Resultats de la cerca - Matthew T. Whitehead

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  1. 1
    Physiologic Pineal Region, Choroid Plexus, and Dural Calcifications in the First Decade of Life

    Physiologic Pineal Region, Choroid Plexus, and Dural Calcifications in the First Decade of Life per Matthew T. Whitehead, Christopher C. Oh, Aditya Raju, Asim F. Choudhri

    Publicat 2014
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  2. 2
    3T Intraoperative MRI for Management of Pediatric CNS Neoplasms

    3T Intraoperative MRI for Management of Pediatric CNS Neoplasms per Asim F. Choudhri, Paul Klimo, Tyler S. Auschwitz, Matthew T. Whitehead, Frederick A. Boop

    Publicat 2014
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  3. 3
    Diffusion tensor imaging to guide surgical planning in intramedullary spinal cord tumors in children

    Diffusion tensor imaging to guide surgical planning in intramedullary spinal cord tumors in children per Asim F. Choudhri, Matthew T. Whitehead, Paul Klimo, Blake K. Montgomery, Frederick A. Boop

    Publicat 2014
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  4. 4
    Prevalence and Risk Factors for Pharmacoresistance in Children With Focal Cortical Dysplasia–Related Epilepsy

    Prevalence and Risk Factors for Pharmacoresistance in Children With Focal Cortical Dysplasia–Related Epilepsy per Nathan T. Cohen, Phat Chang, Xiaozhen You, Anqing Zhang, Kathryn Havens, Chima Oluigbo, Matthew T. Whitehead, Taha Gholipour, William D. Gaillard

    Publicat 2022
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  5. 5
    Magnetic resonance imaging spectrum of succinate dehydrogenase–related infantile leukoencephalopathy

    Magnetic resonance imaging spectrum of succinate dehydrogenase–related infantile leukoencephalopathy per Guy Helman, Ljubica Caldovic, Matthew T. Whitehead, Cas Simons, Knut Brockmann, Simon Edvardson, Renkui Bai, Isabella Moroni, J. Michael Taylor, Keith Van Haren, Ryan J. Taft, Adeline Vanderver, Marjo S. van der Knaap

    Publicat 2015
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  6. 6
    Refining the Neuroimaging Definition of the Dandy-Walker Phenotype

    Refining the Neuroimaging Definition of the Dandy-Walker Phenotype per Matthew T. Whitehead, Matthew J. Barkovich, Jai Sidpra, César Augusto Pinheiro Ferreira Alves, David M. Mirsky, Özgür Öztekin, Debarata Bhattacharya, Leandro Tavares Lucato, Sniya Sudhakar, Ajay Taranath, Savvas Andronikou, Sanjay P. Prabhu, Kimberly A. Aldinger, Parthiv Haldipur, Kathleen J. Millen, A. James Barkovich, Eugen Boltshauser, William B. Dobyns, Kshitij Mankad

    Publicat 2022
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  7. 7
    Loss-of-Function Alanyl-tRNA Synthetase Mutations Cause an Autosomal-Recessive Early-Onset Epileptic Encephalopathy with Persistent Myelination Defect

    Loss-of-Function Alanyl-tRNA Synthetase Mutations Cause an Autosomal-Recessive Early-Onset Epileptic Encephalopathy with Persistent Myelination Defect per Cas Simons, Laurie B. Griffin, Guy Helman, Gretchen Golas, Amy Pizzino, Miriam Bloom, Jennifer L. Murphy, Joanna Crawford, Sarah Helen Evans, Scott Topper, Matthew T. Whitehead, John M. Schreiber, Kimberly A. Chapman, Cyndi Tifft, Katrina B. Lu, Howard Gamper, Megumi Shigematsu, Ryan J. Taft, Anthony Antonellis, Ya‐Ming Hou, Adeline Vanderver

    Publicat 2015
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  8. 8
    ACR Appropriateness Criteria ® Cerebrovascular Disease

    ACR Appropriateness Criteria ® Cerebrovascular Disease per Michael B. Salmela, Shabnam Mortazavi, Bharathi Jagadeesan, Daniel F. Broderick, Judah Burns, Tejaswini Deshmukh, H. Benjamin Harvey, Jenny K. Hoang, Christopher H. Hunt, Tabassum A. Kennedy, Alexander A. Khalessi, William J. Mack, Nandini D. Patel, Joel S. Perlmutter, Bruno Policeni, Jason W. Schroeder, Gavin Setzen, Matthew T. Whitehead, Rebecca S. Cornelius, Amanda S. Corey

    Publicat 2017
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  9. 9
    ACR Appropriateness Criteria® Suspected Spine Trauma-Child

    ACR Appropriateness Criteria® Suspected Spine Trauma-Child per Nadja Kadom, Susan Palasis, Sumit Pruthi, Walter L. Biffl, Timothy N. Booth, Nilesh Desai, Richard A. Falcone, Jeremy Jones, Madeline Joseph, Abhaya V. Kulkarni, Jennifer R. Marín, Sarah Sarvis Milla, David M. Mirsky, John S. Myseros, Charles A. Reitman, Richard L. Robertson, Maura E. Ryan, Gaurav Saigal, Jacob F. Schulz, Bruno P. Soares, Aylin Tekes, Andrew T. Trout, Matthew T. Whitehead, Boaz Karmazyn

    Publicat 2019
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  10. 10
    The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders

    The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders per Jai Sidpra, Sniya Sudhakar, Asthik Biswas, Flavia Massey, Valentina Turchetti, Tracy Lau, Edward Cook, Javeria Raza Alvi, Hasnaa M. Elbendary, Jerry Jewell, Antonella Riva, Alessandro Orsini, Aglaia Vignoli, Zara Federico, Jessica Rosenblum, An‐Sofie Schoonjans, Matthias De Wachter, Ignacio Delgado Alvarez, Ana Felipe‐Rucián, Nourelhoda A. Haridy, Shahzad Haider, Mashaya Zaman, Selina Banu, Najwa Anwaar, Fatima Rahman, Shazia Maqbool, Rashmi Yadav, Vincenzo Salpietro, Reza Maroofian, Rajan Patel, Rupa Radhakrishnan, Sanjay P. Prabhu, Klaske D. Lichtenbelt, Helen Stewart, Yoshiko Murakami, Ulrike Löbel, Felice D’Arco, Emma Wakeling, Wendy D. Jones, Eleanor Hay, Sanjay Bhate, Thomas S. Jacques, David M. Mirsky, Matthew T. Whitehead, Maha S. Zaki, Tipu Sultan, Pasquale Striano, Anna Jansen, Maarten H. Lequin, Linda S. de Vries, Mariasavina Severino, Andrew C. Edmondson, Lara Menzies, Philippe M. Campeau, Henry Houlden, Amy McTague, Stéphanie Efthymiou, Kshitij Mankad

    Publicat 2024
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