervoort, Payam Mohassel, Melanie O'Leary, Devon E. Bonner, Taila Hartley, Nicole Acquaye, Astrid Brull, Tahseen Mozaffar, Mario A. Saporta, David A. Dyment, Jacinda B. Sampson, Sander Pajusalu, Christina Austin‐Tse, Kyle Hurth, Julie S. Cohen, Kirsty McWalter, Jodi Warman‐Chardon, Amy Crunk, A. Reghan Foley, Undiagnosed Diseases Network, Andrew L. Mammen, Matthew T. Wheeler, Anne O'Donnell‐Luria, Carsten G. Bönnemann

    Diterbitkan 2024-03-01
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