Hasil Pencarian - John Persing

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  1. 1
    Quasi steady-state hurricanes revisited

    Quasi steady-state hurricanes revisited oleh John Persing, Michael T. Montgomery, Roger K. Smith, James C. McWilliams

    Diterbitkan 2019-03-01
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  2. 2
    A Common Polymorphism within the IGF2 Imprinting Control Region Is Associated with Parent of Origin Specific Effects in Infantile Hemangiomas.

    A Common Polymorphism within the IGF2 Imprinting Control Region Is Associated with Parent of Origin Specific Effects in Infantile Hemangiomas. oleh Brent Schultz, Xiaopan Yao, Yanhong Deng, Milton Waner, Christopher Spock, Laura Tom, John Persing, Deepak Narayan

    Diterbitkan 2015-01-01
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  3. 3
    Generative Pre-Trained Transformers (GPT) Artificial intelligence – Assessing the Accuracy of ChatGPT as an Adjunct for Peri-operative Care

    Generative Pre-Trained Transformers (GPT) Artificial intelligence – Assessing the Accuracy of ChatGPT as an Adjunct for Peri-operative Care oleh Omar Allam, MD, Mica Williams, Mariana Almeida, David Alper, Andrew Craver, John Persing, MD, Michael Alperovich, MD, MSc

    Diterbitkan 2023-10-01
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  4. 4
    Abstract 19: Presence Of Psychiatric Diagnosis Negatively Impacts Patient-Reported Outcomes And Decreases Likelihood Of Autologous Reconstruction

    Abstract 19: Presence Of Psychiatric Diagnosis Negatively Impacts Patient-Reported Outcomes And Decreases Likelihood Of Autologous Reconstruction oleh Sumarth K. Mehta, BS, Amar H. Sheth, BS, Olamide Olawoyin, BS, Fouad Chouairi, BS, John Persing, MD, Michael Alperovich, MD, MSc

    Diterbitkan 2020-04-01
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  5. 5
    28. NATIONAL DISPARITIES IN MEDICAID ACCESS TO ORTHOTIC HELMET THERAPY FOR DEFORMATIONAL PLAGIOCEPHALY

    28. NATIONAL DISPARITIES IN MEDICAID ACCESS TO ORTHOTIC HELMET THERAPY FOR DEFORMATIONAL PLAGIOCEPHALY oleh Aaron Long, BS, Sacha Hauc, MPH, Alicia Stephan, BS, Adam Junn, BS, Jean Carlo Rivera, BS, Jacob Dinis, BS, Alexandra Junn, AB, John Persing, MD, Michael Alperovich, MD, MSc

    Diterbitkan 2022-04-01
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  6. 6
    1. Mutations in FOXI3 Cause Microtia and Craniofacial Microsomia

    1. Mutations in FOXI3 Cause Microtia and Craniofacial Microsomia oleh Andrew T. Timberlake, MD, PhD, Daniel Quiat, MD, Michael Cunningham, MD, John Persing, MD, Daniela V. Luquetti, MD, Carrie L. Heike, MD, Jonathan Seidman, PhD, Christine Seidman, PhD

    Diterbitkan 2023-05-01
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  7. 7
    130. De Novo Mutations in 555 Trios Implicate Chromatin Modification, Transcriptional Regulation, and Retinoic Acid Signaling in Syndromic Craniosynostosis

    130. De Novo Mutations in 555 Trios Implicate Chromatin Modification, Transcriptional Regulation, and Retinoic Acid Signaling in Syndromic Craniosynostosis oleh Andrew Timberlake, MD, PhD, Garrett Allington, BS, Emre Kiziltug, BS, Erin Wolfe, BS, John Persing, MD, Richard P. Lifton, MD, PhD, Gene Dx, Kristopher T. Kahle, MD, PhD

    Diterbitkan 2022-06-01
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  8. 8
    PC16. Mutations in FOXI3 Cause Microtia and Craniofacial Microsomia

    PC16. Mutations in FOXI3 Cause Microtia and Craniofacial Microsomia oleh Andrew T. Timberlake, MD, PhD, Daniel Quiat, MD, Michael L. Cunningham, MD, PhD, John Persing, MD, Daniela Luquetti, MD PhD, Carrie L. Heike, MD, Jonathan Seidman, PhD, Christine Seidman, PhD

    Diterbitkan 2023-04-01
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  9. 9
    Abstract QS54: What is the Difference Between Sagittal with Metopic and Isolated Sagittal Craniosynotosis? A Whole Brain Intrinsic Connectivity and Diffusion Tensor Imaging Study

    Abstract QS54: What is the Difference Between Sagittal with Metopic and Isolated Sagittal Craniosynotosis? A Whole Brain Intrinsic Connectivity and Diffusion Tensor Imaging Study oleh Raysa Cabrejo, BA, Cheryl Lacadie, B.S., Carolyn Chuang, MD, MHS, Jenny Yang, MD, MHS, Alexander Sun, BS, Eric Brooks, MD, MHS, Joel Beckett, MD, MHS, Kyle Gabrick, MD, Derek Steinbacher, DMD, MD, Michael Alperovich, MD, MSc, Kevin Pelphrey, PhD, Todd Constable, PhD, John Persing, MD

    Diterbitkan 2018-04-01
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  10. 10
    Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits

    Regulatory elements in SEM1-DLX5-DLX6 (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits oleh Paola Nicoletti, Samreen Zafer, Lital Matok, Inbar Irron, Meidva Patrick, Rotem Haklai, John Erol Evangelista, Giacomo B. Marino, Avi Ma’ayan, Anshuman Sewda, Greg Holmes, Sierra R. Britton, Won Jun Lee, Meng Wu, Ying Ru, Eric Arnaud, Lorenzo Botto, Lawrence C. Brody, Jo C. Byren, Michele Caggana, Suzan L. Carmichael, Deirdre Cilliers, Kristin Conway, Karen Crawford, Araceli Cuellar, Federico Di Rocco, Michael Engel, Jeffrey Fearon, Marcia L. Feldkamp, Richard Finnell, Sarah Fisher, Christian Freudlsperger, Gemma Garcia-Fructuoso, Rhinda Hagge, Yann Heuzé, Raymond J. Harshbarger, Charlotte Hobbs, Meredith Howley, Mary M. Jenkins, David Johnson, Cristina M. Justice, Alex Kane, Denise Kay, Arun Kumar Gosain, Peter Langlois, Laurence Legal-Mallet, Angela E. Lin, James L. Mills, Jenny E.V. Morton, Peter Noons, Andrew Olshan, John Persing, Julie M. Phipps, Richard Redett, Jennita Reefhuis, Elias Rizk, Thomas D. Samson, Gary M. Shaw, Robert Sicko, Nataliya Smith, David Staffenberg, Joan Stoler, Elizabeth Sweeney, Peter J. Taub, Andrew T. Timberlake, Jolanta Topczewska, Steven A. Wall, Alexander F. Wilson, Louise C. Wilson, Simeon A. Boyadjiev, Andrew O.M. Wilkie, Joan T. Richtsmeier, Ethylin Wang Jabs, Paul A. Romitti, David Karasik, Ramon Y. Birnbaum, Inga Peter

    Diterbitkan 2024-01-01
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